unit 5 Tissue Healing and Repair notes.ppt

Tissue healing and repair

1. TISSUE HEALING AND
REPAIR

2. Overview
Tissuerepairistheresponseoforganismsto
overcomethedamagecausedbytoxicinsults,
inflammationandtrauma.
Inflammatoryresponsedoesnotonlythefirstto
dealwithanytypeoftissueinjury,butalsoinitiates
theprocessofrepairwhichconsistsofthe
restorationoftissuearchitectureandfunction.

3. CELL PROLIFERATION AND
REGENERATION
Tissue repair involves the proliferation of cells
from:
a) the remnants of the injured tissue
b) vascular endothelial cells to form new blood
vessels
c) fibroblasts which provide fibrous tissue for
the formation of scars.

4. •The main steps in the proliferation of cells are
DNA replication and mitosis and this sequence of
events is known as the cell cycle.
•The cell cycle consists of several steps in order
to check the accuracy of cell division.
Non-dividing cells are either in cell cycle arrest in
G1 or they exit the cycle (G0).
Checkpoint controls prevent DNA replication or
mitosis of damaged cells or eliminate damaged
cells by apoptosis.

6. A. Tissue Repair
The ability of tissues to repair themselves depends on
their intrinsic proliferative capacity.
Based on this principle, the tissues of the body can be
divided into three groups:
a) Continuously dividing tissues (labile tissues)
–hematopoietic cells of the bone marrow
–stratified squamous epithelium
–cuboidal epithelium of excretory ducts
–gastrointestinal tract.
These tissues can easily regenerate after injury as
long as stem cells are intact.

7. b) stable tissues–cells of these tissues are quiescent
and have minimal replicate activity. However, cells are
able to replicate in response to injury or loss of tissue
mass.
–parenchyma of most solid organs such as;
–Liver
–Kidney
–Pancreas
–As well as endothelial cells, fibroblasts, and smooth
muscle cells.
With the exception of the liver, stable tissues have a
limited capacity to regenerate.

8. The liver has a great regenerative capacity that occurs
after surgical removal or injury of hepatic tissue.
As much as 40% to 60% of the liver may be removed in a
procedure called living-donor transplantation. In this
situation, replication after partial hepatectomyis
initiated by the cytokines TNF and IL6 that trigger the
transition of hepatocytes from stages g
0to g
1in the cell
cycle.
c) Permanent tissues. The cells of these tissues are
terminally differentiated in post-natal life.
Brain and heart muscle: Results in liquefaction, necrosis
and scar formation.

9. Healed Myocardial Infarct

10. B. Growth Factors
Cell proliferation is triggered by many chemical
mediators such as growth factors, hormones
and cytokines.
Growth factorsare polypeptide molecules
causing an expansion of cell populations which
include an increase in cell size, mitotic activity
and protection from apoptotic death (survival).
In addition to stimulating cellular proliferation,
they promote cellular migration, differentiation,
contractibility, as well as enhancing the
synthesis of special proteins such as collagen by
fibroblasts.

11. C. Repair by Connective Tissue
If extensive tissue surgery is performed or if a
chronic inflammatory process causes damage to
parenchymal cells, epithelia and stromal network,
repair cannot take place by regeneration alone.
The same thing happens when non-dividing cells are
injured. In this situation, repair occurs by replacing
the necrotic tissue with connective tissue or by the
combination of regeneration of some cells and scar
formation.
The extracellular matrix (ECM) is an essential
participant of the repair process.

12. D THE EXTRACELLULAR MATRIX
Divided in two basic forms: interstitial matrix, and basement
membrane.
The interstitial matrixis present in connective tissue
between epithelium and supportive vascular and smooth
muscle structures.
It is synthesized by mesenchymal cells (fibroblasts) and
tends to forms a three-dimensional amorphous gel.
The basement membranelies beneath the epithelium and
is synthesized by overlying epithelium and underlying
mesenchymal cells. It is a highly organized ECM around
epithelial, endothelial, and smooth muscle cells.

13. The ECM has three basic
components:
a) fibrous structural proteins such
as collagens and elastins
b) water hydrated gels,
hyaluronan and proteoglycans
c) adhesive glycoproteins and
adhesion receptors

14. Summary of the roles of the ECM
In addition to filling spaces around cells, the ECM does
the following:
a)Provide mechanical support for cell anchorage,
migration and maintenance of cell polarity.
b) Control of cell growth by signaling through link with
intracellular integrins.
c) Affect the degree of differentiation of the cells in a
given tissue via cell surface integrins.
d) Provide scaffolding for the basement membrane and
interstitial cellular matrix. The integrity of the ECM is
critical for the organized regeneration of
parenchymal cells.

