repair and regeneration Flashcards

1
Q

After tissue is damaged it undergoes inflammation and then healing
what are the 2 main types of healing

A

regeneration

repair

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2
Q

define regeneration

A

damaged cells are replaced and return to normal.

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3
Q

define repair

A

damaged cells cannot be replaced so they undergo fibrosis and scaring.

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4
Q

what are the 3 types of cell population

A

Liable cell population
Stable cell population
Permanent cell population

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5
Q

what does liable cell population mean

A

always regenerate.
High normal turnover- to maintain integrity.
Active stem cell population
Excellent regenerative capacity

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6
Q

give an example of a liable cell population

A

epithelial cells.

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7
Q

what does stable cell population mean

A
(quiescent) cell populations
can regenerate if need be.
Low physiological turnover
Turnover can massively increase if needed.
Good regenerative capacity.
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8
Q

give an example of a stable cell population

A

liver and renal tubules.

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9
Q

what does permanent cell population mean

A

No physiological turnover
Long life cells
No regenerative capacity (nb recent stem cell research)

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10
Q

give an example of a permanent cell population

A

eg neurons, muscle cells

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11
Q

Why the architecture of the damaged tissue needed to be present in order for cells to proliferate and replace those which are lost

A

It enables cells to replace those lost in an order fashion so that the organ or tissue can retain it’s function.

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12
Q

Give an example of a condition where the tissue loses it architecture and cannot be replaced.

A

eg cirrhosis.- There is collapse of the reticulin (connective tissue) framework of the liver so that regeneration of liver cells cannot repopulate the normal architecture. This leads to the formation of regenerative nodules divided by fibrous septa.

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13
Q

what are the key properties of stem cells

A

prolonged self renewal
asymmetric replication
reservoirs present in many adult tissues.

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14
Q

what are the 4 main stages in self renewal and differentiation.

A

stem cell compartment
amplifying cell compartment
Differentiating compartment
Terminal differentiation.

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15
Q

what injury can cause damage to the stem cell compartment.

A

full thickness burns, radiation.

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16
Q

what are the functional consequences of repair by fibrosis of the heart post MI

A

Mechanical- loss of pumping capacity
Electrical-arrhythmia or might disrupt the cardiac conducting system if in a critical point (eg His bundles), giving heart block.

17
Q

what factors help to control hyper proliferation.

A

Covering of defect
Contact inhibition
Complex control by growth factors, cell-cell and cell-matrix interactions

18
Q

what are the components of newly formed granulation tissue.

A

New capillaries- so macrophages and neutrophils can get to the tissue.
Phagocytic cells- neutrophils (acute) and macrophages (chronic). Initially neutrophils move in and then macrophages move into tissue if need- they remove dead tissue.
Myo) fibroblasts- produce collagen, and if myo they have myelin which is used to contract the tissue

19
Q

why do we have new capillaries in granulation tissue.

A

so macrophages and neutrophils can get to the tissue.

20
Q

which cells come in first neutrophils or macrophages

A

neutrophils.

21
Q

what is the function of myofibroblasts

A

Produce collagen, and if myo they have myelin which is used to contract the tissue

22
Q

As granulation tissue matures 3 changes take place, these are

A

vascularity and cellularity decrease

Collagen and wound strength increases

23
Q

what local factors inhibit the healing process

A

infection, haematoma, blood supply, foreign bodies, mechanical stress.

24
Q

what systemic factors inhibit the healing process.

A

Age, drugs, anaemia, diabetes, malnutrition, catabolic states, vitamin C deficiency, trace metal deficiency.

25
Q

why does a catabolic state now allow healing to take place

A

breaks down proteins.

26
Q

what is wound healing by primary intention

A

Clean, uninfected surgical wound
Good haemostasis
Edges apposed eg with sutures or staples

27
Q

what is wound healing by secondary intention.

A

Wound edges not apposed- not together

  1. Extensive loss of tissue
  2. Apposition not physically possible
  3. Large haematoma
  4. Infection
  5. Foreign body
28
Q

which has more granulation and scarring- healing by primary or healing by secondary intention

A

healing by secondary intention.

29
Q

what immune cell removes death tissue and scar tissue from a granulation

A

macrophages

30
Q

Be`fore granulation what forms at the site of injury

A

fibroclot.

31
Q

when a bone is fractured what process commonly occurs at the site of injury

A

Haematoma.

32
Q

Is the haematoma following fracture injury organised or not

A

yes it is organised.

33
Q

How is bone reformed at the site of feature an haematoma.

A

Osteoblasts (specialized cells) lay down woven bone
(=callus)
• Remodelling according to mechanical stress
Replacement by lamellar bone

34
Q

what pathological process takes place in the brain following injury

A

Gliosis rather than scarring- due to proliferation of reactive astrocytes.
damaged tissue is often removed leaving a cyst.

35
Q

Is healing a controlled process.

A

Yes- tightly controlled by a complex network of cytokines

36
Q

why is linking healing with cancer important.

A

control of healing molecules are targets for cancer, as tumours must generate a new blood supply and supporting stroma (Which occurs in granulation)

37
Q

supporting cell in normal tissue are collagen and fibroblast, what are the supporting cells in the brian

A

glial cells.

38
Q

targets for cancer treatment include

A

VEGF- vasculognesis
EGF
PDGF
TGF-B

39
Q

what often happens to tissue which undergoes healing by secondary intention

A

undergoes contraction.