The distribution of callose synthase, cellulose synthase, and sucrose synthase in tobacco pollen tubes is controlled by actin filaments and microtubules in different ways. Cellulose synthase is present along the entire length of pollen tubes, with higher concentration at the apex, while callose synthase is located in the apex and around callose plugs. Actin filaments and endomembrane dynamics control the distribution of both enzymes by transporting them via Golgi bodies and vesicles. Microtubules control the positioning of callose synthase in distal regions and around plugs, but only partially influence cellulose synthase distribution. Sucrose synthase binds to actin filaments and provides UDP-
describe cell cycle and cell cycle control system for downloading the presentation , more presentations , infographics and blogs visit :
studyscienceblog.wordpress.com
This presentation provides an overview of cell division, including mitosis and meiosis. It defines the cell and cell cycle, describing the stages of interphase and mitosis. There are two main types of cell division - mitosis, which produces identical daughter cells, and meiosis, which reduces chromosome number by half to produce gametes. The stages of each type of division are explained in detail. Key differences between mitosis and meiosis are outlined. In conclusion, cell division is explained as essential for growth, development, and reproduction in organisms.
The document discusses cell division, specifically mitosis and meiosis. Mitosis produces genetically identical daughter cells and is used for growth and repair. Meiosis produces haploid gametes through two cell divisions and leads to genetic variation in offspring. The cell cycle consists of interphase and mitosis. Interphase includes DNA replication and cell growth. Mitosis separates the duplicated chromosomes into two daughter nuclei.
The document discusses the mechanism of cell division in eukaryotic cells. It describes the four main phases of the cell cycle - growth, DNA synthesis, nuclear division through mitosis, and cytokinesis. The S phase involves DNA replication, while the M phase comprises mitosis and cytokinesis. Mitosis is further broken down into the prophase, metaphase, anaphase and telophase stages. Cytokinesis then divides the cytoplasm, resulting in two daughter cells each with identical DNA to the original parent cell. The cell cycle is tightly regulated by control proteins to ensure proper division.
The document discusses cell division (mitosis) and the cell cycle. It describes the main stages of the cell cycle as interphase (which includes G1, S, and G2 phases) and mitosis, followed by cytokinesis. Mitosis is then explained in more detail, outlining the four phases of prophase, metaphase, anaphase and telophase. It states that mitosis produces two genetically identical daughter cells and is involved in processes like growth, development, and asexual reproduction. The document also mentions that tumors are caused by uncontrolled cell division, which can occur in any tissue or organ.
The document discusses several studies on the cell cycle and cell division. It describes how small signaling molecules like c-di-GMP act as a control switch to allow cells to progress through different phases of the cell cycle. Another study found that dividing cells do not always add the same amount of mass before dividing, challenging previous conclusions. Understanding how cells control and regulate division is important for learning about related pathologies like cancer. Further discovery of molecules involved in the cell cycle process could help repair defects and potentially lead to cures.
The document discusses the structure and function of mitochondria. Key points include:
- Mitochondria are known as the "powerhouse of the cell" as they help process nutrients to release energy. They are found in high concentrations in muscle cells requiring more energy.
- Mitochondria are enclosed in two membranes - an outer membrane and inner membrane, with space between called the intermembrane space.
- The inner membrane is more complex and contains electron transport chain and ATP synthase complexes. It is selectively permeable.
This document discusses differential cell affinity and the differential adhesion hypothesis. It explains that during development, cells show selective affinity for similar cell types over dissimilar types. This is due to cell adhesion molecules that allow cells to stick together. The differential adhesion hypothesis proposes that cells will actively move to create tissue organization based on their differing adhesion strengths - arranging themselves into the most thermodynamically stable pattern. Cells with stronger adhesion to their own type will cluster together, while cells with weaker adhesion between types will sort apart. Changes in gene activity can alter cell adhesion molecules and cause cellular movements to restore equilibrium.
describe cell cycle and cell cycle control system for downloading the presentation , more presentations , infographics and blogs visit :
studyscienceblog.wordpress.com
This presentation provides an overview of cell division, including mitosis and meiosis. It defines the cell and cell cycle, describing the stages of interphase and mitosis. There are two main types of cell division - mitosis, which produces identical daughter cells, and meiosis, which reduces chromosome number by half to produce gametes. The stages of each type of division are explained in detail. Key differences between mitosis and meiosis are outlined. In conclusion, cell division is explained as essential for growth, development, and reproduction in organisms.
The document discusses cell division, specifically mitosis and meiosis. Mitosis produces genetically identical daughter cells and is used for growth and repair. Meiosis produces haploid gametes through two cell divisions and leads to genetic variation in offspring. The cell cycle consists of interphase and mitosis. Interphase includes DNA replication and cell growth. Mitosis separates the duplicated chromosomes into two daughter nuclei.
The document discusses the mechanism of cell division in eukaryotic cells. It describes the four main phases of the cell cycle - growth, DNA synthesis, nuclear division through mitosis, and cytokinesis. The S phase involves DNA replication, while the M phase comprises mitosis and cytokinesis. Mitosis is further broken down into the prophase, metaphase, anaphase and telophase stages. Cytokinesis then divides the cytoplasm, resulting in two daughter cells each with identical DNA to the original parent cell. The cell cycle is tightly regulated by control proteins to ensure proper division.
The document discusses cell division (mitosis) and the cell cycle. It describes the main stages of the cell cycle as interphase (which includes G1, S, and G2 phases) and mitosis, followed by cytokinesis. Mitosis is then explained in more detail, outlining the four phases of prophase, metaphase, anaphase and telophase. It states that mitosis produces two genetically identical daughter cells and is involved in processes like growth, development, and asexual reproduction. The document also mentions that tumors are caused by uncontrolled cell division, which can occur in any tissue or organ.
The document discusses several studies on the cell cycle and cell division. It describes how small signaling molecules like c-di-GMP act as a control switch to allow cells to progress through different phases of the cell cycle. Another study found that dividing cells do not always add the same amount of mass before dividing, challenging previous conclusions. Understanding how cells control and regulate division is important for learning about related pathologies like cancer. Further discovery of molecules involved in the cell cycle process could help repair defects and potentially lead to cures.
The document discusses the structure and function of mitochondria. Key points include:
- Mitochondria are known as the "powerhouse of the cell" as they help process nutrients to release energy. They are found in high concentrations in muscle cells requiring more energy.
- Mitochondria are enclosed in two membranes - an outer membrane and inner membrane, with space between called the intermembrane space.
- The inner membrane is more complex and contains electron transport chain and ATP synthase complexes. It is selectively permeable.
This document discusses differential cell affinity and the differential adhesion hypothesis. It explains that during development, cells show selective affinity for similar cell types over dissimilar types. This is due to cell adhesion molecules that allow cells to stick together. The differential adhesion hypothesis proposes that cells will actively move to create tissue organization based on their differing adhesion strengths - arranging themselves into the most thermodynamically stable pattern. Cells with stronger adhesion to their own type will cluster together, while cells with weaker adhesion between types will sort apart. Changes in gene activity can alter cell adhesion molecules and cause cellular movements to restore equilibrium.
International Journal of Stem Cell Research and Transplantation (IJST) is a peer-reviewed journal, and is dedicated to providing information with respect to the latest advancements that are being upgraded in our everyday life with respect to the application of Stem cells.
International Journal of Stem Cell Research and Transplantation (IJST) ISSN:2328-3548, is a free, Open Access, Peer-reviewed, exclusive online journal covering areas of Stem cell research, translational work and Clinical studies in the specialty of Stem Cells and Transplantation including allied specialties relevant to the core subject, which is dedicated in publishing high quality manuscripts.
International Journal of Stem Cell Research and Transplantation (IJST) is an international, Open Access, peer-reviewed journal, which mainly focuses, on the advancements made in the field of cell biology, specifically in the field of Stem Cells.
Eukaryotic cells have a nucleus surrounded by a nuclear membrane, contain organelles like mitochondria and chloroplasts, and are generally larger than prokaryotic cells. Prokaryotic cells lack a nucleus and most organelles, have only a single chromosome, and are generally unicellular. Key differences include eukaryotic cells having a nucleus with a nuclear membrane, multiple chromosomes, organelles like mitochondria and chloroplasts, and being generally larger and multicellular compared to prokaryotic cells which lack most organelles and a nucleus.
This document discusses the key structures and traits of cells. It describes two main types of cells - prokaryotic cells which lack membrane-bound structures and eukaryotic cells which have structures like the nucleus enclosed in membranes. The document outlines several organelles common to both plant and animal cells, including the cell membrane, cytoplasm, cytoskeleton, nucleus, and nuclear membrane. It provides examples of the different types of cells and explains the basic functions of the main cell structures.
The document discusses cell division and genetics. It explains that cell division, through mitosis and meiosis, allows for the transmission of genetic material from parent cells to daughter cells. Mitosis produces two identical daughter cells during normal cell growth and reproduction. Meiosis reduces the chromosome number by half and produces genetic variation through independent assortment and crossing over, resulting in gametes for sexual reproduction.
Eukaryotic cells are defined by several key features, including a membrane-bound nucleus that contains DNA packaged into chromosomes. Eukaryotic cells also contain membrane-bound organelles such as mitochondria, the endoplasmic reticulum, Golgi apparatus, lysosomes, and peroxisomes. The endoplasmic reticulum packages and transports proteins while the Golgi apparatus processes them, and lysosomes contain enzymes to break down waste. Eukaryotic cells may be single-celled microorganisms or part of multicellular organisms, and their DNA is organized into linear chromosomes within the nucleus.
This document outlines the establishment of a stem cell research chair at King Abdulaziz University from 2009-2015. It begins with the author attending a knee surgery course in 2009 where he learned about cartilage regeneration techniques. He then proposed creating a research chair to RACI in 2010, which involved a lengthy approval process. He built up a research team of professors and clinicians from various specialties. Research projects focused on isolating and characterizing mesenchymal stem cells, cartilage regeneration, and animal studies on rabbits. The chair fulfilled regulatory requirements like submitting annual reports and had an organizational structure to oversee the research groups.
Mammalian MSC from Selected Species: Features and Applications
Christiane Uder, Sandra Br€uckner, Sandra Winkler, Hans-Michael Tautenhahn,†‡ Bruno Christ†*
Mesenchymal stromal/stem cells (MSC) are promising candidates for cellular therapy of different diseases in humans and in animals. Following the guidelines of the International Society for Cell Therapy, human MSC may be identified by expression of a specific panel of cell surface markers (CD1051, CD731, CD901, CD34-, CD14-, or CD11b-, CD79- or CD19-, HLA-DR-). In addition, multiple differentiation potential into at least the osteogenic, adipogenic, and chondrogenic lineage is a main criterion for MSC definition. Human MSC and MSC of a variety of mammals isolated from different tissues meet these criteria. In addition to the abovementioned, they express many more cell surface markers. Yet, these are not uniquely expressed by MSC. The gross phenotypic appearance like marker expression and differentiation potential is similar albeit not identical for MSC from different tissues and species. Similarly, MSC may feature different biological characteristics depending on the tissue source and the isolation and culture procedures. Their versatile biological qualities comprising immunomodulatory, anti-inflammatory, and proregenerative capacities rely largely on the migratory and secretory capabilities of MSC. They are attracted to sites of tissue lesion and secrete factors to promote self-repair of the injured tissue. This is a big perspective for clinical MSC applications in both veterinary and human medicine. Phase I/II clinical trials have been initiated to assess safety and feasibility of MSC therapies in acute and chronic disease settings. Yet, since the mode of MSC action in a specific disease environment is still unknown at large, it is mandatory to unravel the response of MSC from a given source onto a specific disease environment in suitable animal models prior to clinical applications.
This document summarizes the role of Notch signaling in intestinal homeostasis and cancer. It discusses:
1) Notch signaling balances intestinal stem cell self-renewal and differentiation, maintaining homeostasis of the intestinal epithelium.
2) In the intestine, stem cells in the crypts fuel continuous production of differentiated cell types that move up the villi. Notch signaling controls this process.
3) Dysregulation of Notch is involved in intestinal cancer, as it controls lateral inhibition between stem cells and their differentiation.
This document compares and contrasts prokaryotic and eukaryotic cells. It notes that prokaryotes like bacteria and archaea lack complex internal structures like membrane-bound organelles, while eukaryotic cells have structures like the nucleus enclosed in membranes. A key difference is that prokaryotes have 70S ribosomes while eukaryotes have 80S ribosomes in the cytoplasm and 70S in organelles. The endosymbiotic theory proposes that mitochondria and chloroplasts were originally prokaryotic cells that lived symbiotically inside eukaryotic cells and became permanent organelles.
This document summarizes key aspects of cell biology. It defines the cell and compares prokaryotic and eukaryotic cells. It describes several important cell organelles - plastids, the nucleus, mitochondria, the Golgi apparatus, and the endoplasmic reticulum. It also summarizes the cell theory, which states that cells are the fundamental unit of life and that new cells are produced from existing cells.
The document summarizes key aspects of cell walls and endoplasmic reticulum. It describes how cell walls originate from the phragmoplast and are composed mainly of cellulose, hemicellulose, pectin, and lignin. Cell walls are differentiated into the middle lamella, primary cell wall, and secondary cell wall. Endoplasmic reticulum forms a network of tubules and vesicles that traverse the cytoplasmic matrix. It has smooth and rough forms, functions in transport, storage, synthesis of molecules, and provides structural support to the cell.
The document summarizes cell division and the two main types: mitosis and meiosis. Mitosis produces two identical daughter cells and is used for growth, repair, and replacement of somatic cells. It involves the phases of interphase, prophase, metaphase, anaphase, telophase, and cytokinesis. Meiosis produces four non-identical gamete cells through two rounds of division and is involved in sexual reproduction.
This document discusses biomaterials inspired by the extracellular matrix (ECM). It defines biomimicry, bioinspiration and bioderivation as three paradigms for learning from biological systems. The document then describes three main types of ECM mimicry in biomaterials: 1) mimicking ECM functions by using ECM components, either through direct copying or partial copying, 2) mimicking ECM architecture and topography through hierarchical microstructure and topographical features, and 3) mimicking ECM protein design and assembly. The goal is to create biomaterials that interact with cells in similar ways to the native ECM environment.
