WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs
Generation 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)/i...
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Elsevier
2013
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757741/ |
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pubmed-37577412013-09-17 WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs Jiang, Wei Zhang, Donghui Bursac, Nenad Zhang, Yi Report Generation 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. Elsevier 2013-06-04 /pmc/articles/PMC3757741/ /pubmed/24052941 http://dx.doi.org/10.1016/j.stemcr.2013.03.003 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Jiang, Wei Zhang, Donghui Bursac, Nenad Zhang, Yi |
spellingShingle |
Jiang, Wei Zhang, Donghui Bursac, Nenad Zhang, Yi WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs |
author_facet |
Jiang, Wei Zhang, Donghui Bursac, Nenad Zhang, Yi |
author_sort |
Jiang, Wei |
title |
WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs |
title_short |
WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs |
title_full |
WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs |
title_fullStr |
WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs |
title_full_unstemmed |
WNT3 Is a Biomarker Capable of Predicting the Definitive Endoderm Differentiation Potential of hESCs |
title_sort |
wnt3 is a biomarker capable of predicting the definitive endoderm differentiation potential of hescs |
description |
Generation 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. |
publisher |
Elsevier |
publishDate |
2013 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757741/ |
_version_ |
1612007079781859328 |