chapter 3 te
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ssue ynam cs
Chapter 3
Patricia Relue
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Tissue replacement ratesa e .
Bone marrowmakes as many
every 2-3 days
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Difference between rate andcharacteristic time
, Rate or reaction rate, units of time-1
Reaction rate and characteristic time areinversely related Short characteristic time, fast rate
Exam le: ex onential deca . The half-lifeis the characteristic time for the process.If the rate of decay increases, the half-lifedecreases.
Example: growth rate of cells and the celldoubling time
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ynam c states o t ssue
Normal steady state function of tissue Cell production (bone marrow), transport
, ,
Tissue repair
Healing response due to wound
Tissue formation (Chapter 4) Developmental biology and morphogenesis
ounger ssues possess more organogen cpotential Stem cells
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one marrow an ematopo es s
Most rapidly replacing tissue, every2-3 days
400 billion cells/day produced
Most cells produced are highlyi erentiate an s ort- ive
T cell, B cell, erythrocyte,
neutrop , monocyte(macrophage), eosinophil, basophil,
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Villi in the smallntest ne g .
e pro uc on
occurs in the crypt
Differentiate as theymove up the crypt
Mature cells leavethe crypt
Function in theabsorption ofnutrients for ut
lumen; cell turnoverevery ~5 days, dieand slou h off
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n gure .
Basal layer hasType VII co agen
1 in 10-12 basalcells is
progenitor ce Turnover is a few
weeks
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oun ea ng v eo
http://www.youtube.com/watch?v=zZpMQ_7qiRg
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Wound healing in adult skingure .
Control of bleeding starts with rapid adhesion Agents released by platelets now Inflammatory cells Granulation tissue has
of circulating platelets to site of damage
Activated platelets secrete contents of storagegranules, spread, recruit more platelets
cause vaso a on an ncrease oo
vessel permeability Clotting cascade initiated, fibrinogencleaved by thrombin to form fibrin
m gra e o e n ury
Neutrophils begin todegranulate and die Macrophages arrive
orme ense ro as s,
macrophages, and developingvasculature)Matrix is mainly fibronectin,
Hemorrhaging is contained by blood vesselconstriction
Hemostasis Thrombosis Inflammation Granulation tissue/
p ug Fibrin plug + fibronectin holds tissuetogether and forms provisional matrix
Matrix recruits inflammatory cells
rom c rcu a on Macrophagessecrete compounds
to attract endothelial
co agen , an ya uron cacid Collagen increases the tensile
strength of the wound neovascularizationan a er ro as s an o er ce s
Epidermal cells proliferate andmigrate across the wound
ce s an ro as s,stimulate proliferation Basal layer reformsin epidermal layer
yo ro as s con rac ,pulling wound marginstogether Epidermis has stratified
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tages o woun repa r
emos as s
Thrombosis
ranu a ontissue/neovascularization
Wound appears healed
Matrix is s nthesized de raded
Collagen type III replaced by type I
Processes determine scar formation
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art age repa r gure .4
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Placement of reconstituted tissues in vivo
induces responses similar to wound healing
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ng neere woun ea ng
quare, u c ness woun ma e n s n
Porous ECM template inserted into wound Com osed of colla en I and chondroitin-6-
sulfates
Variable pore size
Variable de radation rates
Templates were tested for ability to delaywound contracture and promote dermal
Time required for the wound area todecrease by 50% was measured
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Effect of porous template onwoun ea ng gure .5
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Optimal range of pore diameter
(maximum wound healing delay)
Degradation rate was found
optimal when tuned to normalhealing rate, td ts
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Effect of pore size and degradation onwound healing rate
s oug a e e ay n woun
healing is related to improved healingcorrelates to fibroblast migration
Wound contracture normally occurs afterfibroblasts span the provisional matrix
Small pore sizes (120 m Area per volume for cell adhesion is small
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Contraction of cell-laden matricesgure .6
Exam le ofin vitrowound healing response
Cells apply tension to theECM
Tension resu ts in matrixcontraction
Circular matricesdiameter by action ofcells on matrix (diameterdecreases)
cell-matrix contraction Ability of cells to remodel
and contract matrix is
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used to engineer tissuein vitro
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Aspects of fetal and adult woundea ng responses a e .
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Insight into fetal wound healing can provide stategies for improvingadult wound healing and integration of TEMPs into the body
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Tissue dynamics as interacting cellularfate processes (Figure 3.7)
Pathology
Means for cells tocommunicate and
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coordinate their
efforts
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uest ons
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