Autophagy is a process where cells deliver cytoplasmic components and organelles to lysosomes for degradation. It plays an important role in development, nutrient deprivation, and aging. Recent evidence suggests autophagy is key to how caloric restriction and mutations in insulin signaling can promote longevity. Autophagy helps maintain cellular homeostasis and removes damaged organelles, likely contributing to longevity by reducing free radical production over time. It is regulated by the target of rapamycin (TOR) pathway and other molecular machinery that are highly conserved from yeast to humans.
Intra_articular injection of synovial mesenchymal stem cells improves cartila...Christina Jablonski
This study found that injecting mesenchymal stem cells (MSCs) from the synovial membrane improved cartilage repair in a mouse cartilage injury model. MSCs from both the healing MRL mouse strain and the non-healing C57BL6 mouse strain promoted increased cartilage repair when injected into injured C57BL6 mice. While MRL MSCs were observed at the injury site 2 weeks after injection, C57BL6 MSCs were not observed. This suggests that synovial MSCs, regardless of mouse strain, can have beneficial effects on cartilage repair when injected into an injured joint.
This document summarizes the biology and potential clinical applications of mesenchymal stem cells (MSCs) derived from the Wharton's jelly of the umbilical cord. It discusses how MSCs were originally isolated from bone marrow but umbilical cord is now seen as a promising alternative source due to its abundance of MSCs and the non-invasive collection method. MSCs from Wharton's jelly (WJ-MSCs) share properties with bone marrow MSCs yet are considered more primitive. The review examines the multilineage potential and immunomodulatory abilities of WJ-MSCs and their emerging roles in treating cancer, graft-versus-host disease, and systemic lupus erythemat
This document provides an overview of cell reproduction through mitosis and meiosis. It discusses the importance of cell reproduction for growth, maintenance and repair. The key differences between mitosis and meiosis are outlined, including that mitosis produces two identical daughter cells while meiosis produces four non-identical daughter cells each with half the number of chromosomes. The stages of the cell cycle and phases of mitosis and meiosis are defined in detail including prophase, metaphase, anaphase and telophase. Gametogenesis is also summarized as the formation of sperm and egg cells through spermatogenesis and oogenesis respectively.
This document discusses the structure of eukaryotic cells. It defines eukaryotic cells as having a membrane-bound nucleus and lists some of their key organelles like the plasma membrane, nucleus, mitochondria, Golgi bodies, lysosomes, endoplasmic reticulum, peroxisomes, chloroplasts, cytoskeleton, and vacuoles. It describes the functions of these organelles like the nucleus containing genetic material, mitochondria generating energy, and vacuoles storing waste. The document provides a high-level overview of the anatomy of eukaryotic cells.
As part of a group Management of Promotions assignment, another classmate and I created a marketing plan for Edible Arrangements. The project was evenly divided with each team member creating the content for a specified number of sections.
The document discusses prototyping and provides examples of different types of prototypes including paper prototypes, digital prototypes, storyboards, role plays, and space prototypes. It explains that prototyping is used to make ideas tangible and test reactions from users in order to gain insights. Prototypes should be iterated on and fail early to push ideas further and save time and money. Both low and high fidelity prototypes are mentioned as ways to test ideas at different stages of the design process.
International Journal of Stem Cell Research and Transplantation (IJST) is a peer-reviewed journal, and is dedicated to providing information with respect to the latest advancements that are being upgraded in our everyday life with respect to the application of Stem cells.
International Journal of Stem Cell Research and Transplantation (IJST) ISSN:2328-3548, is a free, Open Access, Peer-reviewed, exclusive online journal covering areas of Stem cell research, translational work and Clinical studies in the specialty of Stem Cells and Transplantation including allied specialties relevant to the core subject, which is dedicated in publishing high quality manuscripts.
International Journal of Stem Cell Research and Transplantation (IJST) is an international, Open Access, peer-reviewed journal, which mainly focuses, on the advancements made in the field of cell biology, specifically in the field of Stem Cells.
Eukaryotic cells have a nucleus surrounded by a nuclear membrane, contain organelles like mitochondria and chloroplasts, and are generally larger than prokaryotic cells. Prokaryotic cells lack a nucleus and most organelles, have only a single chromosome, and are generally unicellular. Key differences include eukaryotic cells having a nucleus with a nuclear membrane, multiple chromosomes, organelles like mitochondria and chloroplasts, and being generally larger and multicellular compared to prokaryotic cells which lack most organelles and a nucleus.
This document discusses the key structures and traits of cells. It describes two main types of cells - prokaryotic cells which lack membrane-bound structures and eukaryotic cells which have structures like the nucleus enclosed in membranes. The document outlines several organelles common to both plant and animal cells, including the cell membrane, cytoplasm, cytoskeleton, nucleus, and nuclear membrane. It provides examples of the different types of cells and explains the basic functions of the main cell structures.
The document discusses cell division and genetics. It explains that cell division, through mitosis and meiosis, allows for the transmission of genetic material from parent cells to daughter cells. Mitosis produces two identical daughter cells during normal cell growth and reproduction. Meiosis reduces the chromosome number by half and produces genetic variation through independent assortment and crossing over, resulting in gametes for sexual reproduction.
Eukaryotic cells are defined by several key features, including a membrane-bound nucleus that contains DNA packaged into chromosomes. Eukaryotic cells also contain membrane-bound organelles such as mitochondria, the endoplasmic reticulum, Golgi apparatus, lysosomes, and peroxisomes. The endoplasmic reticulum packages and transports proteins while the Golgi apparatus processes them, and lysosomes contain enzymes to break down waste. Eukaryotic cells may be single-celled microorganisms or part of multicellular organisms, and their DNA is organized into linear chromosomes within the nucleus.
This document outlines the establishment of a stem cell research chair at King Abdulaziz University from 2009-2015. It begins with the author attending a knee surgery course in 2009 where he learned about cartilage regeneration techniques. He then proposed creating a research chair to RACI in 2010, which involved a lengthy approval process. He built up a research team of professors and clinicians from various specialties. Research projects focused on isolating and characterizing mesenchymal stem cells, cartilage regeneration, and animal studies on rabbits. The chair fulfilled regulatory requirements like submitting annual reports and had an organizational structure to oversee the research groups.
Mammalian MSC from Selected Species: Features and Applications
Christiane Uder, Sandra Br€uckner, Sandra Winkler, Hans-Michael Tautenhahn,†‡ Bruno Christ†*
Mesenchymal stromal/stem cells (MSC) are promising candidates for cellular therapy of different diseases in humans and in animals. Following the guidelines of the International Society for Cell Therapy, human MSC may be identified by expression of a specific panel of cell surface markers (CD1051, CD731, CD901, CD34-, CD14-, or CD11b-, CD79- or CD19-, HLA-DR-). In addition, multiple differentiation potential into at least the osteogenic, adipogenic, and chondrogenic lineage is a main criterion for MSC definition. Human MSC and MSC of a variety of mammals isolated from different tissues meet these criteria. In addition to the abovementioned, they express many more cell surface markers. Yet, these are not uniquely expressed by MSC. The gross phenotypic appearance like marker expression and differentiation potential is similar albeit not identical for MSC from different tissues and species. Similarly, MSC may feature different biological characteristics depending on the tissue source and the isolation and culture procedures. Their versatile biological qualities comprising immunomodulatory, anti-inflammatory, and proregenerative capacities rely largely on the migratory and secretory capabilities of MSC. They are attracted to sites of tissue lesion and secrete factors to promote self-repair of the injured tissue. This is a big perspective for clinical MSC applications in both veterinary and human medicine. Phase I/II clinical trials have been initiated to assess safety and feasibility of MSC therapies in acute and chronic disease settings. Yet, since the mode of MSC action in a specific disease environment is still unknown at large, it is mandatory to unravel the response of MSC from a given source onto a specific disease environment in suitable animal models prior to clinical applications.
This document summarizes the role of Notch signaling in intestinal homeostasis and cancer. It discusses:
1) Notch signaling balances intestinal stem cell self-renewal and differentiation, maintaining homeostasis of the intestinal epithelium.
2) In the intestine, stem cells in the crypts fuel continuous production of differentiated cell types that move up the villi. Notch signaling controls this process.
3) Dysregulation of Notch is involved in intestinal cancer, as it controls lateral inhibition between stem cells and their differentiation.
This document compares and contrasts prokaryotic and eukaryotic cells. It notes that prokaryotes like bacteria and archaea lack complex internal structures like membrane-bound organelles, while eukaryotic cells have structures like the nucleus enclosed in membranes. A key difference is that prokaryotes have 70S ribosomes while eukaryotes have 80S ribosomes in the cytoplasm and 70S in organelles. The endosymbiotic theory proposes that mitochondria and chloroplasts were originally prokaryotic cells that lived symbiotically inside eukaryotic cells and became permanent organelles.
This document summarizes key aspects of cell biology. It defines the cell and compares prokaryotic and eukaryotic cells. It describes several important cell organelles - plastids, the nucleus, mitochondria, the Golgi apparatus, and the endoplasmic reticulum. It also summarizes the cell theory, which states that cells are the fundamental unit of life and that new cells are produced from existing cells.
The document summarizes key aspects of cell walls and endoplasmic reticulum. It describes how cell walls originate from the phragmoplast and are composed mainly of cellulose, hemicellulose, pectin, and lignin. Cell walls are differentiated into the middle lamella, primary cell wall, and secondary cell wall. Endoplasmic reticulum forms a network of tubules and vesicles that traverse the cytoplasmic matrix. It has smooth and rough forms, functions in transport, storage, synthesis of molecules, and provides structural support to the cell.
The document summarizes cell division and the two main types: mitosis and meiosis. Mitosis produces two identical daughter cells and is used for growth, repair, and replacement of somatic cells. It involves the phases of interphase, prophase, metaphase, anaphase, telophase, and cytokinesis. Meiosis produces four non-identical gamete cells through two rounds of division and is involved in sexual reproduction.
This document discusses biomaterials inspired by the extracellular matrix (ECM). It defines biomimicry, bioinspiration and bioderivation as three paradigms for learning from biological systems. The document then describes three main types of ECM mimicry in biomaterials: 1) mimicking ECM functions by using ECM components, either through direct copying or partial copying, 2) mimicking ECM architecture and topography through hierarchical microstructure and topographical features, and 3) mimicking ECM protein design and assembly. The goal is to create biomaterials that interact with cells in similar ways to the native ECM environment.
Autophagy is a process where cells deliver cytoplasmic components and organelles to lysosomes for degradation. It plays an important role in development, nutrient deprivation, and aging. Recent evidence suggests autophagy is key to how caloric restriction and mutations in insulin signaling can promote longevity. Autophagy helps maintain cellular homeostasis and removes damaged organelles, likely contributing to longevity by reducing free radical production over time. It is regulated by the target of rapamycin (TOR) pathway and other molecular machinery that are highly conserved from yeast to humans.
Intra_articular injection of synovial mesenchymal stem cells improves cartila...Christina Jablonski
This study found that injecting mesenchymal stem cells (MSCs) from the synovial membrane improved cartilage repair in a mouse cartilage injury model. MSCs from both the healing MRL mouse strain and the non-healing C57BL6 mouse strain promoted increased cartilage repair when injected into injured C57BL6 mice. While MRL MSCs were observed at the injury site 2 weeks after injection, C57BL6 MSCs were not observed. This suggests that synovial MSCs, regardless of mouse strain, can have beneficial effects on cartilage repair when injected into an injured joint.
This document summarizes the biology and potential clinical applications of mesenchymal stem cells (MSCs) derived from the Wharton's jelly of the umbilical cord. It discusses how MSCs were originally isolated from bone marrow but umbilical cord is now seen as a promising alternative source due to its abundance of MSCs and the non-invasive collection method. MSCs from Wharton's jelly (WJ-MSCs) share properties with bone marrow MSCs yet are considered more primitive. The review examines the multilineage potential and immunomodulatory abilities of WJ-MSCs and their emerging roles in treating cancer, graft-versus-host disease, and systemic lupus erythemat
This document provides an overview of cell reproduction through mitosis and meiosis. It discusses the importance of cell reproduction for growth, maintenance and repair. The key differences between mitosis and meiosis are outlined, including that mitosis produces two identical daughter cells while meiosis produces four non-identical daughter cells each with half the number of chromosomes. The stages of the cell cycle and phases of mitosis and meiosis are defined in detail including prophase, metaphase, anaphase and telophase. Gametogenesis is also summarized as the formation of sperm and egg cells through spermatogenesis and oogenesis respectively.
This document discusses the structure of eukaryotic cells. It defines eukaryotic cells as having a membrane-bound nucleus and lists some of their key organelles like the plasma membrane, nucleus, mitochondria, Golgi bodies, lysosomes, endoplasmic reticulum, peroxisomes, chloroplasts, cytoskeleton, and vacuoles. It describes the functions of these organelles like the nucleus containing genetic material, mitochondria generating energy, and vacuoles storing waste. The document provides a high-level overview of the anatomy of eukaryotic cells.
As part of a group Management of Promotions assignment, another classmate and I created a marketing plan for Edible Arrangements. The project was evenly divided with each team member creating the content for a specified number of sections.
The document discusses prototyping and provides examples of different types of prototypes including paper prototypes, digital prototypes, storyboards, role plays, and space prototypes. It explains that prototyping is used to make ideas tangible and test reactions from users in order to gain insights. Prototypes should be iterated on and fail early to push ideas further and save time and money. Both low and high fidelity prototypes are mentioned as ways to test ideas at different stages of the design process.
This document outlines 50 essential content marketing hacks presented by Matt Heinz, President of Heinz Marketing Inc. at CMWorld. It provides an agenda for the presentation and covers topics such as content planning, measurement, formats, distribution, influencer engagement, repurposing content, and getting sales teams to leverage content. The goal is to provide new tools, tricks and best practices to help convert readers into customers through effective content marketing.
20 Ideas for your Website Homepage ContentBarry Feldman
Perplexed about what to put on your website home? Every company deals with this tough challenge. The 20 ideas in this presentation should give you a strong starting point.
10 Insightful Quotes On Designing A Better Customer ExperienceYuan Wang
In an ever-changing landscape of one digital disruption after another, companies and organisations are looking for new ways to understand their target markets and engage them better. Increasingly they invest in user experience (UX) and customer experience design (CX) capabilities by working with a specialist UX agency or developing their own UX lab. Some UX practitioners are touting leaner and faster ways of developing customer-centric products and services, via methodologies such as guerilla research, rapid prototyping and Agile UX. Others seek innovation and fulfilment by spending more time in research, being more inclusive, and designing for social goods.
