Repair and Healing Flashcards
possible outcomes of acute inflammation
- resolution (back to NORMAL fxn)
- progression to chronic inflammation
- healing to fibrosis (LOSS of function; activation of fibroblasts)
outcome of chronic inflammation
ALWAYS fibrosis (loss of function)
regeneration
replacement of damaged tissue with native tissue
*driven by growth factors
regeneration & labile tissues
*tissues in which cells are continuously lost and replaced by maturation from stem cells and by proliferation of mature cells
*CONTINUOUSLY DIVIDING CELLS (good at regeneration)
*skin, small/large bowel, bone marrow
regeneration & stable tissues
*quiescent cells (G0) that can re-enter the cell cycle to regenerate cells if necessary
*minimal proliferative activity in normal state but can be induced to regenerate
*liver & kidney parenchyma, blood vessels, smooth muscle cells
regeneration & permanent tissues
*LACK regenerative potential
*REPAIR replaces damaged tissue with a FIBROUS SCAR
*myocardium, neurons, skeletal muscle
repair
replacement of damaged tissue with a fibrous scar
*always involves inflammation
5 steps of repair by scar
- inflammation
- angiogenesis
- migration and proliferation of fibroblasts
- scar formation
- connective tissue remodeling
repair by scar: 1) inflammation
*MACROPHAGES play a central role
-clear debris, dead tissue, and pathogens
-provide antimicrobial activity
-provide growth factors
-secrete cytokines
repair by scar: 2) angiogenesis
*new blood vessel development from existing vessels
*critical in healing (need oxygen and nutrients; need to remove wastes)
*induced by macrophages
repair by scar: 3) formation of granulation tissue
*migration and proliferation of fibroblasts, blood vessels, and deposition of loose connective tissue
*pink, soft, granular appearance (e.g. beneath the scab of a wound)
*fibroblasts make collagen 3
repair by scar: 4) deposition of connective tissue
*deposition of ECM proteins produced by fibroblasts (replacing collagen 3 with collagen 1)
repair by scar: 5) remodeling of connective tissue
*maturation and reorganization of the connective tissue to produce the stable fibrous scar
*myofibroblasts contract the scar (pull it tighter)
healing by first intention
*only a FOCAL DISRUPTION (e.g. incisions) of epithelial basement membrane and death of relatively few epithelial and connective tissue cells
3 processes of healing by first intention
- inflammation
- cell proliferation
- connective tissue maturation & scar
healing by second intention
*when cell or tissue loss is more extensive (eg. large, ulcerative processes)
*healing from the base up to the surface
processes of healing by second intention
*combination of regeneration and scarring
1. inflammation
2. development of granulation tissue
3. accumulation of ECM and formation of large scar
4. wound contraction by myofibroblasts
parenchymal (visceral) repair by scar
*basic mechanisms are the same as skin repair
*could lead to fibrosis (excess collagen deposition) that leads to loss of function
local issues that can cause delayed healing
*infection
*extent/size/type of injury
*mechanical factors (pressure, torsion)
*foreign bodies (sutures, etc)
*location of wound
systemic issues that can cause delayed healing
*nutrition (vitamin or cofactor deficiencies)
*metabolic status (diabetes)
*circulatory status (atherosclerosis)
*hormones/steroids (anti-inflammatory effects)
dehiscence (pathologic tissue repair)
*rupture of wounds due to insufficient collagen deposition
*ex. abdominal wounds - due to increased abdominal pressure or mechanical stress on the wound
ulceration (pathologic tissue repair)
*inadequate vascularization
*common in lower extremity wounds in people with atherosclerosis
hypertrophic scar (pathologic tissue repair)
excessive collagen confined to wound (localized, raised scar)
keloid (pathologic tissue repair)
scar tissue grows beyond boundaries of original wound (collagen type 3)
exuberant granulation tissue (pathologic tissue repair)
*protrudes above the level of the surrounding skin re-epithelialization (due to too much vascular supply)
*“pyogenic granuloma”