15. e) Establishment of tissue microenvironments. The
basement membrane acts as a boundary between
epithelium and underlying connective tissue.
f) Storage and presentation of regulatory molecules like
growth factors FGF and HGF, synthesize by epithelial
and stromal cells, allowing for rapid deployment of
growth factors after local injury or during
regeneration.

16. Repair by Connective Tissue
It involves the replacement of dead cells and tissues with
connective tissue leading to scar formation. The
sequence of this process is as follows:
1) Repair begins within 24 hours of the time of injury by
the emigration of fibroblasts and the induction of
fibroblast and endothelial cell proliferation.
2) After 3 to 5 days, it begins the formation of granulation
tissue which is pink and soft, with a granular appearance
such as seen underneath the scab of an injured skin.
Histologically, it is composed of proliferating fibroblasts,
newly formed thin capillaries and loose ECM.

17. E. Angiogenesis.
Blood vessels are formed by
vasculogenesis originated by
angioblasts (endothelial precursor
cells (EPCs)) present in the bone
marrow or by neovascularization,
where preexisting blood vessels send
out capillary sprouts to produce new
vessels.

18. Vasculogenesis
The most important
growth factors
involved in
angiogenesis are
VEGF and FGF2.

19. Migration of fibroblasts and ECM
deposition(scar formation).
Scar formation takes place on the
network of the newly formed
granulation tissue and loose ECM. The
scar develops in two steps:
a)Migration and proliferation of
fibroblasts at the injury site, and
b) deposition of ECM by fibroblasts.

20. The fibroblast migration starts early in
wound healing, and continues for several
weeks, depending on the size of the
wound.
As the healing progresses, there is a
decrease of the number of proliferating
fibroblasts and newly formed blood cells
but there is an increase in the deposition
of ECM, particularly collagen.

21. ECM tissue remodeling.
After scar deposition, the ECM continues
to be modified and remodeled. The
outcome of the repair process depends
on the balance between ECM synthesis
and degradation.
The degradation of collagen and ECM is
done by matrix metalloproteinases
(MMPs) which are zinc dependent.

22. Healing by first intention or primary uniontakes place
on wounds with;
focal damage of the basement membrane
death of few epithelial and connective tissue cells.
Here, epithelial regeneration predominates over
fibrosis.
A small scar is formed with minimal wound
contraction.
The whole process is usually completed in two
weeks, with the formation of a thin scar which is
covered by normal epidermis in approximately
one month.

23. Healing by second intentiontakes place when;
cell and tissue loss is extensive, such as large wounds,
abscesses, ulcerations, or ischemic lesions of solid organs.
This healing process is also called secondary union.
a large clot or scab rich in fibrin and plasma fibronectinforms
at the surface of the wound.
The inflammatory response is severe, because large tissue
defects have a great volume of necrotic debris that must
be removed.
A large amount of granulation tissue is formed in order to fill
the gap and to allow regrowth of epithelium and formation
of a usually large scar.
At the end of the process, there is contraction of the wound
(5 to 10% of the original size, brought about by
myofibroblasts).

25. Pathologicaspectsofrepair
Severalconditionsmayalterthe
processofrepair,causingeither
inadequatescarformation,oran
exuberantdepositionofcollagenand
ECM,leadingtotheformationofa
prominentraisedscar.

26. Productionof an inadequate scar or delayin scar formation
may be due to the following:
1) Infection is the most common cause of delay in healing,
by prolonging the inflammatory response and by
increasing local tissue injury.
2) Poor nutrition and specially Vitamin C deficiency
inhibits collagen synthesis and retards healing.
3) Glucocorticoids have a known anti-inflammatory effect
and their administration results in poor wound strength
due to diminished fibrosis.
4) Mechanical variables such as local pressure or torsion
may cause wounds to pull apart or dehisce.

27. 5) Poor perfusion secondary to arteriosclerosis,
diabetes, or obstructive venous drainage also
impairs healing.
6) Foreign bodies like glass fragments, steel fragments,
or bone may disturb healing.
Aberrations of cell growthmay be due to a genetic
predisposition (Keloid formation). This condition is
more common in African American patients.

28. Complications of Repair
Insufficient fibrosis:
Wound dehiscence; hernia; ulceration
Excessive fibrosis:
Cosmetic scarring; hypertrophic scars; keloid
Excessive contraction:
Limitation of joint movement (Contractures); obstruction
of tubes & channels (Strictures

29. Hypertrophic scar

30. Keloid