Experience is more than just an interface. It is a relationship, as well as a series of touch points between your brand and your customer. Here are our top 10 highlights and takeaways from the recent UX Australia conference to help you transform your customer experience design.
For full article, continue reading at https://yump.com.au/10-ways-supercharge-customer-experience-design/
The document discusses how personalization and dynamic content are becoming increasingly important on websites. It notes that 52% of marketers see content personalization as critical and 75% of consumers like it when brands personalize their content. However, personalization can create issues for search engine optimization as dynamic URLs and content are more difficult for search engines to index than static pages. The document provides tips for SEOs to help address these personalization and SEO challenges, such as using static URLs when possible and submitting accurate sitemaps.
How to Build a Dynamic Social Media PlanPost Planner
Stop guessing and wasting your time on networks and strategies that don’t work!
Join Rebekah Radice and Katie Lance to learn how to optimize your social networks, the best kept secrets for hot content, top time management tools, and much more!
Watch the replay here: bit.ly/socialmedia-plan
Artificial intelligence (AI) is everywhere, promising self-driving cars, medical breakthroughs, and new ways of working. But how do you separate hype from reality? How can your company apply AI to solve real business problems?
Here’s what AI learnings your business should keep in mind for 2017.
Study: The Future of VR, AR and Self-Driving CarsLinkedIn
We asked LinkedIn members worldwide about their levels of interest in the latest wave of technology: whether they’re using wearables, and whether they intend to buy self-driving cars and VR headsets as they become available. We asked them too about their attitudes to technology and to the growing role of Artificial Intelligence (AI) in the devices that they use. The answers were fascinating – and in many cases, surprising.
This SlideShare explores the full results of this study, including detailed market-by-market breakdowns of intention levels for each technology – and how attitudes change with age, location and seniority level. If you’re marketing a tech brand – or planning to use VR and wearables to reach a professional audience – then these are insights you won’t want to miss.
Practical manual of in vitro fertilizationSpringer
Cumulus cells surround oocytes in the ovaries and have essential functions in supporting oocyte growth and maturation. They are closely connected to the oocyte and allow for exchange of molecules between the cells. Several studies have analyzed gene expression in cumulus cells and found differences associated with oocyte quality - some genes were expressed more or less in cumulus cells surrounding higher-quality oocytes. This suggests it may be possible to assess oocyte potential noninvasively by analyzing gene expression in surrounding cumulus cells.
This document summarizes the roles of actin and microtubules in endocytosis across different organisms. It discusses how actin nucleation at endocytic sites drives vesicle formation in yeast and animals. Actin filaments also transport internalized vesicles within cells, while microtubules facilitate long-range transport of endosomes in mammalian cells. In plants, actin is important for long-range trafficking of vesicles, while both cortical and endoplasmic microtubules are involved in endocytic processes in dividing and non-dividing cells respectively. Thus endocytosis relies on dynamic interactions between the cytoskeleton and membranes that vary across kingdoms but share some conserved features.
Building a plant cell wall at a glance.pdflizette89
This document summarizes the key components of plant cell walls and how they are synthesized and assembled. Plant cell walls are composed of cellulose microfibrils cross-linked by hemicelluloses and pectins. These components include cellulose, callose, pectins, xyloglucans, and xylans. They are synthesized in the Golgi and plasma membrane by glycosyltransferases and cellulose synthases and transported to the cell wall. Proper assembly of the cell wall components is essential for determining plant growth, shape and mechanical strength.
1) The document presents a new method for synchronizing proliferating mammalian cells in the G1 phase of the cell cycle using standard optical flow cytometry to separate cells by size.
2) Current methods for synchronizing cells rely on chemical agents that arrest the cell cycle, which can introduce unwanted variables and decouple cell growth from the cell cycle.
3) The new method exploits the correlation between cell size and age, sorting for the smallest cells using light scattering parameters as a proxy for size, which yields a highly purified population of over 90% G1 cells without chemical treatment.
It has long been assumed that the individual cisternal stacks that comprise the plant Golgi apparatus multiply
by some kind of fission process. However, more recently, it has been demonstrated that the Golgi apparatus
can be experimentally disassembled and the reformation process from the ER (endoplasmic reticulum)
monitored sequentially using confocal fluorescence and electron microscopy. Some other evidence suggests
that Golgi stacks may arise de novo in cells. In the present paper, we review some of the more recent
findings on plant Golgi stack biogenesis and propose a new model for their growth de novo from ER exit
sites.
This document summarizes recent research on the role of chromosome architecture in bacterial cellular organization. It discusses how chromosome structure encodes spatial information that directs processes like chromosome compaction, replication initiation, and segregation. Specifically, it describes how in Caulobacter, the positioning of the origin region near the cell pole facilitates cell cycle regulation. It also explains how the nucleoid provides a scaffold for partitioning systems to segregate chromosomal loci and other cargos through the cell. Finally, it discusses mechanisms in several bacteria by which dynamic changes to chromosome architecture couple replication and segregation to proper placement of the cell division machinery.
This document describes a protocol for engineering cardiac tissue using perfusion bioreactor systems. Cardiac cells are seeded onto porous scaffolds and cultured in bioreactors with perfusion of culture medium, which provides oxygen to the cells and overcomes limitations of conventional static culture. Two approaches are discussed: interstitial flow through porous scaffolds and flow through channel arrays in scaffolds. Perfusion improves cell viability, density, and function compared to static culture and enables engineering of thicker cardiac constructs.
The mating-specific G protein (Gpa1) interacts with the kinesin motor protein Kar3 and regulates pheromone-induced nuclear migration in yeast. Upon pheromone stimulation, Gpa1 polarizes to the incipient growth site early in the mating response, around the same time that microtubules begin attaching to the cortex there. Gpa1 interacts with Kar3 in a microtubule-independent manner upon pheromone stimulation. In the absence of Gpa1, microtubules lose cortical contact upon shrinking and Kar3 is improperly localized, suggesting Gpa1 anchors Kar3 to the cortex. The authors infer that Gpa1 serves as a positional determinant for Kar3-bound microtub
This document summarizes research on interspecies nuclear transfer (iSCNT), where the oocyte and donor cell nucleus come from different species. iSCNT holds promise for overcoming limitations of human oocyte availability for research. Some key points:
- iSCNT has generated human embryonic stem cells and live offspring in closely related animal species. However, success decreases with increasing taxonomic distance between species.
- iSCNT applications include generating human stem cells without human oocytes, and preserving endangered species. Live offspring require complete reprogramming of the donor genome.
- Most iSCNT experiments produce blastocysts, though efficiency varies from 4-44%. Development tends to arrest before embryonic genome activation when
The document discusses sperm development and chromatin structure. It aims to compare methods for evaluating sperm chromatin status in infertile men, specifically image cytometry, computer-assisted semen analysis (CASA), and flow cytometry (FCM). These methods identify spermatogenic cells and evaluate their chromatin structure, which may help assess male factor infertility and predict assisted reproduction outcomes.
This document summarizes a study that investigated the role of ethylene in regulating the trans-differentiation of epidermal cells in Vicia faba (faba bean) cotyledons into transfer cells (TCs) with wall ingrowths. The study found that:
1) Manipulating ethylene biosynthesis and perception affected wall ingrowth formation, indicating ethylene is required to both induce and sustain their development.
2) Ethylene biosynthesis genes were expressed in a spatial and temporal pattern correlated with ethylene production and wall ingrowth induction, preceding their formation.
3) Downstream ethylene signaling components like EIN3 and ERF genes were also differentially expressed
The document discusses the interdependence between the nucleus and cytoplasm in a cell. It provides several examples of experiments that demonstrate how the nucleus controls cytoplasmic activities but also how the cytoplasmic state can influence nuclear behavior and gene expression. Specifically, it notes that enucleated cells can perform some functions but ultimately die without the nucleus, while transferring nuclei between cells shows the nucleus determines traits like cap morphology. The cytoplasmic environment can also reactivate dormant nuclei, as seen when red blood cell nuclei are fused with other cell types. In conclusion, both the nucleus and cytoplasm are necessary as the nucleus directs processes but relies on the cytoplasm as an energy source.
Los profesores Jonathan P. Wojciechowski y Molly M. Stevens, nota realizada en la revista Science, con motivo del artículo publicado por Ivan Sasselli. Revista Science, 374 (6569), • DOI: 10.1126/science.abh3602
4. 2 Intracellular Binding Partners Of Podocalyxin Lab StudyStephanie Roberts
This lab report examines cell motility and the role of cilia. Cilia are hair-like structures on cell surfaces that are important for cell movement and processing external signals during development. Approximately 600 cilia proteins must be synthesized inside cells and transported to cilia through intraflagellar transport. Disruptions to this transport can cause errors in cilia assembly. The report explores different types of cell movement and how the cytoskeleton, composed of microfilaments, microtubules, and intermediate filaments, is the main component enabling motility.
This document summarizes research on sperm cell motility, viability, and calcium regulation. It discusses how sperm motility is regulated by calcium levels, which are controlled by ion channels such as CATsper. Modulating calcium channels and reducing motility may increase sperm cell viability by decreasing reactive oxygen species production. The document also reviews the roles of factors like temperature, membrane potential, and ion currents in modulating calcium concentrations and sperm cell functions like capacitation and the acrosome reaction.
This study examined the similarity of gene expression between sister embryonic stem cells (ESCs) to evaluate the symmetry of cell division. Over 350 pairs of sister ESCs were isolated using microdissection and the expression levels of 48 key genes were analyzed for each cell. The results showed considerable diversity between sister ESCs in normal culture conditions, but significantly higher similarity when cultured in 2i medium, which maintains pluripotency. DNA methyltransferases were downregulated in 2i-grown ESCs, and loss of DNA methyltransferases alone was sufficient to generate nearly identical sister cells, suggesting DNA methylation is a major cause of diversity between sisters and its removal promotes symmetric self-renewal.
This document summarizes a study that examined the effects of culture environment on the mechanical and biochemical properties of cartilage tissue engineered using chondrocytes cultured in agarose gel constructs. The study found that total GAG synthesis was higher in constructs with 4% agarose gel concentration after 7 days of culture. Mechanical testing showed the peak load stress was lower in constructs as the agarose concentration increased. Analysis of the constructs indicated that the total GAG synthesis and mechanical strength of the engineered tissue can be influenced by the agarose concentration and culture time.
This document summarizes a study examining the formation and function of the contractile ring involved in polar body extrusion in the surf clam Spisula. The study found that:
1) The metaphase peripheral aster spreads along the egg cortex in an umbrella-like pattern, leaving a microtubule-poor center.
2) During anaphase, the aster disassembles as a cortical F-actin ring forms that matches the location, size, and pattern of the previous aster.
3) Inhibiting F-actin or myosin blocked polar body formation, while disrupting or stabilizing asters prevented proper ring and polar body formation, supporting the hypothesis that aster spreading
1. Distribution of Callose Synthase, Cellulose Synthase, and
Sucrose Synthase in Tobacco Pollen Tube Is Controlled in
Dissimilar Ways by Actin Filaments and Microtubules1[W]
Giampiero Cai*, Claudia Faleri, Cecilia Del Casino, Anne Mie C. Emons, and Mauro Cresti
`
Dipartimento Scienze Ambientali “G. Sarfatti,” Universita di Siena, 53100 Siena, Italy (G.C., C.F., C.D.C.,
M.C.); Laboratory of Plant Cell Biology, Wageningen University, 6708 PB Wageningen, The Netherlands
(A.M.C.E.); and Department of Biomolecular Systems, Foundation for Fundamental Research on Matter
Institute for Atomic and Molecular Physics, 1098 SJ Amsterdam, The Netherlands (A.M.C.E.)
Callose and cellulose are fundamental components of the cell wall of pollen tubes and are probably synthesized by distinct
enzymes, callose synthase and cellulose synthase, respectively. We examined the distribution of callose synthase and cellulose
synthase in tobacco (Nicotiana tabacum) pollen tubes in relation to the dynamics of actin filaments, microtubules, and the
endomembrane system using specific antibodies to highly conserved peptide sequences. The role of the cytoskeleton and
membrane flow was investigated using specific inhibitors (latrunculin B, 2,3-butanedione monoxime, taxol, oryzalin, and
brefeldin A). Both enzymes are associated with the plasma membrane, but cellulose synthase is present along the entire length
of pollen tubes (with a higher concentration at the apex) while callose synthase is located in the apex and in distal regions. In
longer pollen tubes, callose synthase accumulates consistently around callose plugs, indicating its involvement in plug
synthesis. Actin filaments and endomembrane dynamics are critical for the distribution of callose synthase and cellulose
synthase, showing that enzymes are transported through Golgi bodies and/or vesicles moving along actin filaments.
Conversely, microtubules appear to be critical in the positioning of callose synthase in distal regions and around callose plugs.
In contrast, cellulose synthases are only partially coaligned with cortical microtubules and unrelated to callose plugs. Callose
synthase also comigrates with tubulin by Blue Native-polyacrylamide gel electrophoresis. Membrane sucrose synthase, which
expectedly provides UDP-glucose to callose synthase and cellulose synthase, binds to actin filaments depending on sucrose
concentration; its distribution is dependent on the actin cytoskeleton and the endomembrane system but not on microtubules.
The plant cell wall is composed of cellulose micro- icles is secreted by exocytosis into the existing cell wall
fibrils (CMFs) embedded in the cell wall matrix, a (Miller et al., 1997; Mutwil et al., 2008).
mixture of polysaccharides, glycoproteins, and phe- CMFs are crystalline, parallel b-1,4-glucan chains
nolic substances that interact with each other to that are synthesized at the plasma membrane by the
generate an elaborate three-dimensional structure fun- cellulose synthase complex (CSC), a multiprotein
damental for plant cell development and plant stature. apparatus that presumably consists of 36 individual
The construction of the cell wall in plant cells is a cellulose synthase (CesA) catalytic subunits (Persson
complex process that starts in the endoplasmic retic- et al., 2007; Guerriero et al., 2010). In the intercalary
ulum with the production of enzymes, which are growing cells of the Arabidopsis (Arabidopsis thaliana)
subsequently processed in the Golgi bodies together hypocotyl, CSCs have been observed to be inserted at
with polysaccharides. Enzymes travel by membrane sites of the plasma membrane where Golgi bodies are
trafficking through the Golgi system and end up inside also positioned (Crowell et al., 2009; Gutierrez et al.,
Golgi vesicles and their membrane, which is inserted 2009); furthermore, actin filament (AF)-depolymerizing
into the plasma membrane, while the content of ves- drugs disrupt the distribution of CSCs (Gutierrez
et al., 2009). At the level of individual delivery events,
“small CesA-containing compartments” (Gutierrez
1
This work was supported by the Human Frontier Science et al., 2009) associate with cortical microtubules
Program (project no. RGP0018/2006–C), by the Research Program (MTs; Crowell et al., 2009; Gutierrez et al., 2009) and
of Siena University and Ministry of University and Research 2008 are preferentially delivered to sites where cortical MTs
(Research Projects of National Interest), and by the European Union are present (Gutierrez et al., 2009). The regulation of
Commission (grant no. FP6–2004–NEST–C1–028974 to A.M.C.E.). CesA activity has also been suggested to involve the
* Corresponding author; e-mail cai@unisi.it.
