SlideShare a Scribd company logo
1 of 26
By
KAUSHAL KUMAR SAHU
Assistant Professor (Ad Hoc)
Department of Biotechnology
Govt. Digvijay Autonomous P. G. College
Raj-Nandgaon ( C. G. )
Contents:
 Introduction
 Definition
 History
 Principle
 Cell sources
 What cells can be used?
 Scaffolds
 Biomaterials
 Bioreactor
 How tissue engineering is done?
 How does tissue engineering differ from cloning?
 Tissue engineering of specific structures
 Application of tissue engineering
 Limitations
 Conclusion
 References
Introduction
 Tissue Engineering is a multidisciplinary field that applies
the principles of Biology, Chemistry, Physics and
Engineering for the development of substitutes that
replace, repair or enhance biological function of diseased
and damaged human body parts, by manipulating cells via
their extracellular microenvironment.

 Tissue Engineering is the study of the growth of new
connective tissues, or organs, from cells and a collagenous
scaffold to produce a fully functional organ for
implantation back into the donor host.

 This technique will allow organs to be grown from
implantation (rather than transplantation) and hence free
from imunological rejection.

Definition
 Broadly defined, tissue engineering is the
development and manipulation of laboratory-grown
molecules, cells, tissues and organs to replace or
support the function of defective or injured body parts.
 Or
 Technology combining genetic engineering of cells
with chemical engineering to create artificial organs
and tissues.

History
 Tissue engineering is a concept originally proposed by
American researchers in 1993, with the purpose of
using living cells to artificially grow tissue and organs
which would then be capable of carrying out their
normal functions.
Principle
Types of cells:
 Autologous: Harvested from patient
 Allogenic: Cells from donor
 Xenogenic: Cells from different species
 Syngeneic cells : which come from genetically
identical individuals
So what cells can be used?
 Cells used in tissue engineering have to be able to
divide in numerous times, so these cells are usually
stem cells.

 Stem cells are undifferentiated cells with the ability to
divide in culture and give rise to different forms of
specialized cells. Stem cells are divided into "adult"
and "embryonic" stem cells, the first class being
multipotent and the latter mostly pluripotent.

 Because stem cells have the ability to form specialized
cells, at the moment they are the best candidate for
tissue engineering .

Scaffolds
 Cells are often implanted or 'seeded' into an artificial
structure capable of supporting three-dimensional tissue
formation & to maintain the structure for tissue
formation.These structures, typically called scaffolds.
 Scaffolds must: Allow cell attachment and migration,
enable transportation of vital cell nutrients, and be
biodegradable.
 Stem cells are seeded into a scaffold.The scaffold is then
implanted into the correct position. A stimulus carried by
the scaffold triggers the cells to divide.The scaffold
provides nutrients and structure while the cells divide.The
scaffold biodegrades as the cells start to form a structure
strong enough to support itself.
Challenges
 In some cases, the scaffold will cause the
degeneration of surrounding tissues.


 Furthermore, scaffolds are many times rejected by
the immune system because it is recognized as a
foreign object

 The process retrieving of cells needed for tissue
engineering can also lead to tissue degeneration.

What can be done to overcome
these obstacles?
 The most promising solution to these obstacles is the SFF (Solid
Freeform) Scaffold.
 Scaffolds may also be constructed from natural materials: in
particular different derivatives of the extracellular matrix have
been studied to evaluate their ability to support cell growth.
Proteic materials, such as collagen or fibrin, and polysaccharidic
materials, like chitosan or glycosaminoglycans (GAGs), have all
proved suitable in terms of cell compatibility.
 The benefit of a collagen scaffold is that the body doesn’t reject
commonly reject it, the process doesn’t denature the collagen due
to high temperature, and offers the possibility of incorporating
biological molecules into the scaffold.

Biomaterials
 Many different materials (natural and synthetic,
biodegradable and permanent) have been
investigated.A commonly used synthetic material
is PLA - polylactic acid. This is a polyester which
degrades within the human body to form lactic
acid, a naturally occurring chemical which is easily
removed from the body. Similar materials are
polyglycolic acid (PGA) and polycaprolactone
(PCL): their degradation mechanism is similar to
that of PLA, but they exhibit respectively a faster
and a slower rate of degradation compared to PLA.
 Natural material:Extracellular Matrix (ECM)
Extarcellular gel-like substance which provides 3D
organization to cells and means of
communication,control of proliferation, cell
migration, attachment,differentiation and repair.
 The ideal biomaterial should be biocompatible in
that it is biodegradable and bioresorbable to
support the replacement of normal tissue without
inflammation.

