B cells develop from hematopoietic stem cells in the bone marrow through several stages. Key stages include pro-B cells, pre-B cells, immature B cells, transitional B cells, naive mature B cells, marginal zone B cells, and follicular B cells. Upon activation by antigen, B cells can differentiate into plasmablasts, plasma cells, or memory B cells. Plasma cells migrate to the bone marrow and secrete high amounts of antibody. Dysregulation of B cell differentiation can contribute to autoimmune and alloimmune diseases.
This slide is all about the hematopoeitic stem cells its two types myeloid and lymphoid. The different types of myleoid and lymphoid cells are explained in details. All details about different White Blood Cells and their function. B cell, T cell and Natural Killer cell and their function.
This slide is all about the hematopoeitic stem cells its two types myeloid and lymphoid. The different types of myleoid and lymphoid cells are explained in details. All details about different White Blood Cells and their function. B cell, T cell and Natural Killer cell and their function.
Introduction to Cancer
Stem cells and cancer cells
major pathways that lead to formation of tumors.
Tumor Supressors
Colon cancer to prove Knudson hypothesis.
The modern treatments available to treat cancer.
KEY CONCEPTS
43.1 In innate immunity, recognition and response rely on traits
common to groups of pathogens
43.2 In adaptive immunity, receptors provide pathogen-specific
recognition
43.3 Adaptive immunity defends against infection of body fluids and body cells
43.4 Disruptions in immune system function can elicit or exacerbate disease
Cells lining the inside of cheeks are called as stratified squamous epithelium. They are the surface of the mucous membrane. These flat, scale-like buccal cells are shed constantly as the tissue is renewed. By gently scraping the inside of the cheek, these cells can be harvested and observed under a microscope.
The cells of the immune system can be categorized as lymphocytes (T-cells, B-cells and NK cells), neutrophils, and monocytes/macrophages. These are all types of white blood cells. The major proteins of the immune system are predominantly signaling proteins (often called cytokines), antibodies, and complement proteins.
Introduction to Cancer
Stem cells and cancer cells
major pathways that lead to formation of tumors.
Tumor Supressors
Colon cancer to prove Knudson hypothesis.
The modern treatments available to treat cancer.
KEY CONCEPTS
43.1 In innate immunity, recognition and response rely on traits
common to groups of pathogens
43.2 In adaptive immunity, receptors provide pathogen-specific
recognition
43.3 Adaptive immunity defends against infection of body fluids and body cells
43.4 Disruptions in immune system function can elicit or exacerbate disease
Cells lining the inside of cheeks are called as stratified squamous epithelium. They are the surface of the mucous membrane. These flat, scale-like buccal cells are shed constantly as the tissue is renewed. By gently scraping the inside of the cheek, these cells can be harvested and observed under a microscope.
The cells of the immune system can be categorized as lymphocytes (T-cells, B-cells and NK cells), neutrophils, and monocytes/macrophages. These are all types of white blood cells. The major proteins of the immune system are predominantly signaling proteins (often called cytokines), antibodies, and complement proteins.
The immune system is a complex network of organs, cells and proteins that defends the body against infection, whilst protecting the body’s own cells.
The immune system keeps a record of every germ (microbe) it has ever defeated so it can recognise and destroy the microbe quickly if it enters the body again.
Abnormalities of the immune system can lead to allergic diseases, immunodeficiencies and autoimmune disorders.
On this page
Immune system
The immune system and microbial infection
Parts of the immune system
The body's other defences against microbes
Fever is an immune system response
Common disorders of the immune system
Immunisation
Where to get help
Immune system
The immune system is made up of a complex network of organs, cells and proteins that fight infection (microbes).
The immune system and microbial infection
The immune system keeps a record of every microbe it has ever defeated, in types of white blood cells (B-lymphocytes and T-lymphocytes) known as memory cells. This means it can recognise and destroy the microbe quickly if it enters the body again, before it can multiply and make you feel sick.
Some infections, like the flu and the common cold, have to be fought many times because so many different viruses or strains of the same type of virus can cause these illnesses. Catching a cold or flu from one virus does not give you immunity against the others.wThe immune system is a complex network of organs, cells and proteins that defends the body against infection, whilst protecting the body’s own cells.
The immune system keeps a record of every germ (microbe) it has ever defeated so it can recognise and destroy the microbe quickly if it enters the body again.
Abnormalities of the immune system can lead to allergic diseases, immunodeficiencies and autoimmune disorders.
On this page
Immune system
The immune system and microbial infection
Parts of the immune system
The body's other defences against microbes
Fever is an immune system response
Common disorders of the immune system
Immunisation
Where to get help
Immune system
The immune system is made up of a complex network of organs, cells and proteins that fight infection (microbes).