The author responsible for distribution of materials integral to the
internalization of CSCs into membrane compartments
findings presented in this article in accordance with the policy associated with MTs (Crowell et al., 2009). During cell
described in the Instructions for Authors (www.plantphysiol.org) is: wall thickening in local secondary wall formation,
Giampiero Cai (cai@unisi.it). Golgi bodies move along AFs and stop temporarily at
[W]
The online version of this article contains Web-only data. sites where CSCs are to be delivered to the plasma
www.plantphysiol.org/cgi/doi/10.1104/pp.110.171371 membrane, but it is not known if Golgi vesicles move
Plant PhysiologyÒ, March 2011, Vol. 155, pp. 1169–1190, www.plantphysiol.org Ó 2010 American Society of Plant Biologists 1169
2. Cai et al.
along AFs in the final delivery step (Wightman and blotting (Fujii et al., 2010). An association of Sus with
Turner, 2008, 2010). In addition, MTs also direct the CalS has not yet been demonstrated, but some reports
movement of CSCs in the plasma membrane of in- indicate that CalS may be associated (directly or indi-
tercalary elongating cells during the production of rectly) with Sus (Amor et al., 1995; Hong et al., 2001).
CMFs (Paredez et al., 2006; DeBolt et al., 2007a, 2007b; The evidence that pollen tubes have an internal con-
Desprez et al., 2007; Persson et al., 2007; Lloyd and centration of UDPG above the Km of CalS (Schlupmann
Chan, 2008; Lucas and Shaw, 2008; Crowell et al., 2009; et al., 1994) suggests that a membrane-associated Sus
Gutierrez et al., 2009). However, the mode of interac- is not required to deliver the substrate directly to the
tion between MTs and the CSCs is not known. plasma membrane-associated CalS. Nevertheless, Sus
In some plant cells, the cell wall matrix also contains may be required for the maintenance of local higher
callose, a b-1,3-linked Glc polymer with 1,6-branches concentrations of UDPG in order to fuel the molecular
(Chen and Kim 2009). The polymer is synthesized at mechanism that delivers UDPG to CalS. Some authors
many locations during plant development and in (Guerriero et al., 2010) propose that UDPG may be
response to biotic/abiotic stress by callose synthase synthesized by two different mechanisms (one based
(CalS; Verma and Hong, 2001). Interaction of CalS with on UDPG pyrophosphorylase, the other based on Sus),
the cytoskeleton is largely unclear. In the liverwort but no critical proofs are available to validate one or
Riella helicophylla, immunocytological analysis re- the other. The evidence that Sus is an actin-binding
vealed that MTs do not occur at the sites of callose protein led to the proposal that Sus associates with
deposition (Scherp et al., 2002). However, in cells of CalS or CesA at the plasma membrane, thus establish-
Arabidopsis and tobacco (Nicotiana tabacum) treated ing a spatial context for the work of a multiprotein
with oryzalin, the enzyme activity of CalS is signi- complex that facilitates cellulose and callose synthesis
ficantly reduced, suggesting that an intact MT cyto- (Salnikov et al., 2001).
skeleton is required for proper callose synthesis The pollen tube is a cell extension that the pollen
(Aidemark et al., 2009). In BY-2 cells, the correct grain produces upon germination on a receptive
deposition of callose requires proper MT dynamics stigma, and its main function is to carry sperm cells to
because inhibition of MT depolymerization reduced the embryo sac (Higashiyama et al., 2003). The pollen
callose synthesis (Yasuhara, 2005). Interaction between tube elongates by tip growth, a mechanism of cell
AFs and CalS is not known; however, in the secondary expansion confined to the apex, where many secretory
vascular tissues of angiosperms and gymnosperms, vesicles fuse with the plasma membrane (Parton et al.,
myosin, AFs, and callose were observed around the 2001; Ketelaar et al., 2008). Accumulation of Golgi-
pores of sieve elements and sieve cells (Chaffey and derived secretory vesicles in the tube tip is supported
Barlow, 2002). by a polarized actin cytoskeleton, which drives and
Production of cellulose and callose requires UDP- focuses vesicles into the growth region (Geitmann and
Glc (UDPG) that is likely to be provided by cleaving Emons, 2000; for review, see Cole and Fowler, 2006).
Suc molecules, a process carried out by Suc synthase Golgi vesicles, which supposedly contain CesA and
(Sus). Sus is mainly restricted to tissues that metab- CalS in their membranes, are present in the cell tip,
olize Suc (Konishi et al., 2004) and is localized in probably not attached to Golgi bodies (Ketelaar et al.,
different cell structures, such as close to the cytoskel- 2008); vesicles are continuously delivered from the
eton, the tonoplast, and other membranes (Matic et al., basal part of the cell and consumed at the tip during
2004). While a soluble form of Sus is generally in- cell growth. Although vesicle transport could occur by
volved in the cytoplasmic metabolism of Suc, a mem- diffusion, the focusing activity of the actin fringe at the
brane form of Sus is associated with the plasma border of the vesicular area in pollen tubes (Lovy-
membrane or cell wall and has been suggested to Wheeler et al., 2005) and the subapical fine F-actin
provide UDPG for CalS and CesA (Amor et al., 1995). configuration in root hairs (Miller et al., 1999; Ketelaar
A direct association between Sus and CesA is a de- et al., 2003) play roles in vesicle positioning. In pollen
bated question. Although some authors suggest that tubes, AFs polarize the cytoplasm at the tube apex
there is no evidence for direct interactions between (Vidali and Hepler, 2001; Vidali et al., 2001; Lenartow-
CesA and Sus (Guerriero et al., 2010), cooperation ska and Michalska, 2008) and regulate the reversal of
between Sus and CesA is supported by many indirect ´
organelle movement (Cardenas et al., 2005) by pro-
findings. For example, Sus is associated with thicken- gressively extending the cortical actin fringe. The
ings of the secondary cell wall in cotton (Gossypium fringe could also be used as a track to deliver secretory
hirsutum) fibers (Salnikov et al., 2003), and two Sus ´
vesicles to exocytotic sites (Bove et al., 2008; Cardenas
isoenzymes of maize (Zea mays) have a critical role in et al., 2008). On the other hand, the role of MTs in
the synthesis of cellulose (Chourey et al., 1998). In pollen tube growth is still unclear, even though MTs
roots of wheat (Triticum aestivum) under hypoxic con- have been shown to be involved in organelle/vesicle
ditions, the increased enzyme activity of Sus over- transport/localization in vitro (Cai and Cresti, 2009,
lapped the deposition pattern of cellulose (Albrecht 2010).
and Mustroph, 2003). Recently, the catalytic unit of Anisotropic pollen tube development and polariza-
CesA was found to be enriched with a polypeptide tion of membranes and cytoskeleton are also reflected
identified as Sus by mass spectrometry and immuno- in the nonuniform distribution of the cell wall com-
1170 Plant Physiol. Vol. 155, 2011
3. Cellulose, Callose, and Suc Synthase in Pollen Tubes
ponents. The apical region of pollen tubes is charac- cellulose at specific locations and at specific moments
terized by a pectin layer (Li et al., 1995) that extends for during growth. They possess distinct arrays of MTs
the entire tube length and forms the outer cell wall and AFs, which are related to pollen tube growth and
layer. This pectin layer is progressively substituted by along which organelles, including Golgi bodies, move.
a secondary inner layer, mainly consisting of callose We show that CesA and CalS distribute differently in
(around 81%) and cellulose (only 10%; Schlupmann the plasma membrane of tobacco pollen tubes. While
et al., 1994). Although with the use of specific probes, CesA is present mostly in the apical domain and to a
cellulose and callose were not detected in the tube tip lesser extent in the remaining cortical region, CalS is
(Ferguson et al., 1998), electron microscopy after freeze present in the apical domain, in distal regions, and in
fracturing has shown cellulose microfibrils in a direct regions where callose plugs are being formed, consis-
way in this location (Kroh and Knuiman, 1982). Cal- tent with its role in the deposition of these plugs. The
lose is present from 30 mm behind the tip (Ferguson overall distribution of apical CalS, CesA, and Sus is
et al., 1998) and in callose plugs (Cresti and van Went, controlled by AFs, while the distribution of distal CalS
1976; Ferguson et al., 1998). Callose is produced by is primarily controlled by MTs, with which they asso-
CalS, a protein localized in the plasma membrane ciate in Blue Native-PAGE experiments. Membrane
(Ferguson et al., 1998), and activated in vitro by Sus binds to AFs and comigrates with actin in Blue
proteolysis and detergents (Brownfield et al., 2007). Native-PAGE experiments.
CalS in Nicotiana alata pollen tubes consists of a 220-kD
polypeptide, which is likely to be delivered to the
plasma membrane by exocytosis of Golgi membranes RESULTS
(Brownfield et al., 2008). The gene coding for the Antibodies Prepared to CalS Are Specific and Do Not
pollen tube CalS has not yet been identified, but the N. Cross-React with Other Proteins
alata glucan synthase-like 1 (NaGSL1) gene has been
proposed to encode the CalS of N. alata pollen tubes on We raised two antisera against conserved peptides
the basis of several findings. The gene sequence is in the amino acid sequence of CalS from Arabidopsis
highly similar to the fungal 1,3-b-glucan synthase and and N. alata. The antibody DDA was raised against a
is highly expressed in pollen tubes; partially purified peptide sequence located at the C-terminal domain of
CalS contained a 220-kD polypeptide corresponding to CalS and belonging to the glucan synthase domain
the predicted molecular mass of NaGSL1; the protein (Fig. 1A). The antibody HDA was raised against two
was detected by an anti-glucan synthase antibody and peptides at the N terminus of both Nicotiana and
was identified as NaGSL1 using matrix-assisted laser- Arabidopsis CalS that do not belong to the domain of
desorption ionization time of flight mass spectrometry glucan synthase. As expected, the antiserum efficiently
and liquid chromatography-ESI-tandem mass spec- cross-reacted with different quantities of antigenic
trometry analysis of peptides (Brownfield et al., 2007). peptides conjugated to keyhole limpet hemocyanin
The above evidence indicates that NaGSL1 is a strong (KLH; Fig. 1B). As a further control, the secondary
candidate for CalS. Cellulose occurs in lower quanti- antibody alone did not cross-react with the antigenic
ties than callose (Schlupmann et al., 1994). Since it is a peptide (lane Ag+2Ab). Subsequently, HDA was as-
crystalline component, the orientation of cellulose is sayed by immunoblot on cytosolic proteins (Fig. 1C,
potentially important for the architecture of the cell lane 2), membrane proteins (lane 3), and cell wall
wall (Ferguson et al., 1998) and for pollen tube growth proteins (lane 4) from tobacco pollen tubes; extract of
(Anderson et al., 2002). Furthermore, mutation in a mature Arabidopsis flowers (lane 5) was also assayed.
CesA-like sequence of Arabidopsis indicated that the The antibody cross-reacted with a polypeptide of 225
gene product is important for pollen tube growth kD in the protein pool from membrane and cell wall
(Goubet et al., 2003). In the pollen tube, Sus is distrib- fractions of pollen tubes as well as in Arabidopsis
uted at both the plasma membrane and the cell wall, extracts. To validate these results, HDA was affinity
with higher levels detected in the apical and subapical purified by absorption of nitrocellulose membranes
regions. The enzyme activity of Sus is mainly directed coated with peptide antigens (Fig. 1D); the final sam-
to Suc cleavage, and the enzyme exists at least as two ple contained the presumptive heavy and light chains
isoforms that are differently distributed among cell of HDA antibody (lane 4, arrow and arrowhead). The
compartments. The availability of Suc in the germina- antigen unbound antibody fraction (lane 3 of Fig. 1D)
tion medium affects the content and intracellular did not cross-react with cytosolic proteins (Fig. 1E, top
distribution of Sus (Persia et al., 2008), with Sus mostly panel, lane 1), membrane proteins (lane 2), and cell
detected in the plasma membrane and cell wall frac- wall proteins (lane 3) from pollen tubes and against
tions during active growth but found in the cytoplasm Arabidopsis extracts (lane 4). On the contrary, the
during slower growth. This suggests that Suc is a bound/released antibody fraction (lane 4 of Fig. 1D)
general regulator of Sus activity in the pollen tube. efficiently cross-reacted with all samples except for
The pollen tube is an excellent cell type to study the cytoplasmic proteins (Fig. 1E, bottom panel). The
contribution of AFs, MTs, and membrane dynamics in molecular mass and the distribution pattern of the
establishing the correct cellular distribution of CalS, polypeptide recognized by DDA antibody were virtu-
CesA, and Sus. Pollen tubes produce both callose and ally comparable to those recognized by HDA (for the
Plant Physiol. Vol. 155, 2011 1171
4. Cai et al.
Figure 1. Characterization of antibodies to CalS. A, Sequences of CalS used for the production of peptide antibodies. The
antibody DDA was raised against a peptide sequence (in boldface) located at the C-terminal domain of CalS. The antibody
HDA was raised against two peptide sequences (in boldface) found at the N-terminal domain of both N. alata (Na) and
Arabidopsis (At) CalS. In both cases, numbers on the right indicate the positions of sequences in the protein. B, Dot blot
showing the characterization of HDA; the antibody was assayed without antigen (2 Ab) on 1.3, 2.6, 3.9, 5.3, and 6.6 mg of
antigen peptides conjugated to KLH; as a control, the antigen peptide was also tested with the secondary antibody only
(Ag+2Ab). C, Immunoblot showing the screening of HDA antibody on cytosolic proteins from tobacco pollen tubes (lane 2),
membrane proteins (lane 3), and cell wall proteins (lane 4) from tobacco pollen tubes in addition to extract from Arabidopsis
flowers (lane 5); a polypeptide of 225 kD is prominently recognized in lanes 3 to 5. About 30 mg of protein was loaded in each
lane. Prestained Mr markers were loaded in lane 1. All lanes are from the same blot. D, SDS-PAGE showing the partial
purification of HDA antibody by absorption of nitrocellulose membranes coated with antigen peptides. Lane 1, Markers of Mr;
lane 2, starting antiserum; lane 3, unbound proteins; lane 4, absorbed proteins released by acid solution (purified antibody).
