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Tissue Repair
Ghida M Monasar

Presenter by
Supervisor by  Dr . Khadiga mahmoud
Associate professor of pathology
Faculty of medicine & health science
Taiz university
Definition of repair
Is response of living tissue to replace any
surrounding tissue damage .
Is the body’s response to injuries in attempt to
restore normal structure and function .
Is process occur after tissues injury by regenerated
of damage tissues by new healthy one of the
same kind there lost or by deposited another
fibrous tissue (Scar) .
Types of repair
Repair of damaged tissues occurs by two types of
reaction :
1- regeneration  by proliferation of remnant cells
( uninjured ) to replacement dead tissue by the
same kind
2-connective tissue deposition  (scar formation)
- Fibrosis
- gliosis
Determines the types of repair
1 - Cells proliferation
2- Extent of damaged tissue
- severity
- duration
- size
Regeneration
Ability of tissue to replace its damaged components
and essentially return to normal state
That involved :
1- proliferation of cells that depend on capacity to
proliferate
2- interaction between cells ( growth factors )
3- extracellular matrix ECM
1- Cell proliferation
Is a fundamental to development ,
maintenance tissue hemostasis and
replacement of dead or damaged cells .
Cell cycle
G0  cell is out of the cell cycle and don’t dividing
- resting phase –
G1 pre synthetic growth synthesis RNA ,
ribosomes
S DNA synthesis
G2 premitotic growth
M mitotic phase
Cells of the body are divided according to capacity
power of generation in cell cycle into three groups:
1- labile cells
have a high power of regeneration
2- stable cells
have a moderate power of regeneration
3- permanent cells
have No power of regeneration at all
continuous cell )
)
Labile cell
 Cells are constantly being lost ( infected or aging ) and must
be continually replaced by new cells that are derived from
stem cells and rapidly proliferation
As
 Hematopoietic cells in bone marrow
 Surface epithelia of squamous of skin , oral cavity , vagina ,
cervix
 Surface epithelia of cuboidal salivary glands , pancreas ,
biliary tract
 Surface epithelia of columnar gastrointestinal tract ,
endometrium of uterus , fallopian tubes , urinary tact
Quiescent cell )
)
Stable cell
 Cells do not proliferation under normal condition but
proliferate when there need
As
 Parenchyma of solid organs as liver , pancreas , kidney
 Endothelial cells
 Smooth muscle cells
 Bone and cartilage
Permanent cell ( static cell )
 Non proliferate cells can not regeneration
As
 Cardiac muscle
 Skeletal muscle
 Nerve cells
- central nervous ( astrocytes of brain , spinal cord ,ganglia
- but peripheral nervous show limited regeneration as
as schwann cells
2- growth factors
 Growth factor activity is mediated through binding to specific
receptors, that influencing the expression of genes that can:
 1- Promote entry of cells into the cell cycle
 2- blocks on cell cycle and promoting replication
 3-Prevent apoptosis
 4-Enhance biosynthesis of cellular components (nucleic
acids, proteins, lipids, carbohydrates) required for a mother cell
to give rise to two daughter cells
3- extracellular matrix
The ECM is a network of interstitial proteins that
constitutes a significant characteristic of any
tissue.
Cell interactions with ECM are critical for
development and healing,
as well as for maintaining normal tissue
architecture
Liver repair
 mild injury e.g hepatitis A , if the cytoarchitecture is
intact regeneration of hepatocytes with restoration
to normal
Sever injury e.g hepatitis C if the cytoarchitecture
is lose regenerative nodules to show of liver cell
plates and increased fibrosis around nodules lead
to cirrhosis
Regeneration of liver by two major
ways ;
1-from partial hepatectomy
Resection of up to 90% of the liver can be
corrected by proliferation of the remaining
hepatocytes this process controlled by cytokines
IL- 6 that produced by kupffer cells and by growth
factor HGF ( hepatocyte growth factor )
Regeneration of liver by two major
ways
2- from progenitor cells
When proliferative capacity of hepatocytes are
impaired as after chronic liver injury or
inflammation
Progenitor contribute to repopulation called canals
of hering , this topics still active investigation
Factor impair tissue repair
1- infection
is one of the most important causes of delayed repair
2-diabetes
increasing susceptibility to infection and delayed repair
3-nutritional status
Protein malnutrition , vitamin C deficiency that decreased
collagen synthesis
4-mechanical effects
Movements , pressure and torsion delayed repair
5-poor perfusion
Ischemia delayed repair
6-Glucocorticids drugs ( steroids )
that inhibit TGF-B production and interfere collagen formation
delayed and diminish repair
7-extent of tissue injury
types ( mildsever ) and location ( surficial  depth ) of injury
8- foreign bodies
Fragments of glass , wood , …

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Tissue Repair in general pathology important.pdf