The immune system and microbial infection
The immune system keeps a record of every microbe it has ever defeated, in types of white blood cells (B-lymphocytes and T-lymphocytes) known as memory cells. This means it can recognise and destroy the microbe quickly if it enters the body again, before it can multiply and make you feel sick.
Some infections, like the flu and the common cold, have to be fought many times because so many different viruses or strains of the same type of virus can cause these illnesses. Catching a cold or flu from one virus does not give you immunity against the others.The immune system is a complex network of organs, cells and proteins that defends the body against infection, whilst protecting the body’s own cells.
The immune system keeps a record of every germ (microbe) it has
B lymphocytes, Receptors, Maturation and ActivationBhanu Krishan
There are two types of lymphocytes namely B-cells and T-cells, which are critical for the immune system.
In addition, several accessory cells and effector cells also participate.
The site of development and maturation of B-cells occurs in bursa fabricius in birds, and bone marrow in mammals. During the course of immune response. B-cells mature into plasma cells and secrete antibodies (immunoglobulins).
The B-cells possess the capability to specifically recognize each antigen and produce antibodies (i.e. immunoglobulins) against it.
The sodium channel is a channel present on the membrane that allows a small amount of Na+ to enter the cell along its electrochemical gradient, as discovered by British scientists Hodgkin and Huxley. It can be divided into two types, voltage-gated and ligand-gated. The sodium ion channel is the primary activation bond for electrical signals in all animals, while the electrical signal is the basis for a series of physiological processes such as neural activity and muscle contraction.
Numerous cells are able to ingest foreign materials, but the ability to increase this activity in response to opsonization by antibody and/or complement, so as to acquire antigen specificity, is restricted to cells of the myeloid series, principally polymorphs, monocytes and macrophages; these are sometimes termed ‘professional’ phagocytes.
Neuroscience is characterized by multi-disciplinary and multi-level intersections. It combines behavior, cognition and brain mechanism, and it attempts to elaborate the neural mechanism of human and animal in perceiving objects, forming images, using language, memorizing information, reasoning and decision-making at the micro level of molecule, synapse and neuron and at the macro level of system, whole brain and behavior.
Transient receptor potenital (TRP) is a large family of non-selective cation channels located on the cell membrane. One type of channel can be activated by Vanillic acid compounds, so this type of channel is called the TRPV subfamily. Mutations in TRPV are associated with neurodegenerative diseases, skeletal dysplasia, kidney disease and cancer and TRPV is an important therapeutic target for these diseases.
CFTR is a chloride channel located on the cell membrane. Under the mediation of cAMP, CFTR is phosphorylated, causing the channel to open and transporting about 10 CIs extracellularly per minute. When the cftr gene is mutated (most commonly, the codon encoding 508 phenylalanine is lost), the defective CFTR cannot be processed normally in the endoplasmic reticulum, and most cannot be transported to the cell membrane;
The organic cation transporter (OCT) is an important drug delivery protein with a broad tissue distribution in the body that mediates the metabolic processes of most drugs. At present, the gene sequence, transport mechanism, substrate structure specificity, regulatory mechanism, gene polymorphism andin vivodistribution characteristics of this transporter have been deeply studied. Based on this knowledge, pharmacologists have successfully delivered many drugs at the transporter molecule level and applied them to clinical practice.
Epigenetics is the study of heritable changes in gene function that do not involve changes in the DNA sequence. A variety of epigenetic mechanisms can be perturbed in different types of cancer. Epigenetic alterations of DNA repair genes or cell cycle control genes are very frequent in sporadic (non-germ line) cancers, being significantly more common than germ line (familial) mutations in these sporadic cancers.
In genetics, genotoxicity describes the property of chemical agents that damage the genetic information within a cell causing mutations(Genotoxicity is often confused with mutagenicity. All mutagens are genotoxic, whereas not all genotoxic substances are mutagenic.). The alteration can have direct or indirect effects on the DNA: the induction of mutations, mistimed event activation, and direct DNA damage resulting in mutations.
The process of cell cycle regulation is the activation or inactivation of various regulatory factors under the surveillance of checkpoints, thereby initiating the process of cell DNA replication and division into two daughter cells.
DNA mismatch repair (MMR) recognizes and repairs erroneous insertion, deletion, and mis-incorporation of bases that can arise during DNA replication and recombination, and repair some forms of DNA damage. It plays an important role in maintaining genomic stability and cellular homeostasis.
Post-translational modifications play an important role in cells, such as DNA recognition, protein-protein interactions, catalytic activity, and protein stability. Protein acetylation/deacetylation is a histone covalent modification that is mainly catalyzed by histone acetylase and histone deacetylase, respectively.