Arrow and arrowhead indicate the presumptive heavy and light chains of HDA antibody, respectively. E, Cross-reactivity of
antigen-unbound proteins (sample in lane 3 of D) and of antigen-bound proteins (the purified antibody, lane 4 of D) against
cytosolic proteins (lane 1), membrane proteins (lane 2), and cell wall proteins (lane 3) from pollen tubes and against extracts
of Arabidopsis flowers (lane 4). Lanes contain 30 mg of proteins.
characterization of DDA, see Supplemental Fig. S1), of pollen tubes showed a punctate pattern of labeling
suggesting that the peptide sequences used as antigen (Fig. 2B1); higher magnification images at the apex/
belong to the same or related polypeptide chains. subapex interface showed several spots below the
plasma membrane reminiscent of the distribution of
CalS Localizes Both to the Apical Domain and to Distal vesicles (Fig. 2B2). In longer pollen tubes after 70 min
Regions of Pollen Tubes of growth (about 80 mm in length), staining was again
prominent in the apical domain and in the tube
The HDA antibody was used to determine the restricted to the cortex. In addition, a high density of
intracellular distribution of CalS using immunofluo- CalS was observed in distal segments of the pollen
rescence microscopy. In short pollen tubes after 30 min tube (Fig. 2C, arrow). In longer tubes after 90 min of
of growth (around 40 mm), CalS was mainly detected growth (more than 100 mm), labeling was present in
in the apical domain as a cap in the first 10 mm (Fig. three distinct regions (Fig. 2D): a strong apical stain-
2A, arrow). This region approximately corresponds ing (arrow), an intermediate region characterized by
to the growth area where secretory vesicles and endo- slighter staining (arrowhead), and a distal segment in
cytotic vesicles are observed with the electron mi- which labeling was stronger again (bordered arrow).
croscope. This domain was followed by a less intense The length of segments occupied by each location was
labeling area, which covered the remaining tube quantified in 3-h-grown pollen tubes by measuring the
length (Fig. 2A, arrowhead). When observed at focal fluorescence intensity along the shank of pollen tubes,
planes tangential to the tube cortex, the apical region from the tip down to the base region (Fig. 2E). Values
1172 Plant Physiol. Vol. 155, 2011
5. Cellulose, Callose, and Suc Synthase in Pollen Tubes
Figure 2. Distribution of CalS as shown by HDA antibody in immunofluorescence microscopy. Images in A, C, and D are single
focal planes obtained in the tube center, while images in B and F are focused at the tube cortex. A, In short pollen tubes, labeling
of CalS was mainly found in the cortical region of the apical domain (arrow); labeling extended approximately for the first 20 mm.
This region was followed by less intense labeling, which was located in the cortex of pollen tubes and extended toward the
pollen grain (arrowhead). B, Magnification of the apical region of pollen tubes showing the dotted distribution pattern of CalS.
B1, Image of a single focal plane tangential at the tube surface. B2, Magnification of a focal plane in the tube center highlighting
the presence of fluorescent spots in proximity of the tube apex (arrows). C, In longer pollen tubes, the slightly fluorescent region
was followed by a distal region in which fluorescence intensity increased (arrow). D, In even longer tubes, the three-patterned
distribution of CalS is more evident: the apical stronger region (arrow), the intermediate slighter region (arrowhead), and the
distal intense region (bordered arrow); in all cases, staining is mainly cortical. E, Measurement of fluorescence intensity along the
shank of pollen tubes, from the tip down to the base region. The three-segmented distribution of CalS is evident. F and G, In
double labeling experiments performed on untreated pollen tubes, CalS (red, arrows) was sometimes found to colocalize with
microtubules (green). Bars = 10 mm (A, B1, C, and D), 3 mm (B2), and 5 mm (F and G). H, Distribution of CalS in pollen tubes after
plasmolysis. H1, Most of the CalS signal is found in the collapsing cytoplasm (arrow), and only a faint signal is found in the cell
wall (arrowhead). H2, Corresponding DIC image. Bar = 10 mm.
are averages of data collected on different pollen tubes therefore is not included in the graph. When pollen
(at least 20 pollen tubes) with equivalent length. The tubes were stained for CalS and tubulin, we often
fluorescence profile shows that CalS is distinctly dis- found colocalization of CalS spots (red) with MTs
tributed in the initial 15 to 20 mm of the pollen tube (green) in distal regions, corresponding to the third
and, after a lower intensity segment of 40 to 60 mm, it segment of labeling where the presence of CalS is more
reappears at higher abundance around 100 mm from abundant (Fig. 2, F and G, arrows). To quantify the
the tube tip. Autofluorescence in control pollen tubes colocalization between CalS and MTs, we analyzed
(without primary antibody) was practically absent and several double immunofluorescence images (n = 10;
Plant Physiol. Vol. 155, 2011 1173
6. Cai et al.
single focal planes) for the following correlation coef- (DIC) microscopy (Fig. 3A, arrow). When the same plug
ficients using the JACoP plugin for ImageJ (http://rsb. was observed after anti-CalS labeling (Fig. 3B), we
info.nih.gov/ij/plugins/track/jacop.html). The Pear- noted a considerable increase of CalS on both sides of
son correlation coefficient was 0.63; the Manders the callose plug; labeling was lost in the older mature
(overlap) coefficient was 0.84 with M1 (fraction of (central) region of the plug (asterisk). On the side of the
CalS overlapping MTs) corresponding to 0.81 and M2 developing plug, CalS was distributed as dots, appar-
(fraction of MTs overlapping CalS) equivalent to 0.24; ently aligned along the border of the callose plug (Fig.
the Van Steensel cross-correlation coefficient showed a 3B, arrows). In most of the pollen tubes, the region
bell-shaped curve peaking to one side. All these coef- around plugs (Fig. 3C, arrow) was strongly labeled by
ficients indicate a consistent (although not complete) anti-CalS, revealing a consistent accumulation of CalS
colocalization between CalS dots and cortical MTs. around the callose plug (Fig. 3D, in red). In the same
Association of CalS with the plasma membrane of samples, MTs were observed to pass through the plug
pollen tubes was also shown by plasmolysis (Fig. 2, H1 hole longitudinally, mixed with several CalS dots (Fig.
and H2); after plasmolysis, most of the CalS signal was 3D, in green). Colocalization of CalS and MTs around
retained in the collapsing cytoplasm (arrow), while a the callose plug is suggested at higher magnification in
faint signal remained in the cell wall (arrowhead). double labeling experiments. CalS dots (Fig. 3E, in red,
In longer pollen tubes (more than 9 h of growth, arrows) appeared as aligned along cortical MTs (in
around 900 mm long), four to five callose plugs had green) on the side of the growing plug. The Pearson
been formed, with the first callose plug forming after coefficient was 0.70, while the Manders coefficients
4 h of growth, around 300 mm of pollen tube length were M1 = 0.71 (fraction of CalS overlapping MTs) and
(for statistical evaluation of callose plug formation, see M2 = 0.29 (fraction of MTs overlapping CalS); in addi-
Laitiainen et al., 2002). We found that CalS accumulated tion, the Van Steensel cross-correlation coefficient again
during the development of callose plugs, which were showed a bell-shaped curve peaking on one side. We
easily observable using differential interference contrast also analyzed the distribution of Sus in and around the
Figure 3. Localization of CalS in the callose plugs of pollen tubes. Longer pollen tubes (about 9 h of growth) were labeled by
anti-CalS in order to analyze the distribution of CalS in comparison with callose plugs. A, A developing callose plug, which was
observable using DIC microscopy (arrow). B, The same plug observed after immunostaining with anti-CalS showed a substantial
increase of CalS on both sides, but labeling was absent on the central mature region of the plug (asterisk). On the side of the
growing plug, CalS appeared as dots aligned along the border of the callose plug (arrows). Bars = 10 mm. C and D, One pollen
tube with a developing callose plug (C, arrow) also showed a strong labeling by anti-CalS antibody around the plug (D; in red);
MTs appeared as strands still passing through the narrow hole formed by the plug (D; in green). Bars = 10 mm. E, At higher
magnification, CalS (in red) appeared as dots (arrows) aligned on cortical MTs (in green) on the side of the growing callose plug
(CP). Bar = 5 mm. F and G, Analysis of Sus distribution at the level of callose plugs. When a callose plug formed (indicated by the
arrow in the DIC image in F), the relative amount of Sus in its proximity increased significantly and prominent accumulation of
Sus on both sides of the callose plugs was observed (G; arrowheads). Bar = 20 mm.
1174 Plant Physiol. Vol. 155, 2011
7. Cellulose, Callose, and Suc Synthase in Pollen Tubes
callose plugs. Most of the membrane Sus in tobacco level of the subapex showed gold particles in close
pollen tubes was associated with the cortical region association with vesicle-like structures (Fig. 4B), sug-
(plasma membrane and cell wall), with a considerably gesting that CalS is transported to the plasma mem-
higher concentration in the proximity of callose plugs brane inside the membrane of vesicles. The putative
(arrow in the DIC image in Fig. 3F). We regularly association of gold particles with the plasma membrane
observed an accumulation of Sus on both sides of the is more evident in magnified images (Fig. 4C, arrows).
callose plugs (Fig. 3G, arrowheads). In the region next to the subapex, only a few gold
Quantitative information on the distribution of CalS particles could be detected (57 6 13 gold particles
in pollen tubes was obtained by immunogold electron mm22), in accordance with results of immunofluores-
microscopy. We analyzed different regions of tobacco cence microscopy. In such cases, the percentage of gold
pollen tubes, the positions of which are approximately particles in the cell wall region matched that found in
indicated by the drawing on the right side of Figure 4. the cytoplasm (Fig. 4D). In more distal regions, the
The apical region of pollen tubes (Fig. 4A) was charac- number of gold particles increased considerably (496 6
terized by a large number of gold particles (563 6 47 41 gold particles mm22), and they still maintained their
gold particles mm22), which were mostly concentrated association with the plasma membrane and cell wall
at the interface between the plasma membrane and the (Fig. 4E). This is the region where the first callose plug is
cell wall. A limited number of gold particles were also expected to be formed (Cheung, 1996; Laitiainen et al.,
found in the pollen tube cytoplasm (25 6 11 gold 2002). Again, gold particles in the cell wall region
particles mm22), whereas very few (most likely nonspe- accounted for more than 85% 6 5% of total particles.
cific) particles were found outside of the pollen tube. When observed at higher magnification, gold parti-
When particles were counted using the ImageJ soft- cles in the distal region were found to line up con-
ware, the cell wall region (probably comprising the sistently at the interface between cytoplasm and cell
plasma membrane) accounted for more than 80% 6 5% wall, presumably the plasma membrane (Fig. 4F,
of gold particles in each electron micrograph, while arrows). If the cell wall surface was arbitrarily di-
the pollen tube cytoplasm contained 20% 6 3% and vided into three consecutive regions (one closer to the
the outside of pollen tubes (i.e. the inclusion resin) ac- plasma membrane, one intermediate, and the last in
counted for only 1% 6 0.5% of particles. Images at the touch with the inclusion resin), more than 90% of gold
Figure 4. Immunogold electron microscopy of CalS in pollen tubes. The drawing on the right indicates the approximate
position of the electron micrographs and the density of gold particles (gp) mm22 in each sample. A, View of the apical region
of pollen tubes. A large number of gold particles can be observed; most of them are concentrated at the plasma membrane/
cell wall (CW) interface. Bar = 350 nm. B, Labeling of CalS in the apical region, suggesting an association with vesicle-like
structures. Bar = 150 nm. C, Magnification of labeling in the apical domain showing the presumptive association of gold
particles with the plasma membrane (arrows). Bar = 250 nm. D, View of CalS distribution in the intermediate region. Few gold
particles can be detected. Bar = 350 nm. E, View of distal regions of pollen tubes. The number of gold particles at the plasma
membrane/cell wall interface increased considerably. Bar = 350 nm. F, When observed at higher magnification, gold particles
in the distal region were lined up at the plasma membrane/cell wall interface (arrows), suggesting an association with the
plasma membrane. Bar = 250 nm.
