Induction of Pluripotent Stem Cells from Mouse Emb.docx
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Induction of Pluripotent Stem Cells from Mouse Emb.docx
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InductionofPluripotentStemCellsfromMouseEmb
InductionofPluripotentStemCellsfromMouseEmbryonicandAdultFibroblastCulturesbyDefinedFactors
SUMMARY
Differentiatedcellscanbereprogrammedtoanembryonic-likestatebytransferofnuclearcontentsintooocytesorbyfusionwithembryonicstem(ES)cells.Littleisknownaboutfactorsthatinducethisreprogramming.Here,wedemonstrateinductionofpluripotentstemcellsfrommouseembryonicoradultfibroblastsbyintroducingfourfactors,Oct3/4,Sox2,c-Myc,andKlf4,underEScellcultureconditions.Unexpectedly,Nanogwasdispensable.Thesecells,whichwedesignatediPS(inducedpluripotentstem)cells,exhibitthemorphologyandgrowthpropertiesofEScellsandexpressEScellmarkergenes.SubcutaneoustransplantationofiPScellsintonudemiceresultedintumorscontainingavarietyoftissuesfromallthreegermlayers.Followinginjectionintoblastocysts,iPScellscontributedtomouseembryonicdevelopment.Thesedatademonstratethatpluripotentstemcellscanbedirectlygeneratedfromfibroblastculturesbytheadditionofonlyafewdefinedfactors.
INTRODUCTION
Embryonicstem(ES)cells,whicharederivedfromtheinnercellmassofmammalianblastocysts,havetheabilitytogrowindefinitelywhilemaintainingpluripotencyandtheabilitytodifferentiateintocellsofallthreegermlayers(EvansandKaufman,1981;Martin,1981).HumanEScellsmightbeusedtotreatahostofdiseases,suchasParkinson’sdisease,spinalcordinjury,anddiabetes(Thomsonetal.,1998).However,thereareethicaldifficultiesregardingtheuseofhumanembryos,aswellastheproblemoftissuerejectionfollowingtransplantationinpatients.Onewaytocircumventtheseissuesisthegenerationofpluripotentcellsdirectlyfromthepatients’owncells.
Somaticcellscanbereprogrammedbytransferringtheirnuclearcontentsintooocytes(Wilmutetal.,1997)orbyfusionwithEScells(Cowanetal.,2005;Tadaetal.,2001),indicatingthatunfertilizedeggsandEScellscontainfactorsthatcanconfertotipotencyorpluripotencytosomaticcells.WehypothesizedthatthefactorsthatplayimportantrolesinthemaintenanceofEScellidentityalsoplaypivotalrolesintheinductionofpluripotencyinsomaticcells.
Severaltranscriptionfactors,includingOct3/4(Nicholsetal.,1998;Niwaetal.,2000),Sox2(Avilionetal.,2003),andNanog(Chambersetal.,2003;Mitsuietal.,2003),functioninthemaintenanceofpluripotencyinbothearlyembryosandEScells.Severalgenesthatarefrequentlyupregulatedintumors,suchasStat3(Matsudaetal.,1999;Niwaetal.,1998),E-Ras(Takahashietal.,2003),c-myc(Cartwrightetal.,2005),Klf4(Lietal.,2005),andb-catenin(Kielmanetal.,2002;Satoetal.,2004),havebeenshowntocontributetothelong-termmaintenanceoftheEScellphenotypeandtherapidproliferationofEScellsinculture.Inaddition,wehaveidentifiedseveralothergenesthatarespecificallyexpressedinEScells(Maruyamaetal.,2005;Mitsuietal.,2003).
Inthisstudy,weexaminedwhetherthesefactorscouldinducepluripotencyinsomaticcells.Bycombiningfourselectedfactors,wewereabletogeneratepluripotentcells,whichwecallinducedpluripotentstem(iPS)cells,directlyfrommouseembryonicoradultfibroblastcultures.
RESULTS
Weselected24genesascandidatesforfactorsthatinducepluripotencyinsomaticcells,basedonourhypothesisthatsuchfactorsalsoplaypivotalrolesinthemaintenanceofEScellidentity(seeTableS1intheSupplementalDataavailablewiththisarticleonline).Forb-catenin,c-Myc,andStat3,weusedactiveforms,S33Y-b-catenin(Sadotetal.,2002),T58A-c-Myc(Changetal.,2000),andStat3-C(Brombergetal.,1999),respectively.BecauseofthereportednegativeeffectofGrb2onpluripotency(Burdonetal.,1999;Chengetal.,1998),weincludeditsdominant-negativemutantGrb2DSH2(Miyamotoetal.,2004)as1ofthe24candidates.
Figure1.GenerationofiPSCellsfromMEFCulturesvia24Factors
(A)Strategytotestcandidatefactors.
(B)G418-resistantcolonieswereobserved16daysaftertransductionwithacombinationof24factors.Cellswerestainedwithcrystalviolet.
(C)MorphologyofEScells,iPScells(iPS-MEF24,clone1-9),andMEFs.Scalebars=200mm.(D)GrowthcurvesofEScells,iPScells(iPS-MEF24,clones2-1–4),andMEFs.33105cellswerepassagedevery3daysintoeachwellofsix-wellplates.
(E)RT-PCRanalysisofEScellmarkergenesiniPScells(iPS-MEF24,clones1-5,1-9,and1-18),EScells,andMEFs.Nat1wasusedasaloadingcontrol.
(F)BisulfitegenomicsequencingofthepromoterregionsofOct3/4,Nanog,andFbx15iniPScells(iPS-MEF24,clones1-5,1-9,and1-18),EScells,andMEFs.OpencirclesindicateunmethylatedCpGdinucleotides,whileclosedcirclesi
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