Bioreactor
 A bioreactor in tissue engineering, as opposed to
industrial bioreactors, is a device that attempts to
simulate a physiological environment in order to
promote cell or tissue growth in vivo. A
physiological environment can consist of many
different parameters such as temperature and
oxygen or carbon dioxide concentration, but can
extend to all kinds of biological, chemical or
mechanical stimuli. Therefore, there are systems
that may include the application of forces or
stresses to the tissue or even of electrical current
in two- or three-dimensional setups.
How tissue engineering is done?
How does tissue engineering
differ from cloning?
 Human cloning is generally used to describe the
isolation of cells from an adult, and extraction of the
nucleus from one of these cells. This nucleus is then
injected into an embryonic cell and therefore all the
embryos derived from this will be identical to the
adult where the first cells are being isolated. This is in
sharp contrast to tissue engineering that aims at using
cells from human tissue - muscle, for example - to
regenerate another human tissue for the repair or
replacement of that tissue. While stem cells can be
used, they are not implanted into embryos, nor is the
goal of tissue engineering to reproduce an exact copy
of the "donor".
Tissue Engineering of Specific
Structures:
 BoneTissue Engineering:
Bone is a critical organ for prevention of injury and support of
normal functions (ambulation, mastication) and is the second
most transplanted tissue (after blood). Autologous bone tissue is
the preferred material for repair of tissue deficits that arise (from
trauma, disease, and birth defects) because the body is capable
of integrating with it, and remodeling it to an essentially normal
tissue.
 Kidney
 We applied the principles of both tissue engineering and
therapeutic cloning in an effort to produce genetically
identical renal tissue in a large animal model, cattle (Bos
taurus). Bovine skin fibroblasts from adult Holstein steers
were obtained by ear notch, and single donor cells were
isolated and microinjected into the perivitelline space of
donor enucleated oocytes (nuclear transfer).The resulting
blastocysts were implanted into progastrin-synchronized
recipients to allow for further in vivo growth. After 12 wk,
cloned renal cells were harvested, expanded in vitro, and
seeded onto biodegradable scaffolds.The constructs, which
consisted of the cells and the scaffolds, were then
implanted into the subcutaneous space of the same steer
from which the cells were cloned to allow for tissue growth.
 BloodVessels
 Tissue-engineered vascular grafts have been
constructed using autologous cells and
biodegradable scaffolds and have been applied in
dog and lamb models .The key advantage from the
use these autografts is that they degrade in vivo and
thus allow the new tissue to form without the long-
term presence of foreign material .
 Bladder
 Currently, gastrointestinal segments are commonly
used as tissues for bladder replacement or repair.
However, gastrointestinal tissues are designed to
absorb specific solutes, whereas bladder tissue is
designed for the excretion of solutes. Because of
the problems encountered with the use of
gastrointestinal segments, numerous investigators
have attempted alternative materials and tissues
for bladder replacement or repair.
Applications of tissue
engineering
 This technology is currently being used to treat
severely burned patients. A small sample of the
patient’s healthy skin is harvested, then grown and
transplanted to the burned areas. But while burn
patients have been benefiting from this type of
treatment for many years, improvements are still
needed to make the transplanted skin identical to
the original skin. Besides skin regeneration,
researchers have been working on a variety of
other applications for tissue engineering :
 Orthopedic:
 Vascular:
 Respiratory
 Ophthalmologic
 Constructing new organs, including liver and bladder
etc.
Limitations of traditional
tissue engineering approaches
 Despite these scientific progresses and clinical outcomes,
engineered tissues and especially thick or complex tissues still
suffer from reoccurring drawbacks:
 cell penetration and adhesion is not very effective.One or
several months might be needed for the cells to adhere and
proliferate into the scaffold.As a result, an incomplete
colonization, limited to the scaffold’s external layers may
occur.
 organs and tissues are generally complex, including
different cell types. Cell-to-cell contact and cell-to-substrate
interaction is critically involved in tissue morphogenesis and
regulation, or healing. Consequently the need to promote
cell-to-cell communication remains a very challenging issue
for this kind of approaches.
Conclusion:
 Tissue engineering is emerging as a vibrant industry
with a huge potential market.The biomaterials,
scaffolds, artificial organs, and differentiating cells
that are combined to create a tissue engineering
product address significant medical needs, such as
major tissue and organ damage or failure.Tissues
like muscle, skin, cardiac cells, nerve, bone,
cartilage have been regenerated by tissue
engineering approach and its application is being
extended for regenerating many more of such
tissues and organs.
References:
 Biotechnology-U.Satyanarayan.
 Net source: www.wikipedia.com
 www.kbiotech.com
 www.science.com

More Related Content

What's hot

TISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACH
TISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACHTISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACH
TISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACHFelix Obi
 
Tissue engineering and stem cell by regenerative medicine.pptx badal 2014
Tissue engineering and stem cell by regenerative medicine.pptx badal 2014Tissue engineering and stem cell by regenerative medicine.pptx badal 2014
Tissue engineering and stem cell by regenerative medicine.pptx badal 2014Pradeep Kumar
 
Bioreactors in tissue engineering
Bioreactors in tissue engineeringBioreactors in tissue engineering
Bioreactors in tissue engineeringEngrMozammelHoque
 
Basics of Tissue engineering
Basics of Tissue engineeringBasics of Tissue engineering
Basics of Tissue engineeringMahmoud Hamda
 
Polymeric and metallic scaffolds for tissue engineering
Polymeric and metallic scaffolds for tissue engineeringPolymeric and metallic scaffolds for tissue engineering
Polymeric and metallic scaffolds for tissue engineeringMohamed M. Abdul-Monem
 
Tissue engineering: AN INTRODUCTION
Tissue engineering: AN INTRODUCTION Tissue engineering: AN INTRODUCTION
Tissue engineering: AN INTRODUCTION Vipin Shukla
 
Stem cells and tissue engineering
Stem cells and tissue engineeringStem cells and tissue engineering
Stem cells and tissue engineeringSandeep Pm
 
Cell synchronization, animal cell culture
Cell  synchronization, animal cell cultureCell  synchronization, animal cell culture
Cell synchronization, animal cell cultureKAUSHAL SAHU
 
bone tissue engineering
bone tissue engineeringbone tissue engineering
bone tissue engineeringSomdutt Sharma
 
