Generation of Human-Induced Pluripotent Stem Cells in the Absence of Exogenous Sox2

Author:

Li Wenlin1,Zhou HongYan1,Abujarour Ramzey1,Zhu Saiyong1,Young Joo Jin2,Lin Tongxiang1,Hao Ergeng3,Schöler Hans R.2,Hayek Alberto3,Ding Sheng1

Affiliation:

1. Department of Chemistry, The Scripps Research Institute, La Jolla, California, USA

2. Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany

3. Whittier Institute, Department of Pediatrics, University of California at San Diego, La Jolla, California, USA

Abstract

Abstract Induced pluripotent stem cell technology has attracted enormous interest for potential application in regenerative medicine. Here, we report that a specific glycogen synthase kinase 3 (GSK-3) inhibitor, CHIR99021, can induce the reprogramming of mouse embryonic fibroblasts transduced by only two factors, Oct4 and Klf4. When combined with Parnate (also named tranylcypromine), an inhibitor of lysine-specific demethylase 1, CHIR99021 can cause the reprogramming of human primary keratinocyte transduced with the two factors, Oct4 and Klf4. To our knowledge, this is the first time that human iPS cells have been generated from somatic cells without exogenous Sox2 expression. Our studies suggest that the GSK-3 inhibitor might have a general application to replace transcription factors in both mouse and human reprogramming. Disclosure of potential conflicts of interest is found at the end of this article.

Funder

Fate Therapeutics and CIRM

Larry L Hillblom Foundation

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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