  • 1. Tissue Repair Ghida M Monasar Presenter by Supervisor by Dr . Khadiga mahmoud Associate professor of pathology Faculty of medicine & health science Taiz university
  • 2. Definition of repair Is response of living tissue to replace any surrounding tissue damage . Is the body’s response to injuries in attempt to restore normal structure and function . Is process occur after tissues injury by regenerated of damage tissues by new healthy one of the same kind there lost or by deposited another fibrous tissue (Scar) .
  • 3. Types of repair Repair of damaged tissues occurs by two types of reaction : 1- regeneration by proliferation of remnant cells ( uninjured ) to replacement dead tissue by the same kind 2-connective tissue deposition (scar formation) - Fibrosis - gliosis
  • 4.
  • 5. Determines the types of repair 1 - Cells proliferation 2- Extent of damaged tissue - severity - duration - size
  • 6. Regeneration Ability of tissue to replace its damaged components and essentially return to normal state That involved : 1- proliferation of cells that depend on capacity to proliferate 2- interaction between cells ( growth factors ) 3- extracellular matrix ECM
  • 7. 1- Cell proliferation Is a fundamental to development , maintenance tissue hemostasis and replacement of dead or damaged cells .
  • 8.
  • 9. Cell cycle G0 cell is out of the cell cycle and don’t dividing - resting phase – G1 pre synthetic growth synthesis RNA , ribosomes S DNA synthesis G2 premitotic growth M mitotic phase
  • 10. Cells of the body are divided according to capacity power of generation in cell cycle into three groups: 1- labile cells have a high power of regeneration 2- stable cells have a moderate power of regeneration 3- permanent cells have No power of regeneration at all
  • 11. continuous cell ) ) Labile cell  Cells are constantly being lost ( infected or aging ) and must be continually replaced by new cells that are derived from stem cells and rapidly proliferation As  Hematopoietic cells in bone marrow  Surface epithelia of squamous of skin , oral cavity , vagina , cervix  Surface epithelia of cuboidal salivary glands , pancreas , biliary tract  Surface epithelia of columnar gastrointestinal tract , endometrium of uterus , fallopian tubes , urinary tact
  • 12. Quiescent cell ) ) Stable cell  Cells do not proliferation under normal condition but proliferate when there need As  Parenchyma of solid organs as liver , pancreas , kidney  Endothelial cells  Smooth muscle cells  Bone and cartilage
  • 13. Permanent cell ( static cell )  Non proliferate cells can not regeneration As  Cardiac muscle  Skeletal muscle  Nerve cells - central nervous ( astrocytes of brain , spinal cord ,ganglia - but peripheral nervous show limited regeneration as as schwann cells
  • 14. 2- growth factors  Growth factor activity is mediated through binding to specific receptors, that influencing the expression of genes that can:  1- Promote entry of cells into the cell cycle  2- blocks on cell cycle and promoting replication  3-Prevent apoptosis  4-Enhance biosynthesis of cellular components (nucleic acids, proteins, lipids, carbohydrates) required for a mother cell to give rise to two daughter cells
  • 15.
  • 16. 3- extracellular matrix The ECM is a network of interstitial proteins that constitutes a significant characteristic of any tissue. Cell interactions with ECM are critical for development and healing, as well as for maintaining normal tissue architecture
  • 17.
  • 18. Liver repair  mild injury e.g hepatitis A , if the cytoarchitecture is intact regeneration of hepatocytes with restoration to normal Sever injury e.g hepatitis C if the cytoarchitecture is lose regenerative nodules to show of liver cell plates and increased fibrosis around nodules lead to cirrhosis
  • 19.
  • 20. Regeneration of liver by two major ways ; 1-from partial hepatectomy Resection of up to 90% of the liver can be corrected by proliferation of the remaining hepatocytes this process controlled by cytokines IL- 6 that produced by kupffer cells and by growth factor HGF ( hepatocyte growth factor )
  • 21. Regeneration of liver by two major ways 2- from progenitor cells When proliferative capacity of hepatocytes are impaired as after chronic liver injury or inflammation Progenitor contribute to repopulation called canals of hering , this topics still active investigation
  • 22. Factor impair tissue repair 1- infection is one of the most important causes of delayed repair 2-diabetes increasing susceptibility to infection and delayed repair 3-nutritional status Protein malnutrition , vitamin C deficiency that decreased collagen synthesis 4-mechanical effects Movements , pressure and torsion delayed repair 5-poor perfusion Ischemia delayed repair
  • 23. 6-Glucocorticids drugs ( steroids ) that inhibit TGF-B production and interfere collagen formation delayed and diminish repair 7-extent of tissue injury types ( mildsever ) and location ( surficial depth ) of injury 8- foreign bodies Fragments of glass , wood , …