Tissue Engineering & Regenerative Medicine
Tissue Engineering & Regenerative MedicineTissue Engineering & Regenerative Medicine
Tissue Engineering & Regenerative MedicineMohamed Labadi
 
Tissue Engineering
Tissue EngineeringTissue Engineering
Tissue Engineeringcindyveloso
 
Stem Cells and Tissue Engineering: past, present and future
Stem Cells and Tissue Engineering: past, present and futureStem Cells and Tissue Engineering: past, present and future
Stem Cells and Tissue Engineering: past, present and futureAna Rita Ramos
 
Tissue engg.
Tissue engg. Tissue engg.
Tissue engg. arushe143
 

What's hot (20)

Tissue engineering
Tissue engineeringTissue engineering
Tissue engineering
 
Tissue engineering
Tissue engineering  Tissue engineering
Tissue engineering
 
TISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACH
TISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACHTISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACH
TISSUE DEVELOPMENT WITH TISSUE ENGINEERING APPROACH
 
Tissue engineering and stem cell by regenerative medicine.pptx badal 2014
Tissue engineering and stem cell by regenerative medicine.pptx badal 2014Tissue engineering and stem cell by regenerative medicine.pptx badal 2014
Tissue engineering and stem cell by regenerative medicine.pptx badal 2014
 
Tissue engineering
Tissue engineeringTissue engineering
Tissue engineering
 
Bioreactors in tissue engineering
Bioreactors in tissue engineeringBioreactors in tissue engineering
Bioreactors in tissue engineering
 
Basics of Tissue engineering
Basics of Tissue engineeringBasics of Tissue engineering
Basics of Tissue engineering
 
TISSUE ENGINEERING
TISSUE ENGINEERINGTISSUE ENGINEERING
TISSUE ENGINEERING
 
3D cell cultures
3D cell cultures3D cell cultures
3D cell cultures
 
Polymeric and metallic scaffolds for tissue engineering
Polymeric and metallic scaffolds for tissue engineeringPolymeric and metallic scaffolds for tissue engineering
Polymeric and metallic scaffolds for tissue engineering
 
Tissue engineering: AN INTRODUCTION
Tissue engineering: AN INTRODUCTION Tissue engineering: AN INTRODUCTION
Tissue engineering: AN INTRODUCTION
 
Tissue engineering
Tissue engineeringTissue engineering
Tissue engineering
 
Tissue engineering
Tissue engineeringTissue engineering
Tissue engineering
 
Stem cells and tissue engineering
Stem cells and tissue engineeringStem cells and tissue engineering
Stem cells and tissue engineering
 
Cell synchronization, animal cell culture
Cell  synchronization, animal cell cultureCell  synchronization, animal cell culture
Cell synchronization, animal cell culture
 
bone tissue engineering
bone tissue engineeringbone tissue engineering
bone tissue engineering
 
Tissue Engineering & Regenerative Medicine
Tissue Engineering & Regenerative MedicineTissue Engineering & Regenerative Medicine
Tissue Engineering & Regenerative Medicine
 
Tissue Engineering
Tissue EngineeringTissue Engineering
Tissue Engineering
 
Stem Cells and Tissue Engineering: past, present and future
Stem Cells and Tissue Engineering: past, present and futureStem Cells and Tissue Engineering: past, present and future
Stem Cells and Tissue Engineering: past, present and future
 
Tissue engg.
Tissue engg. Tissue engg.
Tissue engg.
 

Similar to Tissue engineering 2

Tissue engineering by Anwesha Banerjee
Tissue engineering by Anwesha BanerjeeTissue engineering by Anwesha Banerjee
Tissue engineering by Anwesha BanerjeeAnwesha Banerjee
 
Tissue engineering
Tissue engineeringTissue engineering
Tissue engineeringEmad Ammari
 
Past, Present And Future Of Regenerative Tissue Engineering
Past, Present And Future Of Regenerative Tissue Engineering Past, Present And Future Of Regenerative Tissue Engineering
Past, Present And Future Of Regenerative Tissue Engineering Subhranil Bhattacharjee
 
Tissue ingineering biot
Tissue ingineering biotTissue ingineering biot
Tissue ingineering biottanzeel Rehman
 
Tissue engineering biotechnology
Tissue engineering biotechnologyTissue engineering biotechnology
Tissue engineering biotechnologytanzeel Rehman
 
Tissue engineering applications in urology
Tissue engineering applications in urologyTissue engineering applications in urology
Tissue engineering applications in urologyRoshan Shetty
 
tissueengineeringapplicationsinurology-200716071252.pdf
tissueengineeringapplicationsinurology-200716071252.pdftissueengineeringapplicationsinurology-200716071252.pdf
tissueengineeringapplicationsinurology-200716071252.pdfAnees Puthawala
 
Tissue Engineering Report
Tissue Engineering ReportTissue Engineering Report
Tissue Engineering ReportEiman Rana
 
tissue engineering by sanjana pandey
tissue engineering by sanjana pandeytissue engineering by sanjana pandey
tissue engineering by sanjana pandeySANJANA PANDEY
 
tissue engineering
tissue engineering tissue engineering
tissue engineering boris saha
 
Bone tissue engineering
Bone tissue engineeringBone tissue engineering
Bone tissue engineeringMehdi Chamani
 
