Stress-mediated p38 activation promotes somatic cell reprogramming

被引:33
|
作者
Xu, Xinxiu [1 ,2 ]
Wang, Quan [2 ]
Long, Yuan [2 ]
Zhang, Ru [1 ]
Wei, Xiaoyuan [1 ]
Xing, Mingzhe [1 ]
Gu, Haifeng [2 ]
Xie, Xin [1 ,2 ]
机构
[1] Tongji Univ, Lab Receptor Based Biomed, Shanghai Key Lab Signaling & Dis Res, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, Natl Ctr Drug Screening, Stake Key Lab Drug Res, Shanghai 201203, Peoples R China
关键词
induced pluripotent stem cells; iPS; hyperosmosis; NaCl; stress; p38; reprogramming; PLURIPOTENT STEM-CELLS; GENE-EXPRESSION; FIBROBLASTS; DIFFERENTIATION; GENERATION; INDUCTION;
D O I
10.1038/cr.2012.143
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Environmental stress-mediated adaptation plays essential roles in the evolution of life. Cellular adaptation mechanisms usually involve the regulation of chromatin structure, transcription, mRNA stability and translation, which eventually lead to efficient changes in gene expression. Global epigenetic change is also involved in the reprogramming of somatic cells into induced pluripotent stem (iPS) cells by defined factors. Here we report that environmental stress such as hyperosmosis not only facilitates four factor-mediated reprogramming, but also enhances two or one factor-induced iPS cell generation. Hyperosmosis-induced p38 activation plays a critical role in this process. Constitutive active p38 mimics the positive effect of hyperosmosis, while dominant negative p38 and p38 inhibitor block the effect of hyperosmosis. Further study indicates stress-mediated p38 activation may promote reprogramming by reducing the global DNA methylation level and enhancing the expression of pluripotency genes. Our results demonstrate how simple environmental stress like hyperosmosis helps to alter the fate of cells via intracellular signaling and epigenetic modulation.
引用
收藏
页码:131 / 141
页数:11
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