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dc.contributor.authorForster, Ryan
dc.contributor.authorChiba, Kunitoshi
dc.contributor.authorSchaeffer, Lorian
dc.contributor.authorRegalado, Samuel G.
dc.contributor.authorLai, Christine S.
dc.contributor.authorGao, Qing
dc.contributor.authorKiani, Samira
dc.contributor.authorFarin, Henner F.
dc.contributor.authorClevers, Hans
dc.contributor.authorCost, Gregory J.
dc.contributor.authorChan, Andy
dc.contributor.authorRebar, Edward J.
dc.contributor.authorUrnov, Fyodor D.
dc.contributor.authorGregory, Philip D.
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorHockemeyer, Dirk
dc.contributor.authorPachter, Lior, 1973-
dc.date.accessioned2015-03-31T16:25:47Z
dc.date.available2015-03-31T16:25:47Z
dc.date.issued2014-06
dc.date.submitted2014-05
dc.identifier.issn22136711
dc.identifier.urihttp://hdl.handle.net/1721.1/96280
dc.description.abstractGenetically engineered human pluripotent stem cells (hPSCs) have been proposed as a source for transplantation therapies and are rapidly becoming valuable tools for human disease modeling. However, many applications are limited due to the lack of robust differentiation paradigms that allow for the isolation of defined functional tissues. Here, using an endogenous LGR5-GFP reporter, we derived adult stem cells from hPSCs that gave rise to functional human intestinal tissue comprising all major cell types of the intestine. Histological and functional analyses revealed that such human organoid cultures could be derived with high purity and with a composition and morphology similar to those of cultures obtained from human biopsies. Importantly, hPSC-derived organoids responded to the canonical signaling pathways that control self-renewal and differentiation in the adult human intestinal stem cell compartment. This adult stem cell system provides a platform for studying human intestinal disease in vitro using genetically engineered hPSCs.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R37-CA084198)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). (Grant RO1-CA087869)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant RO1-HD045022)en_US
dc.description.sponsorshipHoward Hughes Medical Institute (Grant)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.stemcr.2014.05.001en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/en_US
dc.sourceElsevieren_US
dc.titleHuman Intestinal Tissue with Adult Stem Cell Properties Derived from Pluripotent Stem Cellsen_US
dc.typeArticleen_US
dc.identifier.citationForster, Ryan, Kunitoshi Chiba, Lorian Schaeffer, Samuel G. Regalado, Christine S. Lai, Qing Gao, Samira Kiani, et al. “Human Intestinal Tissue with Adult Stem Cell Properties Derived from Pluripotent Stem Cells.” Stem Cell Reports 2, no. 6 (June 2014): 838–852.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorJaenisch, Rudolfen_US
dc.contributor.mitauthorKiani, Samiraen_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.orderedauthorsForster, Ryan; Chiba, Kunitoshi; Schaeffer, Lorian; Regalado, Samuel G.; Lai, Christine S.; Gao, Qing; Kiani, Samira; Farin, Henner F.; Clevers, Hans; Cost, Gregory J.; Chan, Andy; Rebar, Edward J.; Urnov, Fyodor D.; Gregory, Philip D.; Pachter, Lior; Jaenisch, Rudolf; Hockemeyer, Dirken_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1736-0937
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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