ARTICLEINPRESS
ActaBiomaterialiaxxx(2007)
xxx–xxx
Briefcommunication
Celladhesionandmechanicalpropertiesofa exiblesca oldfor
cardiactissueengineering
L.A.Hidalgo-Bastidaa,J.J.A.Barrya,N.M.Everittb,F.R.A.J.Rosea,L.D.Butterya,
I.P.Hallc,W.C.Claycombd,K.M.Shakeshe a,*
c
DivisionofDrugDeliveryandTissueEngineering,SchoolofPharmacy,UniversityofNottingham,NottinghamNG72RD,UK
Bioengineering,SchoolofMechanical,MaterialsandManufacturingEngineering,UniversityofNottingham,NottinghamNG72RD,UK
DivisionofTherapeuticsandMolecularMedicine,SchoolofMedicalandSurgicalSciences,UniversityHospitalNottingham,NottinghamNG72UH,UK
d
BiochemistryandMolecularBiology,SchoolofMedicineatNewOrleans,LouisianaStateUniversity,BatonRouge,LA,USA
b
a
Received21March2006;receivedinrevisedform7December2006;accepted12December2006
Abstract
Cardiactissueengineeringisfocusedonobtainingfunctionalcardiomyocyteconstructstoprovideanalternativetocellularcardio-myoplasty.Mechanicalstimulihavebeenshowntostimulateproteinexpressionandthedi erentiationofmammaliancellsfromcon-tractiletissues.Ouraimwastoobtaina exiblesca oldwhichcouldbeusedtoapplymechanicalforcesduringtissueregeneration.Poly(1,8-octanediol-co-citricacid)(POC)isanelastomerthatcanbeprocessedintosca oldsfortissueengineering.Weinvestigatedthee ectofmodifyingtheporosityonthemechanicalpropertiesofthePOCsca olds.Inaddition,thee ectsofthestoragemethodandstrainrateonmaterialintegritywereassessed.ThemaximumelongationofPOCporous lmsvariedfrom60%to160%oftheiroriginallength.Adecreaseintheporositycausedariseinthiselasticmodulus.TheattachmentofHL-1cardiomyocytestoPOCwasassessedon lmscoatedwith bronectin,collagenandlaminin.Theseextracellularmatrixproteinspromotedcelladhesioninapro-tein-type-andconcentration-dependentmanner.Therefore,POCsca oldscanbeoptimisedtomeetthemechanicalandbiologicalparametersneededforcardiacculture.Thisporousmaterialhasthepotentialtobeusedforcardiactissueengineeringaswellasforothersofttissueapplications.
Ó2007ActaMaterialiaInc.PublishedbyElsevierLtd.Allrightsreserved.
Keywords:Sca old;Poly(1,8-octanediol-co-citricacid)(POC);Elastomer;Cardiomyocyte;Tissueengineering
1.Introduction
CardiovasculardiseaseshavebecomethemaincauseofdeathnotonlyinWesterncountriesbutalsoinmanydevel-opingnations[1].Currenttherapiesforcardiacfailure(withtheexceptionofcardiactransplantation)ingeneralprovidelimitedimprovementsincardiacoutputandrelatedsymp-toms.Cardiactransplantation,thebesttherapyavailable,isrestrictedbytheshortageofdonorsandtheriskoftissuerejection.Recentresearchhasconcentratedonnewalterna-tives,suchascardiaccellularmyoplasty,whichcould
Correspondingauthor.Tel.:+441159515104.
E-mailaddress:kevin.shakeshe @nottingham.ac.uk(K.M.Shake-
she ).
*potentiallyimproveoutcomesintermsofbothmorbidityandmortality[2].Apotentialalternativetreatmentcouldbeachievedbyusingaphysicalsupportcontaininggrowthfactorscapableofinducingspeci ccellulardi erentiationtogenerateanengineeredcardiacconstruct.Aninitialchal-lengeofgeneratinganengineeredcardiacpatchisthedevel-opmentoftheidealbiomaterialforcardiomyocyteculture.Researchershaveproposedbothsyntheticandnaturalmaterialstogenerateasuitablecardiacgraft.Naturalpoly-merssuchascollagenwere rstusedforcardiacsca olds,buttheyexhibitedlimitedmechanicalpropertiesandbatch-to-batchvariation[3].RadisicandVunjak-Novako-vicstatedthatcollagenisnotacandidateforcardiacscaf-foldsbecauseofits‘‘poorstructuralintegrity’’[4].Syntheticpolymershavealsobeeninvestigated;Bursac
1742-7061/$-seefrontmatterÓ2007ActaMaterialiaInc.PublishedbyElsevierLtd.Allrightsreserved.doi:10.1016/j.actbio.2006.12.006
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