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36 Cards in this Set

  • Front
  • Back
Regeneration
a. Complete regeneration of lost tissue
b. Requires intact ECM
c. Seen in tissues with high proliferative activity
Repair
a. Combination of regeneration and scar formation by collagen deposition
b. Dominant process where ECM is damaged
c. Partial or complete restoration of function (usually partial)
Liver regeneration
a. Requires an intact extracellular matrix
Liver repair by scarring
a. Matrix is damaged
b. Injury is repaired by fibrous tissue deposition and scar formation
Continuously dividing cells
i. Labile
ii. Proliferate throughout life
iii. Bone marrow, epidermis
Quiescent cells
i. Stable
ii. Normally involved in low-level replication
iii. May not respond to stimuli by rapid division
iv. Liver, fibroblasts, kidney, smooth mucle
Non-dividing cells
i. Permanent
ii. Do not undergo division in post-natal life
iii. Neurons, cardiac myocytes
Pluripotent embryonic stem cells
1. Capacity for self renewal
2. Capacity to generate all cell lineages
3. Give rise to multipotent stem cells
Multipotent stem cells
1. More restricted development potential
2. Eventually produce differentiated cells
Somatic stem cells
i. Identified in many mature tissues (bone marrow, skin, GI, liver, pancreas and fat)
ii. More limited capacity to differentiate
iii. Give rise to rapidly proliferating cells that become progenitor cells which have more limited developmental potential
Niche
1. Somatic cell microenvironment
2. Composed of mesenchyman, endothelial, and other cell types
Niche cells
1. Generate or transmit stimuli that regulate stem cell self-renewal and the generation of progeny cells
Transdifferentiation
1. Cells differentiate from one type to another
2. “Developmental plasticity”
3. Mature cells do not do this
4. Hematopoietic stem cells may be induced to differentiate into other cell types
Repair and wound healing ECM/cell matrix
1. ECM regulates growth, proliferation, movement and differentiation of cells living within it
2. Constantly remodeling
3. Integral to morphogenesis, regeneration, wound healing, chronic fibrotic processes, tumor invasion and metastasis
4. Sequesters water, provides turgor to soft tissues and minerals for bone
ECM functions
1. Provides mechanical support and structure
2. Controls cell growth
3. Maintains cell differentiation
4. Provides scaffolding for tissue renewal
5. Establishes specialized microenvironments for various tissues
6. Provides storage and presentation of regulatory molecules
Collagens
Tensile strength
Elastins
Recoil
Adhesive glycoproteins
1. Connect components to one another and to cells
2. Mostly transmembrane receptors
3. Ig family, integrins, selectins, cadherins
Proteoglycans and glycosaminoglycans
1. Resilience and lubrication
Healing by repair, scar formation, and fibrosis
i. Tissue injury resulting in damage of parenchyma and stromal elements cannot heal by regeneration, but instead by repair and scarring
Healing by repair, scar formation and fibrosis is affected by....
1. Proliferative capacity of damaged tissue
2. Integrity of ECM
3. Degree and chronicity of inflammation
Sequence of healing
a. Inflammation
b. Angiogenesis
c. Migration and proliferation of fibroblasts
d. Scar formation
e. Connective tissue remodeling
Clot formation
a. Wounding causes activation of platelets and coagulation pathways resulting in blood clot
b. Stops bleeding and acts as scaffold for cells attracted to area by chemokines, cytokines, and growth factors
c. Within 24 hours, neutrophils appear, use scaffolding to move in and clean up mess
Granulation tissue formation
a. Proliferation of fibroblasts and vascular endothelium starts in 1-3 days
b. Peaks around 5-7 days
c. Forms a framework for scar formation
Characteristic histologic features of granulation tissue formation
i. Small new blood vessels due to angiogenesis
ii. Proliferation of fibroblasts
iii. Vessels are leaky→ tissue is edematous
Neutrophils
i. Largely replaced by macrophages by 2-4 days
Macrophages
i. Clear extracellular debris, fibrin, foreign material
ii. Promote angiogenesis and ECM deposition
iii. Main source of many growth factors in healing wounds that drive fibroblast migration, proliferation, and ECM production
Re-epithelialization
i. 2-4 days, well underway
ii. Takes much longer to fill in larger wounds
Scar formation
a. By 2nd week, leukocytes and granulation tissue have mainly disappeared
b. Blanching begins with increased collagen around wound area
c. Regression of vascular channels
d. Dermal appendages are lost
e. End of 1st month, scar composed of acellular connective tissue w/o inflammation, covered by intact epidermis
Granulation tissue conversion
i. Avascular scar composed of→
ii. Fibroblasts, collagen, fragments of elastic tissue, other ECM components
Wound contraction
a. Generally occurs in large wounds (2nd intention)
b. Myofibroblasts contract in wound tissue
c. Helps close gap by decreasing the distance between the dermal edges and reducing wound surface area
Characteristics of healing by 2nd intention vs. primary intention
a. More debris to remove
b. More intense inflammation
c. Larger amounts of granulation tissue are formed
d. Edges of wound on surface do not join
e. During the scarring process, the wound contracts
Keloid
a. Excess collagen deposition in the skin
b. Raised scar
Wound dehiscence
a. Inadequate formation of granulation tissue or assembly of a scar
b. Can also lead to ulceration
c. Most common after abdominal surgery
Ulceration
a. Wounds can ulcerate because of inadequate vascularization during healing
Fibromatoses
a. Lie in interface between benign proliferations and malignant tumors