Plant Physiol. Vol. 155, 2011 1175
8. Cai et al.
particles were found in the first cell wall segment. We that staining was found in the cortical region of pollen
think that the electron micrographs showed undoubt- tubes, with the exception of the apical domain, where
edly the membrane localization of CalS; because of its labeling was also detected in the cytoplasm (asterisk),
size, the label of the antibody sticks out from the anti- probably in association with Golgi-derived vesicles.
genic size at the electron microscopy resolution and When the relative fluorescence intensity of CesA was
could be responsible for the labeling in the pollen tube measured along the tube border, the resulting graph
cell wall. confirmed a higher intensity of staining in the apical
Distance between the different regions of Figure 4 domain and a progressive decrease to constant levels at
was difficult to calculate, because pollen tubes were 40 to 50 mm from the tube apex (Fig. 5C). Compared
first embedded in a resin block, which was cut into with CalS staining, no additional labeled areas were
smaller pieces before finely cutting on a ultramicro- found in distal segments of pollen tubes. The dotted
tome. On the basis of the “precut” (necessary to select nature of labeling was revealed by the high number of
specific regions), we can only affirm that Figure 4D is graph peaks and by distinct fluorescence dots observed
about 40 to 50 mm and that Figure 4E is around 90 to in tangential focal planes (Fig. 5D). Measurement of the
100 mm from the pollen tube apex. distance between spots in tangential focal planes (such
as the one shown in Fig. 5D2) returned an average
CesA Is Present All through the Pollen Tube Cortex distance between adjacent spots of 0.78 6 0.22 mm (n =
100). The density of fluorescent spots was 1.53 6 0.14
In order to monitor the distribution of CesA, we took per mm2 (n = 50). In tangential focal planes at the level
advantage of an antiserum (generously provided by of the plasma membrane/cell wall (Fig. 5D1), CesA
Prof. Chris Somerville) that cross-reacted with a con- particles were abundantly present; sometimes, they
served peptide sequence present in all CesA molecules aligned along invisible tracks (arrow), which might
(Gillmor et al., 2002). When tested on different protein represent underlying MTs. In the same sample, with the
extracts, the antiserum cross-reacted with a 125-kD focal plane just below the plasma membrane (0.3 mm
polypeptide in the Arabidopsis extracts (Fig. 5A, lane from the previous one; Fig. 5D2), in the area where
1), in the membrane protein fraction (lane 3), in the vesicles are present, CesA was localized in that region
Triton-extracted cell wall proteins (lane 4), and weakly also in particles but with different alignment compared
in the NaCl-extracted cell wall proteins (lane 5) from with the previous focal plane. At focal planes in the
tobacco pollen tubes. The cross-reacting polypeptide middle of the same pollen tube (Fig. 5D3), CesA was
was detected neither in the cytoplasmic protein pool found only in the cortex. We also tested by double im-
(lane 2) nor in the SDS-solubilized protein fraction from munofluorescence microscopy the putative coalign-
the cell wall (lane 6). Background noise was noticeable ment of CesA particles with MTs in the cortex of
in all lanes, but reaction was specific. We have not pollen tubes (Fig. 5, E and F). Although some CesA
purified CesA; therefore, we did not test the reactivity particles (red) occasionally aligned with MTs (green),
of the anti-CalS antibody on purified CesA. In immu- we never found a precise codistribution between MTs
noblots, the anti-CesA and anti-CalS antibodies cross- and CesA proteins. The Pearson coefficient was only
reacted with proteins of different molecular mass (125 0.32, while the Manders coefficients were M1 = 0.18
kD for CesA versus 225 kD for CalS). Although the (fraction of CesA overlapping MTs) and M2 = 0.264
immunolocalization pattern of the two proteins was (fraction of MTs overlapping CesA); furthermore, the
occasionally similar in the pollen tube, the inhibitory Van Steensel cross-correlation coefficient returned a
experiments (see below) suggest that the two antigens three-peaked curve with only one peaking in the center.
belong definitely to different proteins. In addition, CesA particles were dispersed among MTs as well as
when the anti-CalS antibody was preabsorbed on the positioned along MT bundles, suggesting that their
antigenic peptide, no signal was observed in immuno- relationship (if present) does not consist of precise
blots at the level of the CesA molecular mass. Evidence coalignment. However, an in vivo study is required to
of CesA in the NaCl cell wall fraction raised the make definitive statements here.
question of whether CesA in the cell wall is a contam- The distribution of CesA in the apical and subapi-
ination in the procedure. We think that the presence of cal regions of pollen tubes was also investigated by
CesA in the pollen tube cell wall is dependent on the immunogold labeling. CesA was mainly observed in
extraction procedure, which probably leaves some association with the cortical region of tobacco pollen
plasma membrane remnants in association with the tubes, presumably with the plasma membrane (Fig.
cell wall; in confirmation of this hypothesis, CesA could 5G, arrows). Gold particles were also found in associ-
be easily removed by NaCl treatment. ation with vesicular structures just below the plasma
The distribution of CesA proteins was different com- membrane (Fig. 5G, arrowheads) and with Golgi
pared with CalS. When used in immunofluorescence bodies (bordered arrow). In general, the association
microscopy, the CesA antiserum depicted a punctate of gold particles with the plasma membrane (Fig. 5H,
pattern at the cell border, which was more evident in arrow) and with vesicular structures of approximately
the apical domain (Fig. 5B, arrow) and progressively 100 to 150 nm close to the plasma membrane (Fig. 5, I
weaker in the remaining part of pollen tubes (arrow- and J, asterisks) was the most prominent feature of
head). Focal sections fixed at the tube center revealed CesA distribution.
1176 Plant Physiol. Vol. 155, 2011
9. Cellulose, Callose, and Suc Synthase in Pollen Tubes
Figure 5. Characterization of CesA in tobacco pollen tubes. A, Immunoblot with anti-CesA antibody on Arabidopsis extract (20 mg;
lane 1), cytosolic proteins (20 mg; lane 2), membrane proteins (20 mg; lane 3), Triton-solubilized cell wall proteins (10 mg; lane 4),
NaCl-solubilized cell wall proteins (10 mg; lane 5), and SDS-solubilized cell wall proteins (5 mg; lane 6) from tobacco pollen tubes.
The arrowhead indicates the main cross-reacting band around 125 kD in the Arabidopsis, membrane, Triton-, and NaCl-extracted
proteins. B, Immunolocalization of CesA in tobacco pollen tubes. The image was captured in the center of the pollen tube. Staining
was mainly observed in the apical domain (arrow) and to a lesser extent in the remaining cortical region (arrowhead). In the apex,
staining was also diffusely observed in the cytoplasmic domain (asterisk), presumably in association with vesicular material. C,
Measure of fluorescence intensity along the cell border of pollen tubes emphasizing the higher signal in the apex and the progressive
decline toward a basal level. The presence of numerous peaks indicates the spot-like distribution of CesA proteins. D, A single pollen
tube observed at three different focal planes: D1, tangential to the surface (presumably plasma membrane and cell wall); D2, just
below the plasma membrane; D3, in the middle. CesA was distributed differently. The arrow indicates invisible tracks along which
CesA spots align. Bar = 10 mm. E and F, Double immunolocalization of microtubules (green) and CesA (red). CesA proteins appeared
as dots sometimes coaligning with microtubules but also distributed between microtubule bundles. Bars = 5 mm. G, Immunogold
labeling of CesA. The protein was detected in association with the plasma membrane (arrows), with vesicular structures below the
plasmalemma (arrowheads) and with Golgi bodies (bordered arrow). Bar = 250 nm. H to J, Immunogold labeling of CesA in
the cortex of pollen tubes. CesA was mainly found in association with the cortical region of tobacco pollen tubes, presumably with
the plasma membrane (H; arrow). Gold particles were frequently found in association with vesicular structures (asterisks) of around
100 to 150 nm that accumulate in proximity of the plasma membrane (I and J). Bars = 250 nm.
Biochemical Fractionation of Pollen Tube Membranes plasma membrane. In order to determine the subcel-
Shows that CalS, CesA, and Sus Are Associated with the lular membrane compartment associated with CesA
Plasma Membrane and CalS, we separated the membrane pool of 9- to 12-
Immunofluorescence and electron micrographs h-grown pollen tubes into 20 fractions by centrifuga-
show that CesA and CalS are associated with the tion along 8% to 65% continuous Suc gradients. In the
cortical region of pollen tubes, expectedly with the SDS-PAGE of Figure 6A, only 17 out of 20 fractions are
Plant Physiol. Vol. 155, 2011 1177
10. Cai et al.
shown, with fraction 1 corresponding to 8% and frac- Binding of Membrane Sus to Actin Filaments
tion 17 corresponding to 57% Suc. Fractions were Requires Suc
assayed by immunoblot with anti-CesA antibody,
which revealed the 125-kD band mainly in fractions Since Sus has been suggested to be an actin-binding
8 to 13 (Fig. 6B). CalS, visualized by immunoblot with protein (Winter et al., 1998), we analyzed the binding
HDA (Fig. 6C), and Sus, which was labeled by K2 affinity between pollen Sus and AFs and its depen-
antibody (Heinlein and Starlinger, 1989; Fig. 6D), dence on Suc concentration. At first, cytoplasmic Sus
sedimented approximately in the same fractions. A of pollen tubes was assayed for its affinity to AFs (Fig.
minor secondary peak of Sus was also found in frac- 7A). After mixing cytosolic proteins of pollen tubes
tions 4 and 5. As a control, the positions of both tubulin (lane 2) with AFs (lane 3) in the absence (lanes 8 and
and actin were also tested using specific antibodies. 9) and in the presence of either 40 mM Suc (lanes
Tubulin was found to distribute as a broader peak with 10 and 11) or 100 mM Suc (lanes 12 and 13), the
a maximum in fraction 10, thus comparably to CesA, distribution of Sus was analyzed by immunoblot with
CalS, and Sus; on the other hand, actin distributed in anti-Sus antibody (Fig. 7B). As a result, cytoplasmic
all fractions, indicating that actin associates with a Sus bound to AFs in the absence of Suc (pellet of lane
variety of intracellular membranes. Further confirma- 9) but not in the presence of either 40 or 100 mM Suc
tion of codistribution among CesA, CalS, and Sus was (pellets of lane 11 and 13). When AFs were omitted,
obtained by measuring their immunoblot profiles cytosolic proteins (Fig. 7A, lane 6) and Sus (Fig. 7B,
from three independent immunoblots and averaging lane 6) were found in the supernatant. In control
their values; results show that CalS, CesA, and Sus samples, bovine serum albumin (BSA) was assayed
peak around fraction 10 (Supplemental Fig. S2). When for its binding capacity to AFs in either the absence
enzyme markers for different membrane compart- of Suc (Fig. 7A, lanes 12 and 13) or in the presence
ments were analyzed, fraction 10 was found to be of 40 and 100 mM Suc; in all cases, BSA was consis-
enriched in the plasma membrane marker P-ATPase, tently found in the supernatant. Actin filaments alone
with other organelle markers sedimenting in different were almost exclusively detected in the pellet (Fig.
fractions (bottom part of Fig. 6). 7A, lane 5).
Figure 6. Suc density gradient fractionation of
pollen tube membranes. A, The microsomal
fraction from 9-h-grown tobacco pollen tubes
was centrifuged along 8% to 65% continuous
Suc gradients and separated into approxi-
mately 20 fractions. Only 17 out of 20 frac-
tions are shown on the SDS-PAGE gel (fraction
1 corresponds to 8% Suc, and fraction 17
corresponds roughly to 57% Suc). Molecular
mass markers in kD (M) are on the left.
Equivalent volumes were loaded. B, Immuno-
blot with anti-CesA antibody on the same
fractions. The 125-kD band is found in frac-
tions 8 to 13. C, Immunoblot with HDA
antibody, which detected CalS in fractions 8
to 12. D, Immunoblot with K2 antibody
against Sus; the enzyme peaked around frac-
tions 8 to 12, while a small secondary peak
was found in fractions 4 and 5. E, Immunoblot
with anti-tubulin antibody showing the distri-
bution of pollen tubulin. F, Immunoblot with
anti-actin antibody. The positions of enzyme
markers specific for different cellular com-
partments are also indicated: inosine-5#-di-
phosphate (IDPase) for Golgi membranes,
cytochrome c reductase (CCR) for endoplas-
mic reticulum, P-ATPase for plasma mem-
brane, and cytochrome c oxidase (CCO) for
mitochondria.
1178 Plant Physiol. Vol. 155, 2011
11. Cellulose, Callose, and Suc Synthase in Pollen Tubes
The behavior of membrane Sus was different (Fig.
7C). Triton-extracted proteins of pollen tubes (lane 4)
were mixed with AFs (lane 2) and incubated in the
absence of Suc (lanes 7 and 8) and in the presence of
either 40 mM Suc (lanes 9 and 10) or 100 mM Suc (lanes
11 and 12). After centrifugation, immunoblots with
anti-Sus (Fig. 7D) showed the presence of membrane
Sus in the Triton-extracted protein fraction (lane 4) and
consistently in the actin pellets obtained in the pres-
ence of either 40 mM Suc (lane 10) or 100 mM Suc (lane
12). On the contrary, membrane Sus did not sediment
(or poorly) with AFs in the absence of Suc (lane 8). As
expected, Sus did not sediment in the absence of AFs
(Fig. 7D, lane 6). These data indicate that the rise of Suc
concentration abolished the binding of cytoplasmic
Sus to AFs while increasing progressively the affinity
of membrane Sus to AFs and suggest that the avail-
ability of Suc affects the distribution of Sus. Again, in
control samples, BSA was unable to bind to AFs in
either the absence (Fig. 7C, lanes 13 and 14) or the
presence of 40 and 100 mM Suc.
On the other hand, Sus did not bind to MTs and the
binding was not affected by Suc concentration (Fig. 8,
A and B). Cytosolic proteins did not pellet in the
absence of MTs (Fig. 8A, lanes 4 and 5), while tubulin
prominently sedimented (lanes 6 and 7). When mixed
with MTs, part of the cytosolic proteins bound to
MTs and sedimented (lanes 8 and 9), but Sus was still
found in the supernatant (Fig. 8B, blot of lanes 8 and
9). Addition of Suc to the mix did not allow Sus to
associate with MTs and to sediment (Fig. 8A, 40 mM
Suc in lanes 10 and 11, 100 mM Suc in lanes 12 and 13).
The behavior of Sus was similar to that of BSA, used as
a control for non-MT-binding protein (lanes 14 and 15).
Like cytoplasmic Sus, membrane Sus did not bind to
MTs under any Suc concentration (the result is prac-
tically equivalent to cytoplasmic Sus and therefore is
not shown).
To test further the putative interaction between
cytoskeleton components (AFs and MTs) and the
studied enzymes (Sus, CalS, and CesA), Blue Native-
PAGE was used to separate native protein complexes
of the plasma membrane of tobacco pollen tubes (Fig.
8C). After separation in the first dimension according
to the native molecular mass and in the second di-
Figure 7.Binding assay of Sus to actin filaments. A, Binding of cyto-
plasmic Sus. Lane 1, Molecular mass markers; lane 2, cytosolic proteins membrane Sus. Lane 1, Molecular mass markers. Triton-extracted
of pollen tubes (20 mg); lane 3, actin filaments (5 mg). When samples proteins (lane 4; 20 mg) were mixed with actin filaments (lane 2; 5 mg)
were incubated and centrifuged (S, supernatant; P, pellet), F-actin alone and centrifuged (S, supernatant; P, pellet). When actin filaments were
was essentially found in the pellet (lane 5) in comparison with the omitted, membrane proteins did not sediment (lane 6). Membrane
supernatant (lane 4). Conversely, cytosolic proteins alone were found in proteins were incubated with actin filaments in the absence of Suc
the supernatant (lane 6) but not in the pellet (lane 7). Cytosolic proteins (lanes 7 and 8) and in the presence of either 40 mM Suc (lanes 9 and 10)
were mixed with actin in the absence (lanes 8 and 9) or in the presence or 100 mM Suc (lanes 11 and 12). As a control, BSA was also mixed with
of 40 mM Suc (lanes 10 and 11) or 100 mM Suc (lanes 12 and 13). As a actin (lanes 13 and 14). D, Immunoblot with anti-Sus on the fractions
control, BSA was also mixed with actin filaments (lanes 14 and 15). B, shown in C. Sus was found in the Triton-extracted protein fraction (lane
Immunoblot with anti-Sus on some of the fraction shown in A. Sus was 4), but it did not sediment in the absence of actin (lane 6). Sus did not
found in the unsedimented cytosolic proteins (lane 6) and in associ- sediment as well in the absence of Suc (lane 8), but it pelleted with actin
ation with actin filaments in the absence of Suc (lane 9) but not in the in the presence of either 40 mM Suc (lane 10) or 100 mM Suc (lane 12).
presence of either 40 or 100 mM Suc (lanes 11 and 13). C, Binding of Blots in D are from the same nitrocellulose membrane.