#1 principles of tissue engineering
#1 principles of tissue engineering#1 principles of tissue engineering
#1 principles of tissue engineeringRoshan Shetty
 
P1 Tissue engineering abhishek mishra
P1 Tissue engineering abhishek mishraP1 Tissue engineering abhishek mishra
P1 Tissue engineering abhishek mishraAbhishek Mishra
 
Tissue Engineering : Poster
Tissue Engineering : PosterTissue Engineering : Poster
Tissue Engineering : PosterArjun K Gopi
 
Organoids: A Foremost Hope For The Future
Organoids: A Foremost Hope For The FutureOrganoids: A Foremost Hope For The Future
Organoids: A Foremost Hope For The Futureshahin_ahmadian
 

Similar to Tissue engineering 2 (20)

Tissue engineering by Anwesha Banerjee
Tissue engineering by Anwesha BanerjeeTissue engineering by Anwesha Banerjee
Tissue engineering by Anwesha Banerjee
 
Tissue engineering
Tissue engineeringTissue engineering
Tissue engineering
 
Past, Present And Future Of Regenerative Tissue Engineering
Past, Present And Future Of Regenerative Tissue Engineering Past, Present And Future Of Regenerative Tissue Engineering
Past, Present And Future Of Regenerative Tissue Engineering
 
Tissue ingineering biot
Tissue ingineering biotTissue ingineering biot
Tissue ingineering biot
 
Tissue engineering biotechnology
Tissue engineering biotechnologyTissue engineering biotechnology
Tissue engineering biotechnology
 
Tissue engineering
Tissue engineeringTissue engineering
Tissue engineering
 
Cultivos de virus
Cultivos de virusCultivos de virus
Cultivos de virus
 
Tissue engineering applications in urology
Tissue engineering applications in urologyTissue engineering applications in urology
Tissue engineering applications in urology
 
tissueengineeringapplicationsinurology-200716071252.pdf
tissueengineeringapplicationsinurology-200716071252.pdftissueengineeringapplicationsinurology-200716071252.pdf
tissueengineeringapplicationsinurology-200716071252.pdf
 
Tissue Engineering Report
Tissue Engineering ReportTissue Engineering Report
Tissue Engineering Report
 
Stem cell
Stem cellStem cell
Stem cell
 
Stem cell
Stem cellStem cell
Stem cell
 
Stem cell
Stem cellStem cell
Stem cell
 
tissue engineering by sanjana pandey
tissue engineering by sanjana pandeytissue engineering by sanjana pandey
tissue engineering by sanjana pandey
 
tissue engineering
tissue engineering tissue engineering
tissue engineering
 
Bone tissue engineering
Bone tissue engineeringBone tissue engineering
Bone tissue engineering
 
#1 principles of tissue engineering
#1 principles of tissue engineering#1 principles of tissue engineering
#1 principles of tissue engineering
 
P1 Tissue engineering abhishek mishra
P1 Tissue engineering abhishek mishraP1 Tissue engineering abhishek mishra
P1 Tissue engineering abhishek mishra
 
Tissue Engineering : Poster
Tissue Engineering : PosterTissue Engineering : Poster
Tissue Engineering : Poster
 
Organoids: A Foremost Hope For The Future
Organoids: A Foremost Hope For The FutureOrganoids: A Foremost Hope For The Future
Organoids: A Foremost Hope For The Future
 

More from KAUSHAL SAHU

tumor suppressor gene, prb, p53 gene
tumor suppressor gene, prb, p53 genetumor suppressor gene, prb, p53 gene
tumor suppressor gene, prb, p53 geneKAUSHAL SAHU
 
tumor suppressor gene by
tumor suppressor gene bytumor suppressor gene by
tumor suppressor gene byKAUSHAL SAHU
 
tumor suppresor genes
tumor suppresor genestumor suppresor genes
tumor suppresor genesKAUSHAL SAHU
 
tumor suppressor gene, prb, p53
tumor suppressor gene, prb, p53tumor suppressor gene, prb, p53
tumor suppressor gene, prb, p53KAUSHAL SAHU
 
transcription factor by kk sahu
transcription factor by kk sahutranscription factor by kk sahu
transcription factor by kk sahuKAUSHAL SAHU
 
DNA repair by kk sahu
DNA repair by kk sahuDNA repair by kk sahu
DNA repair by kk sahuKAUSHAL SAHU
 
membrane protein, synthesis by
membrane protein, synthesis bymembrane protein, synthesis by
membrane protein, synthesis byKAUSHAL SAHU
 
prokaryotic translation mechinry
prokaryotic translation mechinryprokaryotic translation mechinry
prokaryotic translation mechinryKAUSHAL SAHU
 
translation mechinary
translation mechinarytranslation mechinary
translation mechinaryKAUSHAL SAHU
 
translation cycle, protein synnthesis
translation cycle, protein synnthesistranslation cycle, protein synnthesis
translation cycle, protein synnthesisKAUSHAL SAHU
 
co and post translation modification, by
co and post translation modification, byco and post translation modification, by
co and post translation modification, byKAUSHAL SAHU
 
co and post translation modification
co and post translation modificationco and post translation modification
co and post translation modificationKAUSHAL SAHU
 
Prokaryotic transcription by kk
Prokaryotic transcription by kk Prokaryotic transcription by kk
Prokaryotic transcription by kk KAUSHAL SAHU
 