DNA mismatch repair (MMR) recognizes and repairs erroneous insertion, deletion, and mis-incorporation of bases that can arise during DNA replication and recombination, and repair some forms of DNA damage. It plays an important role in maintaining genomic stability and cellular homeostasis.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
DERIVATION OF MODIFIED BERNOULLI EQUATION WITH VISCOUS EFFECTS AND TERMINAL V...Wasswaderrick3
In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
ANAMOLOUS SECONDARY GROWTH IN DICOT ROOTS.pptxRASHMI M G
Abnormal or anomalous secondary growth in plants. It defines secondary growth as an increase in plant girth due to vascular cambium or cork cambium. Anomalous secondary growth does not follow the normal pattern of a single vascular cambium producing xylem internally and phloem externally.
Toxic effects of heavy metals : Lead and Arsenicsanjana502982
Heavy metals are naturally occuring metallic chemical elements that have relatively high density, and are toxic at even low concentrations. All toxic metals are termed as heavy metals irrespective of their atomic mass and density, eg. arsenic, lead, mercury, cadmium, thallium, chromium, etc.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
2. www.creative-diagnostics.com
B cells biology
There still much remains to be understood
about B cell biology in order to determine the
timing, duration, and context of optimal
therapeutic response to B cell-targeted
approaches.
B cells, also known as B lymphocytes, are
primarily generated from hematopoietic stem
cells which play a central role in the immune-
pathogenesis of glomerulonephritides and
transplant rejection.
3. www.creative-diagnostics.com
B cells function
B cells contribute to disease pathogenesis by
providing costimulation and cytokines to T cells. B
cells also play an immunomodulatory role in
regulating the immune response by secreting
cytokines that inhibit disease onset and progression.
B cells can secrete antibodies through multiple
mechanisms and their antibodies are the
central elements of humoral immunity which
against an almost unlimited variety of
pathogens.
The antigen-recognition molecules of B cells are the immunoglobulins
(Ig). These proteins are produced by B cells in a vast range of antigen
specificities, each B cell producing immunoglobulin of a
single specificity.
4. www.creative-diagnostics.com
B cells development
In the earliest B cell lineage, committed precursors
( ) Ig genes exist in a germline configuration.
Early B cell factor 1 (EBF1) is one of the key transcription
factors required for orchestrating B cell lineage
development. During the differentiation of pro-B
cells into cells, a rearrangement in the heavy
chain locus begins in early pro-B cells.
This which typically occurs at both alleles of the heavy-chain
locus, at which point the cell becomes a late pro-B cell. And
then a successful rearrangement means the cell progresses to
become a pre-B cell.
Pro-B cell
CD19+
CD10+
CD34+
IgM-
Pre-B cell
CD19+
CD10+
CD34-
IgM-
EBF1
Bone Marrow(BM)
pro-B cells
pre-B
5. www.creative-diagnostics.com
B cells development
Immature B cell
CD19+
CD10+
CD34-
IgM-
Pro-B cell
CD19+
CD10+
CD34+
IgM-
Pre-B cell
CD19+
CD10+
CD34-
IgM-
EBF1
Bone Marrow(BM)
Mature B cell
CD19+
CD10-
CD34-
IgM++
The chance of generating pre-B cell is less
than 55%.
Once these rearrangements are
successfully completed, transcription
begins and a mature mRNA encoding the μ
heavy chain is produced, which
accumulates in the cytoplasm. Next the
pre-B cells become , and
then develop to .
immature B cells
mature B cells
6. www.creative-diagnostics.com
B cells differentiation
Pro-B cell
CD19+
CD10+
CD34+
IgM-
Pre-B cell
CD19+
CD10+
CD34-
IgM-
EBF1
Immature B cell
CD19+
CD10+
CD34-
IgM-
Bone Marrow(BM)
Mature B cell
CD19+
CD10-
CD34-
IgM++
Igα, Igβ
exit the
bone marrow and enter
the blood to complete
their maturation program
in secondary lymphoid
tissues, preferentially in
the .
Transitional cells then finalize
their maturation process and
give rise to .
T2
CD21
T1
CD21
Transitional B cell
CD19+
CD10+
CD34++
CD24++
Spleen
Naive Mature
B cell
Immature B cells
spleen
naive mature B cells
7. www.creative-diagnostics.com
B cells differentiation
Immature B cell
CD19+
CD10+
CD34-
IgM-
Pro-B cell
CD19+
CD10+
CD34+
IgM-
Pre-B cell
CD19+
CD10+
CD34-
IgM-
EBF1
Bone Marrow(BM)
Mature B cell
CD19+
CD10-
CD34-
IgM++
Igα, Igβ
T1
CD21
T2
CD21
Transitional B cell
CD19+
CD10+
CD34++
CD24++
Spleen
Naive Mature
B cell
Marginal Zone B cell
CD19+
CD23+-
CD21++
Follicular B Cell
CD19+
CD23+-
CD21-/+
Once the immature B cells leave the bone
marrow for the periphery and undergo the
aforementioned transitional stages, they
develop either into or
into .
