Repair and Regeneration Flashcards

1
Q

What are the 3 categories of tissue types based on the regenerative capacity?

A

Labile tissues (with stem cells that continuously cycle to regenerate tissue), stable tissues (can reenter cell cycle to regenerate tissue), permanent tissues without significant ability to regenerate.

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2
Q

What is the name of continuously dividing tissues, and what are 3 examples?

A

Epidermis (stem cells in basal layer), gastrointestinal mucosa (stem cells in crypts) and bone marrow (stem cells in hematopoietic system)

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3
Q

What is the name of tissue that are quiescent but can reenter the cell cycle to regenerate tissue when necessary, and what is an example?

A

Stable tissues. Classic example is liver regeneration after partial resection by compensatory hyperplasia.

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4
Q

What is the name of non-dividing tissues and what are 3 examples?

A

These are permanant tissues and lack signficiant regenerative potential. 3 examples are neurons, myocardium, skeletal muscle.

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5
Q

During tissue repair, what growth factor mediator is an epithelial and fibroblast growth factor?

A

TGF-alpha (also happens to be an attractant for macrophages)

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6
Q

During tissue repair, what growth factor is the most important fibroblast growth factor which also inhibits inflammation?

A

TGF-beta, released by macrophages. It stimulates fibroblasts to lay down collagen (recall that macrophages release TGF-beta and IL-10 to shut down inflammatory response).

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7
Q

During tissue repair, what is the important growth factor for angiogenesis?

A

Vascular endothelial growth factor (VEGF) (also FGF, fibroblast growth factor, promotes angiogenesis and skeletal development)

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8
Q

During tissue repair, what is the growth factor for endothelium, smooth muscle, and fibroblasts, which helps to seal the blood vessel?

A

Platelet derived growth factor

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9
Q

What is the difference between fibrosis and scarring?

A

Fibrosis is the 1. active process that occurs with persistent injury in 2. internal organs in response to chronic injury which 3 involves abnormal deposition of collagen and ECM).
Scarring is the 1. end result of wound healing when 2. inciting agent has been removed or walled off that results in 3. less collagen deposition due to fibroblast quiescence.

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10
Q

What growth factors promote fibroblast migration and proliferation?

A

PDGF, TGF-beta, and FGF are examples.

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11
Q

In wound healing, what is the order of collagen deposition? What removes the first type of collagen, and what is its required cofactor?

A

Collagen III is laid down first, followed by collagen I. Collagenase removes the type III collagen and requires zinc as a cofactor

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12
Q

What tissue type is the initial phase of repair? What does this tissue type contain?

A

Granulation tissue, which contains fibroblasts, capillaries, and myofibroblasts.

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13
Q

After repair, what mediate wound contracture?

A

Myofibroblasts

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14
Q

What is the difference between first intention and second intention?

A

First intention is the wound healing where the wound edges are brought together, leading to minimal scar formation.
Second intention is wound healing where edges are not approximated, so myofibroblasts contract the wound and granulation tissue fills in the defect and forms a large scar.

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15
Q

What are the two major contributors to scarless wound healing in the fetus?

A

Absence of fibrosis and reduced inflammation (fetal TGF-beta receptors in fetus seem to signal less robustly thus reducing fibrosis and fetal IL-10 is increased thus reducing inflammation)

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16
Q

What enzymes are key enzymes that breakdown extracellular matrix and thus keep scarring in check?

A

Metalloproteinases and collagenases

17
Q

What is dehiscence?

A

Separation of tissue edges normally apposed in a surgical incision or repair; involves rupture of the wound

18
Q

What is the difference between a hypertrophic scar and keloid?

A

Both involve an excessive deposition of collagen which results in a raised scar. Hypertrophic scar is characterized by excessive production of type ___ collagen; keloid is excessive production of type ___ collagen (conflicting info from pathoma and first aid)

19
Q

What are adhesions that occur especially in bowel loops?

A

Happens after surgery or infection, abnormal bridging of tissues together via fibrous bands; glues tissues together

20
Q

Why does a vitamin C deficiency lead to impaired wound healing?

A

Vitamin C is required for hydroxylation of proline and lysine procollagen residues, which is required for cross-linking of collagen

21
Q

Why does zinc deficiency lead to impaired wound healing?

A

Zinc is a required cofactor for collagenase which replaces type III collagen with type 1 collagen

22
Q

Why does copper deficiency lead to impaired wound healing?

A

Copper is required cofactor for lysyl oxidase which cross-links lysine and hydroxylysine to form stable collagen

23
Q

What is it called when large wounds contract excessively, and what can this lead to?

A

Called contracture; can lead to joint immobility

24
Q

What are the two types of pathologic calcification?

A

They both result from an abnormal deposit of calcium:

Dystrophic calcification and metastatic calcification

25
Q

What are the expected serum calcium levels in patients with dystrophic calcification and metastatic calcification?

A

Dystrophic calcification is when patients have normal calcium metabolism. Metastatic calcification is when patients have abnormal calcium metabolism and are not normocalcemic (usually secondary to hypercalcemia)

26
Q

In what tissue types does dystrophic and metastatic calcification deposit in?

A

Dystrophic deposits in necrosis or other areas of tissue damage. Metastatic calcification deposits in normal interstitial organs such as gastric mucosa, kidney, or lungs.

27
Q

Would calcification of the arteries due to atherosclerosis be an example of dystrophic calcification or metastatic calcification?

A

Dystrophic calcification

28
Q

What is the abnormality in exuberant granulation (proud flesh)?

A

excess granulation tissue in response to injury which prevents re-epithelialization.