Enzyme Kinetics and thermodynamic analysis
Enzyme Kinetics and thermodynamic analysisEnzyme Kinetics and thermodynamic analysis
Enzyme Kinetics and thermodynamic analysisKAUSHAL SAHU
 
Chromatin, Organization macromolecule complex
Chromatin, Organization macromolecule complexChromatin, Organization macromolecule complex
Chromatin, Organization macromolecule complexKAUSHAL SAHU
 
Receptor mediated endocytosis by kk
Receptor mediated endocytosis by kkReceptor mediated endocytosis by kk
Receptor mediated endocytosis by kkKAUSHAL SAHU
 
Recepter mediated endocytosis by kk ashu
Recepter mediated endocytosis by kk ashuRecepter mediated endocytosis by kk ashu
Recepter mediated endocytosis by kk ashuKAUSHAL SAHU
 
Protein sorting and targeting
Protein sorting and targetingProtein sorting and targeting
Protein sorting and targetingKAUSHAL SAHU
 
Prokaryotic translation machinery by kk
Prokaryotic translation machinery by kk Prokaryotic translation machinery by kk
Prokaryotic translation machinery by kk KAUSHAL SAHU
 
eukaryotic translation machinery by kk sahu
eukaryotic translation machinery by kk sahueukaryotic translation machinery by kk sahu
eukaryotic translation machinery by kk sahuKAUSHAL SAHU
 

More from KAUSHAL SAHU (20)

tumor suppressor gene, prb, p53 gene
tumor suppressor gene, prb, p53 genetumor suppressor gene, prb, p53 gene
tumor suppressor gene, prb, p53 gene
 
tumor suppressor gene by
tumor suppressor gene bytumor suppressor gene by
tumor suppressor gene by
 
tumor suppresor genes
tumor suppresor genestumor suppresor genes
tumor suppresor genes
 
tumor suppressor gene, prb, p53
tumor suppressor gene, prb, p53tumor suppressor gene, prb, p53
tumor suppressor gene, prb, p53
 
transcription factor by kk sahu
transcription factor by kk sahutranscription factor by kk sahu
transcription factor by kk sahu
 
DNA repair by kk sahu
DNA repair by kk sahuDNA repair by kk sahu
DNA repair by kk sahu
 
membrane protein, synthesis by
membrane protein, synthesis bymembrane protein, synthesis by
membrane protein, synthesis by
 
prokaryotic translation mechinry
prokaryotic translation mechinryprokaryotic translation mechinry
prokaryotic translation mechinry
 
translation mechinary
translation mechinarytranslation mechinary
translation mechinary
 
translation cycle, protein synnthesis
translation cycle, protein synnthesistranslation cycle, protein synnthesis
translation cycle, protein synnthesis
 
co and post translation modification, by
co and post translation modification, byco and post translation modification, by
co and post translation modification, by
 
co and post translation modification
co and post translation modificationco and post translation modification
co and post translation modification
 
Prokaryotic transcription by kk
Prokaryotic transcription by kk Prokaryotic transcription by kk
Prokaryotic transcription by kk
 
Enzyme Kinetics and thermodynamic analysis
Enzyme Kinetics and thermodynamic analysisEnzyme Kinetics and thermodynamic analysis
Enzyme Kinetics and thermodynamic analysis
 
Chromatin, Organization macromolecule complex
Chromatin, Organization macromolecule complexChromatin, Organization macromolecule complex
Chromatin, Organization macromolecule complex
 
Receptor mediated endocytosis by kk
Receptor mediated endocytosis by kkReceptor mediated endocytosis by kk
Receptor mediated endocytosis by kk
 
Recepter mediated endocytosis by kk ashu
Recepter mediated endocytosis by kk ashuRecepter mediated endocytosis by kk ashu
Recepter mediated endocytosis by kk ashu
 
Protein sorting and targeting
Protein sorting and targetingProtein sorting and targeting
Protein sorting and targeting
 
Prokaryotic translation machinery by kk
Prokaryotic translation machinery by kk Prokaryotic translation machinery by kk
Prokaryotic translation machinery by kk
 
eukaryotic translation machinery by kk sahu
eukaryotic translation machinery by kk sahueukaryotic translation machinery by kk sahu
eukaryotic translation machinery by kk sahu
 

Recently uploaded

TOTAL CHOLESTEROL (lipid profile test).pptx
TOTAL CHOLESTEROL (lipid profile test).pptxTOTAL CHOLESTEROL (lipid profile test).pptx
TOTAL CHOLESTEROL (lipid profile test).pptxdharshini369nike
 
Artificial Intelligence In Microbiology by Dr. Prince C P
Artificial Intelligence In Microbiology by Dr. Prince C PArtificial Intelligence In Microbiology by Dr. Prince C P
Artificial Intelligence In Microbiology by Dr. Prince C PPRINCE C P
 
Harmful and Useful Microorganisms Presentation
Harmful and Useful Microorganisms PresentationHarmful and Useful Microorganisms Presentation
Harmful and Useful Microorganisms Presentationtahreemzahra82
 
Gas_Laws_powerpoint_notes.ppt for grade 10
Gas_Laws_powerpoint_notes.ppt for grade 10Gas_Laws_powerpoint_notes.ppt for grade 10
Gas_Laws_powerpoint_notes.ppt for grade 10ROLANARIBATO3
 
SOLUBLE PATTERN RECOGNITION RECEPTORS.pptx
SOLUBLE PATTERN RECOGNITION RECEPTORS.pptxSOLUBLE PATTERN RECOGNITION RECEPTORS.pptx
SOLUBLE PATTERN RECOGNITION RECEPTORS.pptxkessiyaTpeter
 
