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dc.contributor.authorJiang, Weien_US
dc.contributor.authorZhang, Donghuien_US
dc.contributor.authorBursac, Nenaden_US
dc.contributor.authorZhang, Yien_US
dc.date.accessioned2014-03-10T16:17:37Z
dc.date.issued2013en_US
dc.identifier.citationJiang, Wei, Donghui Zhang, Nenad Bursac, and Yi Zhang. 2013. “WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs.” Stem Cell Reports 1 (1): 46-52. doi:10.1016/j.stemcr.2013.03.003. http://dx.doi.org/10.1016/j.stemcr.2013.03.003.en
dc.identifier.issn2213-6711en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:11877118
dc.description.abstractGeneration of functional cells from human pluripotent stem cells (PSCs) through in vitro differentiation is a promising approach for drug screening and cell therapy. However, the observed large and unavoidable variation in the differentiation potential of different human embryonic stem cell (hESC)/induced PSC (iPSC) lines makes the selection of an appropriate cell line for the differentiation of a particular cell lineage difficult. Here, we report identification of WNT3 as a biomarker capable of predicting definitive endoderm (DE) differentiation potential of hESCs. We show that the mRNA level of WNT3 in hESCs correlates with their DE differentiation efficiency. In addition, manipulations of hESCs through WNT3 knockdown or overexpression can respectively inhibit or promote DE differentiation in a WNT3 level-dependent manner. Finally, analysis of several hESC lines based on their WNT3 expression levels allowed accurate prediction of their DE differentiation potential. Collectively, our study supports the notion that WNT3 can serve as a biomarker for predicting DE differentiation potential of hESCs.en
dc.language.isoen_USen
dc.publisherElsevieren
dc.relation.isversionofdoi:10.1016/j.stemcr.2013.03.003en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757741/pdf/en
dash.licenseLAAen_US
dc.titleWNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCsen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalStem Cell Reportsen
dash.depositing.authorJiang, Weien_US
dc.date.available2014-03-10T16:17:37Z
dc.identifier.doi10.1016/j.stemcr.2013.03.003*
dash.authorsorderedfalse
dash.contributor.affiliatedJiang, Wei
dash.contributor.affiliatedZhang, Yi


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