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ChapterIII
TissueRenewalandRepair:RegenerationandFibrosis组织更新与修复:再生和纤维化FibrosisTissuescar
Stimuliremovedsoon(acuteinjury)PersistenttissuedamageIntacttissueframeworkDamagedtissueframeworkSuperficialwoundsSomeinflammatoryprocessesDeepwoundsPerfectreturnofnormalstructure&function
Functionalimperfect
Permanentdysfunction
RegenerationRestitutionofnormalstructureHealingOrganizationofexudateScarformationTissueRenewalandRepairCelldeathPluripotent-cangiverisetoallthetissues.
Regenerativemedicine:stemcellsmayonedaybeusedtorepairinjuryinhumantissues,includingheart,brain,andskeletalmuscle.EmbryonicStemCellsmorerestricteddifferentiationcapacityandusu.lineage-specificAdultStemCellsProlongedself-renewalcapacity+AsymmetricreplicationCellcycleProliferativeCapacityofDifferentCellsLabilecells:
proliferatethroughoutlifeusu.bystemcellssurfacecells;cellsofbonemarrowandhematopoietictissuesRegenerationofsquamouscellsStable(quiescent)cells:normallyhavealowlevelofreplication,butcanundergorapiddivisioninresponsetostimuliandarethuscapableofreconstitutingthetissueoforigin
glandularepitheliaandmesenchymalcellsRegenerationofhepatocytesRegenerationofglandularepithelia
RegenerationofhumanliverCTscansofthedonorliverinlivingdonorhepatictransplantationTheliverofthedonorbeforetheoperation.Therightlobe,whichwillbeusedasatransplant,isoutlined.Oneweekafterperformanceofpartialhepatectomytoremovetherightlobe.Notethegreatenlargementoftheleftlobe(outlined),withoutregrowthoftherightlobe.RegenerationofMesenchyamlcellsRegenerationofChondrocytesRegenerationofosteocytesRegenerationofcapillariesRegenerationofneuralfibersPermanent(nondividing)cells:haveleftthecellcycleandcannotundergomitoticdivisioninpostnatallifeneurons,skeletalandcardiacmusclecellsRegenerationofskeletalmusclecellsCell-cellinteraction
ConditionedmediumContactinhibitionExtracellularmatrix
Laminin:EpitheliaFibroblastsFibronectin:EpitheliaFibroblastsGrowthfactors
EGF,TGF-A,PDGF,aFGF,bFGF,IGF-1,IGF-2,VEGF,HGF,G-CSF,M-CSF,G-CSF,RYTHROPOITIN,ILs,TNF,IFN,NGFRegeneration-factorsinfluencingregenerationHealing
-cutaneouswoundhealingTheprototypeoftissuerepairMediatedthroughGFsandCytokinesDynamic,changingandoverlappingprocessesGrossly:
pink,soft,granularappearanceGranulationTissue-hallmarkofhealingHistologically:Newbloodvessels;Inflammatorycells;FibroblastsGranulationtissueNumerousbloodvessels,edema,andalooseECM,occ.InflammatorycellsTrichomestain:minimalmaturecollegen(blue)MaturescarScatteredvascularchannelsTrichomestain:densecollagen(blue)HealingbyfirstintentionHealingbysecondintentionWoundNarrowsurgicalincisionalspace,cleananduninfectedLargedefects,morenecroticdebrisandexudateInflammationmildmoreintenseRegenerationintactepidermisthinnerepidermisdermalappendageswillbepermanentlylostinbothsituationsGranulationTissuessmallamountabundantRemodelingCharacteristic“woundcontraction”,todecreasethegapbetweentheedgesofthewoundScarformationlittlesubstantialBasedonthenatureofthewound,twotypesofhealingComplicationsinCutaneousWoundHealingDeficientscarformationWounddehiscencebymechanicalstressUlcerationduetoinadequatevasculationExcessivecollagenoftherepaircomponentsAraisedscar:hypertrophicscarScargrowsbeyondtheboundariesoftheoriginalwoundanddoesnotregress:keloid
Exuberantproliferationoffibroblastsandotherconnectivetissueelements,mayrecurafterexcision:desmoidoraggressivefibromatoses,itisalow-gradetumorKeloid:excesscollagendepositionintheskin,formingaraisedscar,andgrowsbeyondtheboundariesoftheoriginalwoundsNormalscarFactorsinfluencingwoundhealingSystemic
NutritionMetabolicstatusCirculatorystatusHormonesLocalInfectionMechanicalfactorsForeignbodiesSize,locationandtypesofwoundAlteredphysiologicstimuliInjuriousstimuliInabilitytoadaptAdaptationMetabolicstimuliDegenerationCellinjuryCelldeathToomuchoverloadedCellularResponsesforKeepingTheir“Homeostasis”AtrophyHypertrophyHyperplasiaMetaplasiaHydropicFatty,
CholesteralHyaline,AmyloidosisLipofuscin,HemosiderinApoptosisNecrosis:Coagulative,Liquefactive,Caseous,Gangrene,Fat,FibrinoidErosion
&Ulcer;Sinus&Fistula;Cavitation&EncapsulationCalcification&PsammomaBodyTissueRenewalandRepai
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