‏‏VIRUS - 123455555555555555555555555555555555555555
‏‏VIRUS -  123455555555555555555555555555555555555555‏‏VIRUS -  123455555555555555555555555555555555555555
‏‏VIRUS - 123455555555555555555555555555555555555555kikilily0909
 
Module 4: Mendelian Genetics and Punnett Square
Module 4:  Mendelian Genetics and Punnett SquareModule 4:  Mendelian Genetics and Punnett Square
Module 4: Mendelian Genetics and Punnett SquareIsiahStephanRadaza
 
Vision and reflection on Mining Software Repositories research in 2024
Vision and reflection on Mining Software Repositories research in 2024Vision and reflection on Mining Software Repositories research in 2024
Vision and reflection on Mining Software Repositories research in 2024AyushiRastogi48
 
Manassas R - Parkside Middle School 🌎🏫
Manassas R - Parkside Middle School 🌎🏫Manassas R - Parkside Middle School 🌎🏫
Manassas R - Parkside Middle School 🌎🏫qfactory1
 
Forest laws, Indian forest laws, why they are important
Forest laws, Indian forest laws, why they are importantForest laws, Indian forest laws, why they are important
Forest laws, Indian forest laws, why they are importantadityabhardwaj282
 
Dashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tanta
Dashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tantaDashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tanta
Dashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tantaPraksha3
 
RESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptx
RESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptxRESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptx
RESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptxFarihaAbdulRasheed
 
zoogeography of pakistan.pptx fauna of Pakistan
zoogeography of pakistan.pptx fauna of Pakistanzoogeography of pakistan.pptx fauna of Pakistan
zoogeography of pakistan.pptx fauna of Pakistanzohaibmir069
 
Behavioral Disorder: Schizophrenia & it's Case Study.pdf
Behavioral Disorder: Schizophrenia & it's Case Study.pdfBehavioral Disorder: Schizophrenia & it's Case Study.pdf
Behavioral Disorder: Schizophrenia & it's Case Study.pdfSELF-EXPLANATORY
 
Speech, hearing, noise, intelligibility.pptx
Speech, hearing, noise, intelligibility.pptxSpeech, hearing, noise, intelligibility.pptx
Speech, hearing, noise, intelligibility.pptxpriyankatabhane
 
Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |
Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |
Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |aasikanpl
 
Spermiogenesis or Spermateleosis or metamorphosis of spermatid
Spermiogenesis or Spermateleosis or metamorphosis of spermatidSpermiogenesis or Spermateleosis or metamorphosis of spermatid
Spermiogenesis or Spermateleosis or metamorphosis of spermatidSarthak Sekhar Mondal
 
Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.
Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.
Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.aasikanpl
 

Recently uploaded (20)

TOTAL CHOLESTEROL (lipid profile test).pptx
TOTAL CHOLESTEROL (lipid profile test).pptxTOTAL CHOLESTEROL (lipid profile test).pptx
TOTAL CHOLESTEROL (lipid profile test).pptx
 
Artificial Intelligence In Microbiology by Dr. Prince C P
Artificial Intelligence In Microbiology by Dr. Prince C PArtificial Intelligence In Microbiology by Dr. Prince C P
Artificial Intelligence In Microbiology by Dr. Prince C P
 
Harmful and Useful Microorganisms Presentation
Harmful and Useful Microorganisms PresentationHarmful and Useful Microorganisms Presentation
Harmful and Useful Microorganisms Presentation
 
Gas_Laws_powerpoint_notes.ppt for grade 10
Gas_Laws_powerpoint_notes.ppt for grade 10Gas_Laws_powerpoint_notes.ppt for grade 10
Gas_Laws_powerpoint_notes.ppt for grade 10
 
SOLUBLE PATTERN RECOGNITION RECEPTORS.pptx
SOLUBLE PATTERN RECOGNITION RECEPTORS.pptxSOLUBLE PATTERN RECOGNITION RECEPTORS.pptx
SOLUBLE PATTERN RECOGNITION RECEPTORS.pptx
 
‏‏VIRUS - 123455555555555555555555555555555555555555
‏‏VIRUS -  123455555555555555555555555555555555555555‏‏VIRUS -  123455555555555555555555555555555555555555
‏‏VIRUS - 123455555555555555555555555555555555555555
 
Module 4: Mendelian Genetics and Punnett Square
Module 4:  Mendelian Genetics and Punnett SquareModule 4:  Mendelian Genetics and Punnett Square
Module 4: Mendelian Genetics and Punnett Square
 
Vision and reflection on Mining Software Repositories research in 2024
Vision and reflection on Mining Software Repositories research in 2024Vision and reflection on Mining Software Repositories research in 2024
Vision and reflection on Mining Software Repositories research in 2024
 
Manassas R - Parkside Middle School 🌎🏫
Manassas R - Parkside Middle School 🌎🏫Manassas R - Parkside Middle School 🌎🏫
Manassas R - Parkside Middle School 🌎🏫
 
Forest laws, Indian forest laws, why they are important
Forest laws, Indian forest laws, why they are importantForest laws, Indian forest laws, why they are important
Forest laws, Indian forest laws, why they are important
 