Plant Physiol. Vol. 155, 2011 1179
12. Cai et al.
mension by standard SDS-PAGE, CalS appeared in a
protein complex with an approximate mass of 1,600
kD (Fig. 8D, CalS). Tubulin apparently comigrated
with CalS in the high molecular mass complex through
a physical interaction sufficiently strong to remain
during protein isolation. On the other hand, Sus was
found to migrate in a protein complex with a mass of
around 500 kD (Sus), which also contained actin. Immu-
noreactivity of Sus was also found in spots around
140 kD (possibly a dimer) and, more interestingly, in
higher molecular mass complexes comigrating with
CalS and tubulin. These data indicate that Sus can be
found at various locations in the pollen tube plasma
membrane, mainly in association with actin but also
probably with CalS; however, actin did not bind to
CalS. Unfortunately, CesA was not detected by immu-
noblot; consequently, it was not possible to establish its
association with other proteins.
Inhibitors of Cytoskeleton and Membrane Dynamics
Affect Differently the Distribution of CalS, CesA, and
Sus in the Pollen Tube
The aim of this work was to determine the distribu-
tion of CalS, CesA, and Sus in relation to cytoskeleton
dynamics and endomembrane trafficking. In order to
monitor the distribution of vesicles in the tube apex
during inhibitory experiments, we took advantage of
tobacco plants expressing GFP-labeled Rab11b, a
GTPase present in vesicles (de Graaf et al., 2005). The
distribution of CalS, CesA, and Sus and the endomem-
brane trafficking were analyzed using the drug bre-
feldin A (BFA), which affects membrane trafficking
via release/inactivation of Golgi body coat proteins
¨
(Nebenfuhr et al., 2002). The consequences of MT
depolymerization and stabilization were analyzed us-
ing oryzalin and taxol, respectively (Astro ¨m, 1992;
Astrom et al., 1995; Gossot and Geitmann, 2007). The
role of myosin was investigated using the inhibitor 2,3-
butanedione monoxime (BDM), which is known to
block myosin activity (Tominaga et al., 2000), while the
effect of AF depolymerization was analyzed using
´
latrunculin B (LatB; Cardenas et al., 2008).
In untreated pollen tubes, GFP:Rab11b-containing
vesicles were mainly present in the tube apex in the
typical inverted cone shape; Golgi bodies with vesicles
Figure 8. Binding of cytoplasmic Sus to microtubules and analysis of move toward the tip in the pollen tube cortex and turn
CalS complex by Blue Native-PAGE. A, SDS-PAGE of the binding assay back in the tube center, leaving the vesicles in the apex.
of Sus to microtubules. For clarity, the content of lanes is explained
BFA induced an accumulation of membranes in the
together with information for B. S, Supernatant; P, pellet. B, Immu-
noblot with anti-Sus on some of the fractions shown in A. Lane 1,
subapical region, generating the so-called BFA mem-
Molecular mass markers. Cytosolic proteins (lane 2; 20 mg) assayed in
the absence of microtubules (lane 3; 7 mg) did not sediment (lanes 4
and 5). When microtubules were added in the absence of Suc (lanes 8 separated according to their native molecular mass along 4% to 12%
and 9), part of cytosolic proteins bound to MTs and sedimented but Sus gels (horizontal axis) and then by standard SDS-PAGE on 10% gels
was still found in the supernatant (B, lanes 8 and 9). The presence of Suc (vertical axis). Standards of native molecular mass are indicated on top,
in the mix did not allow Sus to sediment with MTs (40 mM Suc in lanes while SDS-PAGE standards are indicated on the left. D, Immunoblot
10 and 11, 100 mM Suc in lanes 12 and 13). The behavior of Sus was with antibodies to CalS, tubulin, Sus, and actin showing their relative
similar to that of the control protein BSA (lanes 14 and 15). Lanes 6 to 7, migration after Blue Native (BN)-PAGE. Tubulin and CalS cosedimented
Control of microtubule sedimentation activity. All lanes in A are from in a higher molecular mass region around 1,600 kD, while Sus and
the same gel. C, Blue Native-PAGE of plasma membrane proteins actin cosedimented around 500 kD.
1180 Plant Physiol. Vol. 155, 2011
13. Cellulose, Callose, and Suc Synthase in Pollen Tubes
brane compartment (Fig. 9A, arrow in BFA panel). more consistently after treatment with either taxol or
LatB caused a progressive dispersion of the GFP: oryzalin. Interestingly, the two accumulation areas do
Rab11b-containing vesicles and thus disappearance not overlap: the BFA-dependent accumulation in-
of the inverted cone. Inhibition of myosin activity by creased markedly in the region 80 to 90 mm behind
BDM caused a progressive stop of organelle move- the apex and then dropped down; by contrast, the
ment and a uniform dispersion of the GFP:Rab11b- taxol/oryzalin-dependent accumulation was found
containing vesicles along the pollen tube, confirming around 100 to 120 mm behind the apex, where the first
that myosin activity is critical for focusing vesicles in callose plug is expected to be formed.
the pollen tube apex. Oryzalin and taxol caused only Treatment with inhibitors had different effects on the
slightly perceptible effects on the distribution of the distribution of CesA proteins (Fig. 9C). In comparison
GFP:Rab11b-containing vesicles. Oryzalin generated a with controls (Fig. 5B), a clear change in CesA distri-
more rounded shape of the vesicular cone, while taxol bution was revealed after treatment with BFA: the drug
caused the tail of the vesicle cone to extend farther caused a progressive and consistent intracellular accu-
from the cell tip. mulation of CesA in the cytoplasm of distal regions
In comparison with controls (Fig. 2), BFA induced (arrow) and a concomitant decrease of CesA in the
a progressive accumulation of intracellular deposits apical region (asterisk). This change is more evident in
of CalS in distal regions (Fig. 9B, arrowhead in BFA time-course experiments (Supplemental Fig. S5A) and
panel), showing that the enzyme is located in the shows that CesA travels through the endomembrane
endomembrane system. The apical accumulation of system. Treatment with LatB caused the disorganiza-
CalS was maintained to a lesser extent (for a time- tion of AFs in the apical and subapical regions of pollen
course experiment, see Supplemental Fig. S3A). LatB tubes (Fig. 9E); consequently, the drug induced a pro-
affected the apical distribution of CalS already con- gressive redistribution of CesA. Unlike the effect on
siderably after 15 min (Fig. 9B, LatB top panel) and CalS, LatB produced a progressive relocation of
more pronouncedly after 30 min (bottom panel), with CesA rather than a disappearance (Supplemental
CalS appearing in the rest of the cytoplasm (for a time Fig. S5B). When the myosin inhibitor BDM was used,
course experiment, see Supplemental Fig. S3B). Both CesA persisted in the apical/subapical regions but
changes are expected, since we showed that the en- fluorescence intensity was lower (for a time-course
zyme is in the endomembrane system. Inhibition of experiment, see Supplemental Fig. S5C). The MT-
myosin activity by BDM treatment caused CalS to depolymerizing drug oryzalin, at a concentration
accumulate to a lesser extent in the apical domain and that caused complete depolymerization of MTs (Fig.
to disappear progressively from distal regions of pol- 9F), caused no significant changes in the distribution
len tubes, leading to the loss of the three-patterned of CesA, and the enzyme appeared again more
organization. After a 30-min treatment (Supplemen- concentrated in the apex/subapex. Taxol treatment
tal Fig. S3C), the apical cortical distribution of CalS showed no significant effects as well: the pattern of
changed into a dispersed intracellular organization. CesA proteins was relatively comparable to controls,
Therefore, the actin-myosin activity influences the suggesting again that MTs were not critical for CesA
transport and accumulation of CalS. Oryzalin and distribution (for time-course experiments, see Sup-
taxol had more specific effects: in the presence of plemental Fig. S5, D and E). When the fluorescence
oryzalin, the apical distribution of CalS was relatively intensity of CesA after oryzalin and LatB treatment
unaffected but the organization of CalS in distal was measured, results confirmed that the distribu-
regions was dramatically disturbed, with the appear- tion of CesA was unaffected by oryzalin (Supple-
ance of consistent intracellular deposits (asterisk in mental Fig. S6A); although the signal in the apical
the time course experiment of Supplemental Fig. dome was weaker than the control, the slope of
S3D). Taxol showed comparable effects: the apical intensity was unchanged. On the other hand, treat-
accumulation of CalS was maintained but distal cor- ment with LatB caused a progressive redistribution
tical CalS disappeared in conjunction with cytoplas- of CesA (Supplemental Fig. S6B).
mic labeling (asterisk); the taxol effect is also clear in Treatment with inhibitory drugs altered the distri-
time course experiments (Supplemental Fig. S3E). bution of Sus; in untreated tubes, Sus was mainly
These data show that MTs are involved in the distri- found in the apical cortical cytoplasm and to a lesser
bution of CalS in distal regions and, since taxol has extent along the pollen tube shank (Fig. 9D, control).
this effect, not the presence but the dynamics of MTs As already shown (Persia et al., 2008), BFA induced the
are required. All the above-mentioned results were progressive disappearance of Sus from the shank and
consistently observed (at least five independent ex- its accumulation in the tube cytoplasm, suggesting
periments each). To determine quantitatively the that membrane dynamics are required for the delivery
changes in CalS accumulation, the pollen tube was of Sus to the apical membrane and for the maintenance
divided in 10-mm increments along its length and the of Sus in the tube shanks. Indeed, also after treatment
fluorescence intensity resulting from different assays with LatB, Sus progressively disappeared from the
was measured in each region. As observed in the line apical region and accumulated consistently in the tube
graph of Supplemental Figure S4, CalS accumulated shank; signal also extended progressively into the tube
significantly in the cytoplasm after BFA treatment but cytoplasm. Apparently, an intact apical actin cytoskel-
Plant Physiol. Vol. 155, 2011 1181
14. Cai et al.
Figure 9. Distribution of apical vesicles, CalS, CesA , and Sus after treatment with inhibitors. Vesicles were visualized in tobacco
plants expressing a GFP-labeled Rab11b, while CalS, CesA, and Sus were visualized in wild-type tobacco plants. Experimental
conditions were as follows: 5 mg mL21 BFA, 2 nM LatB, 30 mM BDM, 1 mM oryzalin, and 10 mM taxol. A, GFP-labeled Rab11b
showing the distribution of apical vesicles (the arrow in the second image indicates the BFA-induced membrane compartment).
Bar = 10 mm. B, Distribution of CalS after treatment with inhibitors. BFA caused the accumulation of intracellular deposits of CalS
(arrowhead), probably corresponding to BFA-induced aggregates. The three-patterned distribution of CalS was maintained but
was less apparent. LatB affected significantly the distribution of CalS after 15 min (top panel) and more strongly after 30 min
(bottom panel), causing a uniform distribution of CalS in the cortical region and the disappearance of the strong deposits in the
apex. BDM treatment allowed the persistence of lower levels of CalS in the apex but removal of CalS in more distal regions of
pollen tubes. Oryzalin and taxol did not interfere with the apical distribution of CalS but generated the progressive disappearance
of the distal labeled area and the accumulation of intracellular deposits (asterisks). Bar = 10 mm. C, Effects of inhibitors on the
distribution of CesA. BFA induced the accumulation of labeling in the cytoplasm and a consistent decrease in the apical region of
pollen tubes (asterisk). LatB induced a progressive relocation of the CesA signal toward basal regions, although labeling was still
organized as a tip-base gradient. The myosin inhibitor BDM caused a decrease in the accumulation of CesA in the apical/
subapical regions and the progressive disappearance of CesA in distal regions. Oryzalin and taxol caused no significant changes
in the distribution of CesA, which was detected according to the tip-base gradient. Bar = 10 mm. D, Effects of inhibitors on the
distribution of Sus. BFA induced the progressive disappearance of Sus from the tube shanks and its accumulation in the
cytoplasm. LatB induced the progressive disappearance of Sus in the apical domain and accumulation in the base region, with
signal that gradually occupied the tube cytoplasm. BDM treatment caused the persistence of an evident staining in the apex but a
progressive disappearance or absence in the shanks of pollen tubes. Oryzalin and taxol did not have significant effects on the
distribution of Sus. The control pollen tube showed the typical cortical distribution of Sus, with more intense signal in the apex.
