Single cell transcriptional profiling reveals heterogeneity of human induced pluripotent stem cells

Kazim Narsinh(Stanford University), Ning Sun(Stanford University), Verónica Sánchez-Freire(Stanford University), Andrew S. Lee(Stanford University), Patricia E. de Almeida(Stanford University), Shijun Hu(Stanford University), Taha A. Jan(Institute for Stem Cell Biology and Regenerative Medicine), Kitchener D. Wilson(Stanford University), Denise E. Leong, Jarrett Rosenberg(Stanford University), Mylene Yao, Robert C. Robbins(Stanford University), Joseph C. Wu(Institute for Stem Cell Biology and Regenerative Medicine)
Journal of Clinical Investigation
February 16, 2011
Cited by 277Open Access
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Abstract

Human induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs) are promising candidate cell sources for regenerative medicine. However, despite the common ability of hiPSCs and hESCs to differentiate into all 3 germ layers, their functional equivalence at the single cell level remains to be demonstrated. Moreover, single cell heterogeneity amongst stem cell populations may underlie important cell fate decisions. Here, we used single cell analysis to resolve the gene expression profiles of 362 hiPSCs and hESCs for an array of 42 genes that characterize the pluripotent and differentiated states. Comparison between single hESCs and single hiPSCs revealed markedly more heterogeneity in gene expression levels in the hiPSCs, suggesting that hiPSCs occupy an alternate, less stable pluripotent state. hiPSCs also displayed slower growth kinetics and impaired directed differentiation as compared with hESCs. Our results suggest that caution should be exercised before assuming that hiPSCs occupy a pluripotent state equivalent to that of hESCs, particularly when producing differentiated cells for regenerative medicine aims.


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