Volatile Oils Pharmacognosy And Phytochemistry -I
Volatile Oils Pharmacognosy And Phytochemistry -IVolatile Oils Pharmacognosy And Phytochemistry -I
Volatile Oils Pharmacognosy And Phytochemistry -I
 
Dashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tanta
Dashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tantaDashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tanta
Dashanga agada a formulation of Agada tantra dealt in 3 Rd year bams agada tanta
 
Engler and Prantl system of classification in plant taxonomy
Engler and Prantl system of classification in plant taxonomyEngler and Prantl system of classification in plant taxonomy
Engler and Prantl system of classification in plant taxonomy
 
RESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptx
RESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptxRESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptx
RESPIRATORY ADAPTATIONS TO HYPOXIA IN HUMNAS.pptx
 
zoogeography of pakistan.pptx fauna of Pakistan
zoogeography of pakistan.pptx fauna of Pakistanzoogeography of pakistan.pptx fauna of Pakistan
zoogeography of pakistan.pptx fauna of Pakistan
 
Behavioral Disorder: Schizophrenia & it's Case Study.pdf
Behavioral Disorder: Schizophrenia & it's Case Study.pdfBehavioral Disorder: Schizophrenia & it's Case Study.pdf
Behavioral Disorder: Schizophrenia & it's Case Study.pdf
 
Speech, hearing, noise, intelligibility.pptx
Speech, hearing, noise, intelligibility.pptxSpeech, hearing, noise, intelligibility.pptx
Speech, hearing, noise, intelligibility.pptx
 
Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |
Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |
Call Us ≽ 9953322196 ≼ Call Girls In Lajpat Nagar (Delhi) |
 
Spermiogenesis or Spermateleosis or metamorphosis of spermatid
Spermiogenesis or Spermateleosis or metamorphosis of spermatidSpermiogenesis or Spermateleosis or metamorphosis of spermatid
Spermiogenesis or Spermateleosis or metamorphosis of spermatid
 
Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.
Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.
Call Girls in Munirka Delhi 💯Call Us 🔝9953322196🔝 💯Escort.
 