marginal zone B cells
follicular B cells
8. www.creative-diagnostics.com
B cells differentiation
Immature B cell
CD19+
CD10+
CD34-
IgM-
Pro-B cell
CD19+
CD10+
CD34+
IgM-
Pre-B cell
CD19+
CD10+
CD34-
IgM-
EBF1
Bone Marrow(BM)
Mature B cell
CD19+
CD10-
CD34-
IgM++
Igα, Igβ
The purpose of the germinal center reaction is to enhance the later part of the primary immune
response. Some differentiate first into and then into .
Transitional B cell
CD19+
CD10+
CD34++
CD24++
T1
CD21
T2
CD21
Spleen
Naive Mature
B cell
Marginal Zone B cell
Follicular B Cell
Antibodies
Plasmablast Plasma cell
Germinal CenterPre-GC B cell
germinal center cells plasmablasts plasma cells
9. www.creative-diagnostics.com
B cells differentiation
Immature B cell
CD19+
CD10+
CD34-
IgM-
Pro-B cell
CD19+
CD10+
CD34+
IgM-
Pre-B cell
CD19+
CD10+
CD34-
IgM-
EBF1
Bone Marrow(BM)
Mature B cell
CD19+
CD10-
CD34-
IgM++
Igα, Igβ
Other differentiate into . Memory B cells are long-lived descendants of cells
that were once stimulated by antigen and had proliferated in the . These cells divide very slowly if
at all, and they express surface immunoglobulin, but do not secrete antibody at a high rate.
Marginal Zone B cell
Follicular B Cell
Germinal Center
Transitional B cell
CD19+
CD10+
CD34++
CD24++
T1
CD21
T2
CD21
Spleen
Naive Mature
B cell
Antibodies
Plasmablast Plasma cell
Memory B cell
Switched Unswitched
Pre-GC B cell
germinal center cells memory B cells
germinal center
10. www.creative-diagnostics.com
Plasma cells
• The differentiation of a B cell into a plasma cell is
accompanied by many morphological changes that
reflect its commitment to the production of large
amounts of secreted antibody. Plasma cells have
abundant cytoplasm dominated by multiple layers of
rough endoplasmic reticulum.
These plasma cells will migrate to the bone marrow,
where a subset of them will live for a long period of
time. Plasma cells obtain signals from bone
marrow stromal cells that are essential for their survival.
These plasma cells provide a source of long-lasting high-
affinity antibody.
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Diseases of B cell differentiation
B cells contribute to disease
pathogenesis in autoimmunity and
alloimmunity by presenting antigens
as well as providing costimulation
and cytokines to T cells.
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• Please contact us for more information.
• Email us at info@creative-diagnostics.com
• Website http://www.creative-diagnostics.com/
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We are professional biotech company, specializing
in providing clients comprehensive products related
to B cell differentiation.
A rough estimate of the chance of generating a pre-B cell is thus something less than 55%. Once these rearrangements are successfully completed, transcription begins and a mature mRNA encoding the μ heavy chain is produced, which accumulates in the cytoplasm.
A rough estimate of the chance of generating a pre-B cell is thus something less than 55%. Once these rearrangements are successfully completed, transcription begins and a mature mRNA encoding the μ heavy chain is produced, which accumulates in the cytoplasm.
A rough estimate of the chance of generating a pre-B cell is thus something less than 55%. Once these rearrangements are successfully completed, transcription begins and a mature mRNA encoding the μ heavy chain is produced, which accumulates in the cytoplasm.
A rough estimate of the chance of generating a pre-B cell is thus something less than 55%. Once these rearrangements are successfully completed, transcription begins and a mature mRNA encoding the μ heavy chain is produced, which accumulates in the cytoplasm.
A rough estimate of the chance of generating a pre-B cell is thus something less than 55%. Once these rearrangements are successfully completed, transcription begins and a mature mRNA encoding the μ heavy chain is produced, which accumulates in the cytoplasm.
These plasma cells will migrate to the bone marrow, where a subset of them will live for a long period of time. Plasma cells obtain signals from bone marrow stromal cells that are essential for their survival. These plasma cells provide a source of long-lasting high-affinity antibody.
Vertebrates inevitably die of infection if they are unable to make antibodies. Antibodies defend us against infection by binding to viruses and microbial toxins, thereby inactivating them. The binding of antibodies to invading pathogens also recruits various types of white blood cells and a system of blood proteins collectively called complement. The white blood cells and activated complement components work together to attack the invaders.