Systematic Identification of Culture Conditions for Induction and Maintenance of Naive Human Pluripotency (vol 15, pg 471, 2014)

被引:65
|
作者
Theunissen, Thorold W.
Powell, Benjamin E.
Wang, Haoyi
Mitalipova, Maya
Faddah, Dina A.
Reddy, Jessica
Fan, Zi Peng
Maetzel, Dorothea
Ganz, Kibibi
Shi, Linyu
Lungjangwa, Tenzin
Imsoonthornruksa, Sumeth
Stelzer, Yonatan
Rangarajan, Sudharshan
D'Alessio, Ana
Zhang, Jianming
Gao, Qing
Dawlaty, Meelad M.
Young, Richard A.
Gray, Nathanael S.
Jaenisch, Rudolf
机构
[1] Whitehead Institute for Biomedical Research, Cambridge
[2] Department of Biology, Massachusetts Institute of Technology, Cambridge
[3] Computational and Systems Biology Program, Massachusetts Institute of Technology, Cambridge
[4] Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston
基金
美国国家科学基金会; 英国惠康基金;
关键词
D O I
10.1016/j.stem.2014.09.003
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Embryonic stem cells (ESCs) of mice and humans have distinct molecular and biological characteristics, raising the question of whether an earlier, "naive" state of pluripotency may exist in humans. Here we took a systematic approach to identify small molecules that support self-renewal of naive human ESCs based on maintenance of endogenous OCT4 distal enhancer activity, a molecular signature of ground state pluripotency. Iterative chemical screening identified a combination of five kinase inhibitors that induces and maintains OCT4 distal enhancer activity when applied directly to conventional human ESCs. These inhibitors generate human pluripotent cells in which transcription factors associated with the ground state of pluripotency are highly upregulated and bivalent chromatin domains are depleted. Comparison with previously reported naive human ESCs indicates that our conditions capture a distinct pluripotent state in humans that closely resembles that of mouse ESCs. This study presents a framework for defining the culture requirements of naive human pluripotent cells.
引用
收藏
页码:524 / 526
页数:3
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