Lecture 6 Flashcards

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1
Q

functions of the skin (5)

A
  • protects underlying structures
  • first line of defense from external factors
  • insulation / T regulation
  • sensation (touch, pain, …)
  • production of Vitamin D
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2
Q

most outer layer of skin : main cells, vascularized?

A

Epidermis.
Keratinocytes (also melanocytes and langerhans cells)
No blood vessels.

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3
Q

layers of the epidermis ?

A

differently differentiated keratonicytes : on top, dead cells filled with keratin

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4
Q

second layer of skin : function, main cells, vascularized ?

A

Dermis.
Cushions body from stress and strain (ECM).
Fibroblasts (and immune cells).
Contains blood vessels .

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5
Q

third layer : role, main cells

A

Subcutaneous tissue (NOT part of skin).
Attaches skin to muscle / bone and supplies skin with vessels and nerves.
Main cells are adipocytes (also fibroblasts and macrophages)

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6
Q

classification of wounds

A

superificial, partial thickness, full thickness, deep wound, complex wound, penetrating wound

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7
Q

differences between regeneration, repair, and fibrosis

A

1) regeneration : complete restoration of original tissue, function and structure (minor injuries) -> goal of surgical procedures
2) repair : tissues don’t return to original architecture (scar tissue)
3) fibrosis : after chronic tissue damage -> loss of function

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8
Q

first phase of skin wound healing : name, 3 steps, cells involved

A

Hemostasis.
i) vasoconstriction : cell membrane releases factors that cause vessels to constrict + recruit cells

ii) platelet plug formation : platelets activate (change shape, adhere to collagen and express receptors that creates an aggregation)

iii) clot formation : prothrombin becomes thrombin -> causes fibrinogen to become fibrin -> fibrin matrix that stabilizes the wound and provides a scaffold, clot fills with red blood cells and seals the wound (protection)

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9
Q

second stage of wound healing : name, steps (3), cells involved

A

Inflammation.
Mast cells release granules (with histamine) that causes vasodilation -> redness, heat, swelling, pain.

Early : neutrophils ; only stay a couple days, remove dead tissue and bacteria, replaced by macrophages

Late : macrophages ; phagocytosis -> wound decontamination, regulation of tissue repair, remain until healing complete

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10
Q

what is it called when neutrophils migrate to the wound site ? 4 steps

A

Neutrohil extravasation.
Margination, pavementing, rolling and adhesion, transmigration

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11
Q

5 phases of phagocytosis

A

1) attachment : receptors recognize bacterial cell wall
2) engulfment : phagosome
3) degranulation : phagolysosome
4) degradation : lysosome digests bacteria
5) exocytosis : of digestion products

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12
Q

third stage of wound healing : name, type of tissue, 3 key processes

A

Proliferation.
Granulation tissue if formed : fragile connective tissue (collagen type III) and microscopic blood vessels (angiogenesis)

Fibroplasia : proliferation of fibroblasts that produce matrix and differentiate into myofibroblasts (contract and close the wound)

Epithelialization : proliferation of outer-lining epithelial cells

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13
Q

fourth phase of wound healing : name, 2 steps, result

A

Maturation
1) remodeling : reorganization, degradation and resynthesis of ECM (collagen III -> collagen I).
Formation of scar tissue.

2) cross-linking : covalent bonds between collagen fibrils.

Result is increases tensile strength (80% of unwounded skin).

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14
Q

How is the healing process different in bone ?

A

Maturation stage is different : soft (fibroblasts, chondroblasts) and hard (osteoblasts) callus formation.

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15
Q

3 wound healing complications

A

1) chronic non-healing wounds (chronic inflammation) : ex diabetic ulcer

2) excessive formation of repair components : hypertrophic scar (collagen I), keloid (collagen III)

3) excessive proliferation of fibroblasts / other connective tissue elements

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16
Q

difference between regenerative medicine and tissue engineering

A

1) boosting the body’s ability to heal -> promote cell growth, but not intiducing new cells

2) if normal healing not possible, take patient’s cells (or allogenic) -> culture -> graft with all cell types and vascularized