Purified Mesenchymal Stem Cells Are an Efficient Source for iPS Cell Induction 英文参考文献.docVIP
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Purified Mesenchymal Stem Cells Are an Efficient Source for iPS Cell Induction 英文参考文献
PurifiedMesenchymalStemCellsAreanEfficientSource
foriPSCellInduction
KunimichiNiibe1,2,YoshimiKawamura1,DaisukeAraki1,2,SatoruMorikawa2,KyokoMiura1 ,Sadafumi
Suzuki1,ShigetoShimmura3,TakehikoSunabori1,YoMabuchi1,YasuoNagai1,TaneakiNakagawa2,
HideyukiOkano1,YumiMatsuzaki1*
1DepartmentofPhysiology,KeioUniversitySchoolofMedicine,Tokyo,Japan,2DepartmentofDentistryandOralSurgery,KeioUniversitySchoolofMedicine,Tokyo,
Japan,3DepartmentofOphthalmology,KeioUniversitySchoolofMedicine,Tokyo,Japan
Abstract
Background: Induced pluripotent stem (iPS) cells are generated from mouse and human somatic cells by the forced
expressionofdefinedtranscriptionfactors.Althoughmostsomaticcellsarecapableofacquiringpluripotencywithminimal
gene transduction, the poor efficiency of cell reprogramming and the uneven quality of iPS cells are still important
problems.Inparticular,thechoiceofcelltypemostsuitableforinducinghigh-qualityiPScellsremainsunclear.
Methodology/PrincipalFindings:Here,wegeneratediPScellsfromPDGFRa+Sca-1+(PaS)adultmousemesenchymalstem
cells (MSCs) and PDGFRa2 Sca-12 osteo-progenitors (OP cells), and compared the induction efficiency and quality of
individualiPSclones.MSCshadahigherreprogrammingefficiencycomparedwithOPcellsandTailTipFibroblasts(TTFs).
The iPS cells induced from MSCs by Oct3/4, Sox2, and Klf4 appeared to be the closest equivalent to ES cells by DNA
microarraygeneprofileandgermline-transmissionefficiency.
Conclusions/Significance: Our findings suggest that a purified source of undifferentiated cells from adult tissue can
produce high-quality iPS cells. In this context, prospectively enriched MSCs are a promising candidate for the efficient
generationofhigh-qualityiPScells.
Citation:NiibeK,KawamuraY,ArakiD,MorikawaS,MiuraK,etal.(2011)PurifiedMesenchymalStemCellsAreanEfficientSourceforiPSCellInduction.PLoS
ONE6(3):e17610.doi:10.1371/journal.pone.0017610
Editor:ElianaAbdelhay,InstitutoNacionaldeCa?ncer, Brazil
ReceivedJanuary6,2011;AcceptedJanuary31,2011;Publis
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