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dc.contributor.authorCassady, John P.
dc.contributor.authorD’Alessio, Ana C.
dc.contributor.authorSarkar, Sovan
dc.contributor.authorFan, Zi Peng
dc.contributor.authorGanz, Kibibi
dc.contributor.authorRoessler, Reinhard
dc.contributor.authorSur, Mriganka
dc.contributor.authorYoung, Richard A.
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorDani, Vardhan
dc.contributor.authorYoung, Richard A.
dc.date.accessioned2015-03-31T15:37:32Z
dc.date.available2015-03-31T15:37:32Z
dc.date.issued2014-11
dc.date.submitted2014-10
dc.identifier.issn22136711
dc.identifier.urihttp://hdl.handle.net/1721.1/96277
dc.description.abstractOverexpression of transcription factors has been used to directly reprogram somatic cells into a range of other differentiated cell types, including multipotent neural stem cells (NSCs), that can be used to generate neurons and glia. However, the ability to maintain the NSC state independent of the inducing factors and the identity of the somatic donor cells remain two important unresolved issues in transdifferentiation. Here we used transduction of doxycycline-inducible transcription factors to generate stable tripotent NSCs. The induced NSCs (iNSCs) maintained their characteristics in the absence of exogenous factor expression and were transcriptionally, epigenetically, and functionally similar to primary brain-derived NSCs. Importantly, we also generated tripotent iNSCs from multiple adult cell types, including mature liver and B cells. Our results show that self-maintaining proliferative neural cells can be induced from nonectodermal cells by expressing specific combinations of transcription factors.en_US
dc.description.sponsorshipHoward Hughes Medical Institute (Gilliam Fellowship)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant HD045022)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R37CA084198)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant HG002668)en_US
dc.description.sponsorshipSimons Foundation (Grant SFARI 204106)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.stemcr.2014.10.001en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/en_US
dc.sourceElsevieren_US
dc.titleDirect Lineage Conversion of Adult Mouse Liver Cells and B Lymphocytes to Neural Stem Cellsen_US
dc.typeArticleen_US
dc.identifier.citationCassady, John P. et al. “Direct Lineage Conversion of Adult Mouse Liver Cells and B Lymphocytes to Neural Stem Cells.” Stem Cell Reports 3.6 (2014): 948–956.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Programen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentPicower Institute for Learning and Memoryen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorDani, Vardhanen_US
dc.contributor.mitauthorFan, Zi Pengen_US
dc.contributor.mitauthorSur, Mrigankaen_US
dc.contributor.mitauthorYoung, Richard A.en_US
dc.contributor.mitauthorCassady, John P.en_US
dc.contributor.mitauthorJaenisch, Rudolfen_US
dc.relation.journalStem Cell Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsCassady, John P.; D’Alessio, Ana C.; Sarkar, Sovan; Dani, Vardhan S.; Fan, Zi Peng; Ganz, Kibibi; Roessler, Reinhard; Sur, Mriganka; Young, Richard A.; Jaenisch, Rudolfen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5478-1568
dc.identifier.orcidhttps://orcid.org/0000-0003-2442-5671
dc.identifier.orcidhttps://orcid.org/0000-0001-8855-8647
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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