Tissue engineering 2

  • 1. By KAUSHAL KUMAR SAHU Assistant Professor (Ad Hoc) Department of Biotechnology Govt. Digvijay Autonomous P. G. College Raj-Nandgaon ( C. G. )
  • 2. Contents:  Introduction  Definition  History  Principle  Cell sources  What cells can be used?  Scaffolds  Biomaterials  Bioreactor  How tissue engineering is done?  How does tissue engineering differ from cloning?  Tissue engineering of specific structures  Application of tissue engineering  Limitations  Conclusion  References
  • 3. Introduction  Tissue Engineering is a multidisciplinary field that applies the principles of Biology, Chemistry, Physics and Engineering for the development of substitutes that replace, repair or enhance biological function of diseased and damaged human body parts, by manipulating cells via their extracellular microenvironment.   Tissue Engineering is the study of the growth of new connective tissues, or organs, from cells and a collagenous scaffold to produce a fully functional organ for implantation back into the donor host.   This technique will allow organs to be grown from implantation (rather than transplantation) and hence free from imunological rejection. 
  • 4. Definition  Broadly defined, tissue engineering is the development and manipulation of laboratory-grown molecules, cells, tissues and organs to replace or support the function of defective or injured body parts.  Or  Technology combining genetic engineering of cells with chemical engineering to create artificial organs and tissues. 
  • 5. History  Tissue engineering is a concept originally proposed by American researchers in 1993, with the purpose of using living cells to artificially grow tissue and organs which would then be capable of carrying out their normal functions.
  • 7. Types of cells:  Autologous: Harvested from patient  Allogenic: Cells from donor  Xenogenic: Cells from different species  Syngeneic cells : which come from genetically identical individuals
  • 8. So what cells can be used?  Cells used in tissue engineering have to be able to divide in numerous times, so these cells are usually stem cells.   Stem cells are undifferentiated cells with the ability to divide in culture and give rise to different forms of specialized cells. Stem cells are divided into "adult" and "embryonic" stem cells, the first class being multipotent and the latter mostly pluripotent.   Because stem cells have the ability to form specialized cells, at the moment they are the best candidate for tissue engineering . 
  • 9. Scaffolds  Cells are often implanted or 'seeded' into an artificial structure capable of supporting three-dimensional tissue formation & to maintain the structure for tissue formation.These structures, typically called scaffolds.  Scaffolds must: Allow cell attachment and migration, enable transportation of vital cell nutrients, and be biodegradable.  Stem cells are seeded into a scaffold.The scaffold is then implanted into the correct position. A stimulus carried by the scaffold triggers the cells to divide.The scaffold provides nutrients and structure while the cells divide.The scaffold biodegrades as the cells start to form a structure strong enough to support itself.
  • 10.
  • 11. Challenges  In some cases, the scaffold will cause the degeneration of surrounding tissues.    Furthermore, scaffolds are many times rejected by the immune system because it is recognized as a foreign object   The process retrieving of cells needed for tissue engineering can also lead to tissue degeneration. 
  • 12. What can be done to overcome these obstacles?  The most promising solution to these obstacles is the SFF (Solid Freeform) Scaffold.  Scaffolds may also be constructed from natural materials: in particular different derivatives of the extracellular matrix have been studied to evaluate their ability to support cell growth. Proteic materials, such as collagen or fibrin, and polysaccharidic materials, like chitosan or glycosaminoglycans (GAGs), have all proved suitable in terms of cell compatibility.  The benefit of a collagen scaffold is that the body doesn’t reject commonly reject it, the process doesn’t denature the collagen due to high temperature, and offers the possibility of incorporating biological molecules into the scaffold. 
  • 13. Biomaterials  Many different materials (natural and synthetic, biodegradable and permanent) have been investigated.A commonly used synthetic material is PLA - polylactic acid. This is a polyester which degrades within the human body to form lactic acid, a naturally occurring chemical which is easily removed from the body. Similar materials are polyglycolic acid (PGA) and polycaprolactone (PCL): their degradation mechanism is similar to that of PLA, but they exhibit respectively a faster and a slower rate of degradation compared to PLA.
  • 14.  Natural material:Extracellular Matrix (ECM) Extarcellular gel-like substance which provides 3D organization to cells and means of communication,control of proliferation, cell migration, attachment,differentiation and repair.  The ideal biomaterial should be biocompatible in that it is biodegradable and bioresorbable to support the replacement of normal tissue without inflammation. 
  • 15. Bioreactor  A bioreactor in tissue engineering, as opposed to industrial bioreactors, is a device that attempts to simulate a physiological environment in order to promote cell or tissue growth in vivo. A physiological environment can consist of many different parameters such as temperature and oxygen or carbon dioxide concentration, but can extend to all kinds of biological, chemical or mechanical stimuli. Therefore, there are systems that may include the application of forces or stresses to the tissue or even of electrical current in two- or three-dimensional setups.
  • 17. How does tissue engineering differ from cloning?  Human cloning is generally used to describe the isolation of cells from an adult, and extraction of the nucleus from one of these cells. This nucleus is then injected into an embryonic cell and therefore all the embryos derived from this will be identical to the adult where the first cells are being isolated. This is in sharp contrast to tissue engineering that aims at using cells from human tissue - muscle, for example - to regenerate another human tissue for the repair or replacement of that tissue. While stem cells can be used, they are not implanted into embryos, nor is the goal of tissue engineering to reproduce an exact copy of the "donor".
  • 18. Tissue Engineering of Specific Structures:  BoneTissue Engineering: Bone is a critical organ for prevention of injury and support of normal functions (ambulation, mastication) and is the second most transplanted tissue (after blood). Autologous bone tissue is the preferred material for repair of tissue deficits that arise (from trauma, disease, and birth defects) because the body is capable of integrating with it, and remodeling it to an essentially normal tissue.
  • 19.  Kidney  We applied the principles of both tissue engineering and therapeutic cloning in an effort to produce genetically identical renal tissue in a large animal model, cattle (Bos taurus). Bovine skin fibroblasts from adult Holstein steers were obtained by ear notch, and single donor cells were isolated and microinjected into the perivitelline space of donor enucleated oocytes (nuclear transfer).The resulting blastocysts were implanted into progastrin-synchronized recipients to allow for further in vivo growth. After 12 wk, cloned renal cells were harvested, expanded in vitro, and seeded onto biodegradable scaffolds.The constructs, which consisted of the cells and the scaffolds, were then implanted into the subcutaneous space of the same steer from which the cells were cloned to allow for tissue growth.
  • 20.  BloodVessels  Tissue-engineered vascular grafts have been constructed using autologous cells and biodegradable scaffolds and have been applied in dog and lamb models .The key advantage from the use these autografts is that they degrade in vivo and thus allow the new tissue to form without the long- term presence of foreign material .
  • 21.  Bladder  Currently, gastrointestinal segments are commonly used as tissues for bladder replacement or repair. However, gastrointestinal tissues are designed to absorb specific solutes, whereas bladder tissue is designed for the excretion of solutes. Because of the problems encountered with the use of gastrointestinal segments, numerous investigators have attempted alternative materials and tissues for bladder replacement or repair.
  • 22. Applications of tissue engineering  This technology is currently being used to treat severely burned patients. A small sample of the patient’s healthy skin is harvested, then grown and transplanted to the burned areas. But while burn patients have been benefiting from this type of treatment for many years, improvements are still needed to make the transplanted skin identical to the original skin. Besides skin regeneration, researchers have been working on a variety of other applications for tissue engineering :
  • 23.  Orthopedic:  Vascular:  Respiratory  Ophthalmologic  Constructing new organs, including liver and bladder etc.
  • 24. Limitations of traditional tissue engineering approaches  Despite these scientific progresses and clinical outcomes, engineered tissues and especially thick or complex tissues still suffer from reoccurring drawbacks:  cell penetration and adhesion is not very effective.One or several months might be needed for the cells to adhere and proliferate into the scaffold.As a result, an incomplete colonization, limited to the scaffold’s external layers may occur.  organs and tissues are generally complex, including different cell types. Cell-to-cell contact and cell-to-substrate interaction is critically involved in tissue morphogenesis and regulation, or healing. Consequently the need to promote cell-to-cell communication remains a very challenging issue for this kind of approaches.
  • 25. Conclusion:  Tissue engineering is emerging as a vibrant industry with a huge potential market.The biomaterials, scaffolds, artificial organs, and differentiating cells that are combined to create a tissue engineering product address significant medical needs, such as major tissue and organ damage or failure.Tissues like muscle, skin, cardiac cells, nerve, bone, cartilage have been regenerated by tissue engineering approach and its application is being extended for regenerating many more of such tissues and organs.
  • 26. References:  Biotechnology-U.Satyanarayan.  Net source: www.wikipedia.com  www.kbiotech.com  www.science.com