Bar = 10 mm. E, Effects of the AF inhibitor LatB. In control pollen tubes (left panel), AFs are typically organized as bundles in distal
regions and as a network in the subapical domain. After treatment with LatB (right panel), bundles of AFs are still present distally
1182 Plant Physiol. Vol. 155, 2011
15. Cellulose, Callose, and Suc Synthase in Pollen Tubes
eton is necessary for the proper delivery of Sus to the in pollen, but it is unclear if the gene codes for the “real”
apex. Inhibition of myosin activity by BDM did not CesA of pollen tubes; in fact, the so-called “cellulose
affect the presence of Sus in the apical region; how- synthase-like” (Csl) genes are structurally related genes
ever, unlike in control pollen tubes, the enzyme was of unknown function that have been hypothesized to
scarcely found in the shank of BDM-treated pollen participate in the synthesis of noncellulosic polysac-
tubes. This suggests that myosin takes part in the charides (Richmond and Somerville, 2000). However,
distribution of Sus in the tube shanks but not in the NaCslD1 contains all the regions typical of plant CesA
apex. Oryzalin did not alter significantly the pattern of proteins, such as the homology domains H-1, H-2, and
Sus, which was still located in the cortex of both apex H-3, the plant-conserved region, and the hypervariable
and tube shanks. Comparable results were obtained in region; the D,D,D,QVLRW motif is also present in the
the presence of taxol; accumulation of Sus in the apical NaCslD1 sequence (Pear et al., 1996). The second gene
domain and in the tube shanks did not show signif- (NaCesA1) is not expressed (or expressed at a very low
icant differences from the control. Figure 9E (right level) in pollen tubes; therefore, its role in the synthesis
panel) shows that oryzalin had induced the disap- of cellulose is questionable. Since CesA sequences (and
pearance of MTs, leaving only fluorescent spots (un- proteins) have not been clearly identified in the pollen
polymerized tubulin). The addition of taxol, which is tube of tobacco, we used an antibody raised against a
known to stabilize MTs, did not affect the MT lattice conserved peptide sequence (NELPRLVYVSREKRPG)
visibly. that is present in both the real nonexpressed NaCesA1
and in the NaCslD1 sequence (although with less
homology). The antigenic peptide sequence is also
DISCUSSION present in the cellulose synthase-like protein CslE
(GenBank accession no. AAZ32787.1) and in the cel-
In this paper, we show that two fundamental en- lulose synthase-like protein CslG (GenBank accession
zymes, CalS and CesA, which are required for the no. AAZ79231.1) of tobacco.
synthesis of cell wall callose and cellulose, respec- Although the biochemistry and subcellular locali-
tively, do not distribute uniformly in the pollen tube zation of CalS in pollen tubes are relatively known,
plasma membrane and that their localization is con- the relationship between CalS, the cytoskeleton, and
trolled by AFs and cortical MTs in different ways. Both membrane dynamics has not been reported. We found
enzymes are present in the pollen tube apex, suggest- the 225-kD CalS polypeptide mainly in association
ing that they deposit callose and CMFs in the pollen with the plasma membrane and cell wall protein
tube tip, where CMFs have been reported to occur fractions of tobacco pollen tubes. Most of the labeling
(Kroh and Knuiman, 1982). A remarkable proportion is associated with the plasma membrane or with the
of CalS is present in distal regions of pollen tubes first nanometers of the cell wall facing it. Assuming the
where callose plugs are being formed and around scale and dimension of gold particles (15 nm) and of
developing callose plugs; distribution of CalS in distal the two antibodies used for indirect immunolabeling,
regions, and therefore in the area where callose plugs a putative distance between the antigen and the center
are formed, seems primarily dependent on MTs, while of gold particles can be estimated around 30 nm
we did not find a dependence of CesA distribution on (Kimura et al., 1999), but the presence of CalS in the
MTs. We further show that cytoplasmic and membrane cell wall could also be caused by the fixation method
Sus bind differently to AFs depending on the Suc used. However, localization of CalS in the plant cell
concentration. wall is not unexpected (Ian et al., 1998) and is also
further supported by immunoblotting on different
Actin Filaments Control the Overall Distribution of protein fractions from tobacco pollen tubes. The local-
CesA, CalS, and Sus in Pollen Tubes ization of tobacco CalS is consistent with its role in
callose production (Brownfield et al., 2008).
In pollen tube rosettes, the CesA-containing com- We tested whether apart from membrane trafficking
plexes (Kimura et al., 1999) have been shown by freeze an intact AF cytoskeleton is required for the maintenance
fracturing (Reiss et al., 1985). Cellulose microfibrils may of CesA and CalS in the apical region. As expected for a
play a critical mechanical role in the apical/subapical plasma membrane protein, BFA accumulated both pro-
region by influencing the diameter of the growing tube teins in intracellular membrane compartments. The BFA
(Kroh and Knuiman, 1982, 1985; Aouar et al., 2010). Two experiments together with electron microscopy images
potential CesA genes have been identified in the pollen show that they travel to the plasma membrane of the
tube of N. alata. The NaCslD1 gene is highly expressed pollen tube tip via Golgi membranes. The AF-depoly-
Figure 9. (Continued.)
but the subapical network disappears. Images are single cortical optical sections. Bars = 10 mm. F, Effects of the MT inhibitor
oryzalin on the organization of MTs in the pollen tube. In controls (left panel), MTs show the typical filamentous arrangement,
which is lost after treatment with oryzalin (right panel), leaving only diffused fluorescent spots. Images are whole cell projections.
Bars = 10 mm.
Plant Physiol. Vol. 155, 2011 1183
16. Cai et al.
merizing drug LatB, which caused disappearance of the MTs. However, we did find aligned CSCs, suggesting
subapical actin fringe, retraction of AF bundles in the that part of them align along MTs. MTs are hardly
´
pollen tube shank, and growth arrest (Cardenas et al., detected in the apex, although the use of GFP-AtEB1
2008), relocates the enzymes progressively backward revealed the presence of dynamic MTs within the
along the tube shank, showing that a proper organization apical domain (Cheung et al., 2008). Therefore, MTs
of AFs is critical for the distribution of CesA and CalS. could regulate the insertion of the membrane contain-
The appearance of intracellular deposits after BFA treat- ing these enzymes in a small defined area in order to
ment is similar to the accumulation of ARA7-labeled regulate the growth of pollen tubes. The interactions
endosomes as observed in Arabidopsis pollen tubes between MTs and CSCs should be further studied in
(Zhang et al., 2010), suggesting that the distribution of more detail in living pollen tubes.
these enzymes is also dependent on a recycling mecha- The evidence that MT inhibitors (taxol and oryzalin)
nism, as has been suggested for CesA by Crowell et al. had no dramatic effects on Sus distribution (coupled
(2009). The role of AFs is confirmed by immunocyto- with the finding that Sus did not bind to MTs and MTs
chemical evidence of the enzymes in association with did not comigrate with Sus in Blue Native-PAGE) shows
vesicular structures close to the plasma membrane (Fig. that the localization of Sus is mainly controlled by AFs.
5, H and I) and by treatment with BDM, which disturbs Distribution of Sus in the plasma membrane is depen-
myosin. Although BDM is reported to cause broad dent on the activity of Golgi membranes, as shown by
effects in plant cells (such as on AFs, cortical endoplas- immunodetection of Sus in a Golgi marker-enriched
mic reticulum, and the MT cytoskeleton; Samaj et al., vesicle fraction and by the disorganization of Sus dis-
2000), current and other reports suggest that cellulose tribution after BFA treatment (Persia et al., 2008; this
(Wightman and Turner, 2008; Crowell et al., 2009; paper). This finding is comparable with the one pro-
Gutierrez et al., 2009) and callose (Chaffey and Barlow, posed to operate in maize, where Sus is enriched in the
2002) synthesis require an acto-myosin mechanism. Golgi system and plasma membranes and is likely to be
BDM does not remove the CesA and CalS already involved in the delivery of substrates to b-glucan syn-
there from the plasma membrane, as is expected. In thase and cellulose synthase (Buckeridge et al., 1999).
addition, labeling is retained in the pollen tube apex,
where the vesicles are located. The different results Microtubules Control the Localization of CalS for Callose
with LatB, which clears the apex from vesicle label Plug Formation in Pollen Tubes
(Fig. 9A), indicate that myosin transports the Golgi
bodies to the subapex but not the Golgi vesicles from CalS is abundantly present in distal regions of the
there to the plasma membrane of the pollen tube tip. pollen tube. A local higher amount of CalS is expected
Actin-myosin interactions appear to be important for to be involved in the synthesis of callose plugs, which
the delivery of the enzymes to the pollen tube subapex is further supported by an increasing concentration of
through Golgi bodies, but Golgi-derived secretory CalS around developing callose plugs. Distal CalS is
vesicles may not depend on this system. slightly affected by LatB treatment, indicating that the
The reaction of organelle and vesicle distribution to mechanism of delivery and accumulation also relates
MT inhibitors indicates that MTs do not take part in the to AFs. MTs appear to be significantly involved in the
delivery of the enzymes to the pollen tube apex. This distribution and maintenance of distal CalS. Asso-
evidence is consistent with data indicating that MTs ciation of MTs with CalS is also supported by Blue
are not critical for the transport of Golgi bodies with Native-PAGE experiments, which indicate that MTs
secretory vesicles to the pollen tube apex (Cai and (but not AFs) can directly bind to CalS. Our data are in
Cresti, 2009, 2010). Analysis of the behavior of yellow agreement with previous observations by Blue Native-
fluorescent protein fused to CesA in transgenic Arabi- PAGE performed in tobacco BY-2 cells (Aidemark
dopsis cells showed that AFs transport CesA-containing et al., 2009). The Blue Native-PAGE experiment sug-
Golgi bodies and deliver them to sites of cell wall gests that insertion of CalS in the plasma membrane
synthesis (Wightman and Turner, 2008). The process of requires the interaction of MTs with membrane-asso-
CSC insertion into the plasma membrane takes place ciated CalS. The drug-mediated removal or stabiliza-
preferably in association with MTs (Gutierrez et al., tion of MTs indeed prevents the correct localization of
2009), although without MTs the insertion of CSCs CalS. Also in BY-2 cells, treatment with oryzalin was
goes on at the same rate as before drug application shown to affect callose deposition (Aidemark et al.,
(Gutierrez et al., 2009). A specific CesA-associated mem- 2009). Current experiments with taxol suggest that the
brane compartment, called the small CesA-containing dynamics of MTs rather than their presence is critical
compartment (Gutierrez et al., 2009) or membrane for the correct localization of distal CalS.
compartments associated with MTs (Crowell et al., In longer tubes, CalS is present at the borders of
2009), was observed to move along depolymerizing growing callose plugs while MTs remain more or less
cortical MTs from which CesA insertion into the longitudinal to the tube’s long axis; this suggests that
plasma membrane took place (Gutierrez et al., 2009). MTs could continuously promote plug growth by
Distribution of CesA in pollen tubes is maintained either repositioning the preexisting CalS at the border
after treatment with either taxol or oryzalin, and we of the growing plug or adding new CalS molecules via
did not find a significant colocalization of CSCs with vesicle delivery. The current literature indicates that an
1184 Plant Physiol. Vol. 155, 2011
17. Cellulose, Callose, and Suc Synthase in Pollen Tubes
intact MT cytoskeleton is required for CalS activity in prisingly, CesA did not accumulate in the callose
Arabidopsis and tobacco BY-2 cells (Aidemark et al., plugs, which supports the evidence that cellulose is
2009), while the synthesis of callose in the liverwort R. not present in the plugs (Ferguson et al., 1998) but only
helicophylla was supposed to depend on the binding of in the original cell wall before plug formation.
CalS to cortical MTs (Scherp et al., 2002). In pollen
tubes of tobacco, depolymerization of MTs by oryzalin Cytoplasmic and Membrane Sus Bind Differently to AFs
caused a considerable reduction in the number of Dependent on the Suc Concentration
callose plugs, indicating that MTs are important for the
proper synthesis of callose in the plugs (Laitiainen Sus is a fundamental enzyme that provides activated
et al., 2002). On the basis of past and current observa- metabolites to CalS and CesA and therefore potentially
tions, we propose the following model (Fig. 10). CalS is controls the synthesis of cellulose and callose (Amor
synthesized in the endoplasmic reticulum and via et al., 1995). The regulatory role of Sus is most likely
Golgi bodies is transported toward the subapex along achieved by finely tuning its partition between a cyto-
AFs. The Golgi-derived vesicles then move to the apex, plasmic form (not involved in the synthesis of cell wall
a process that possibly does not involve myosin. Then, polysaccharides) and a membrane-binding form
the membrane of Golgi vesicles containing CalS is (possibly associated with CesA and CalS). Factors
inserted into the apical plasma membrane, where CalS controlling such a distribution are therefore capable of
starts to produce callose. In the subapex, CalS is regulating cell wall synthesis. Phosphorylation of crit-
removed by endocytosis and eventually recycled; the ical amino acids is one mechanism that possibly reg-
enzyme also might be deactivated (as suggested by ulates the binding of Sus to the plasma membrane
Brownfield et al., 2008). Distally, AFs distribute Golgi (Hardin et al., 2004); other candidates are the concen-
bodies and CalS is inserted into the plasma membrane tration of Suc and the affinity to AFs (Duncan and
by a process mediated by MTs; this hypothesis is Huber, 2007). In a previous paper (Persia et al., 2008),
supported by evidence that in oryzalin-treated tubes, the availability of external Suc was shown to affect the
the number and position of callose plugs are substan- intracellular distribution of Sus in the pollen tube.
tially altered (Laitiainen et al., 2002). Interestingly, the When Suc in the germination medium was replaced
third segment of CalS appears around 100 mm from by glycerol (a nonmetabolizable compound), Sus was
the tube tip (Fig. 2D); the synthesis of callose plugs found at very low levels in the plasma membrane and
is supposed to start in defined areas of the plasma cell wall fractions but at higher levels in the cytoplasm.
membrane where no net flux of H+ occurs (Certal et al., In this work, we show that cytoplasmic and membrane
2008), the first being around 100 mm from the tube tip. Sus bind differently to AFs in the presence of variable
The effects of taxol and oryzalin are rather specific for Suc concentrations. These and past results (Duncan and
CalS, because these drugs caused no significant Huber, 2007) suggest that Sus associates prevalently
changes in the distribution of either CesA or Sus. At with the plasma membrane in the presence of high Suc
the border of developing plugs, the presence of Sus levels. Such an association is probably supported by
increased considerably, indicating that Sus is required dephosphorylation (Persia et al., 2008) and the bind-
for the formation of callose plugs, as expected. Unsur- ing of membrane Sus to AFs and could be a general
Figure 10. Schematic drawing showing the current hypothesis about CalS/CesA insertion into the pollen tube plasma membrane.
CalS and CesA are synthesized in the endoplasmic reticulum (data not shown) and in Golgi bodies transported to the subapex along
bundles of actin filaments (1), from where Golgi vesicles to which Sus also is associated (2) move to the apical plasma membrane
where the vesicle membrane is inserted, including the enzymes (3). In the subapex, the excess of CalS and CesA is removed by
endocytosis and may be eventually recycled (4). Accordingly, a smaller proportion of CalS and CesA persists in the tube (5), although
new insertion of CesA make take place here. Sus might associate with cortical actin filaments, which are used to establish the correct
spatial arrangement. Additional CalS, but not CesA, is inserted into the plasma membrane where a callose plug is formed (6), the
localization of which is determined by microtubules (7). The targets of the inhibitors used are indicated. Objects are not drawn to
scale. Dotted lines indicate that the distance between the apex and the first callose plug is larger than shown.
Plant Physiol. Vol. 155, 2011 1185