Caspase activity mediates the differentiation of embryonic stem cells

被引:235
作者
Fujita, Jun [1 ]
Crane, Ana M. [1 ]
Souza, Marion K. [1 ]
Dejosez, Marion [1 ]
Kyba, Michael [4 ]
Flavell, Richard A. [5 ,6 ]
Thomson, James A. [7 ]
Zwaka, Thomas P. [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Dev Biol, Dallas, TX 75390 USA
[5] Yale Univ, Dept Immunobiol, Sch Med, New Haven, CT 06520 USA
[6] Howard Hughes Med Inst, New Haven, CT 06520 USA
[7] Univ Wisconsin, Wisconsin Natl Primate Res Ctr, Madison, WI 53715 USA
关键词
D O I
10.1016/j.stem.2008.04.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Embryonic stem cells (ESCs) are capable of indefinite self-renewal while retaining the ability to differentiate to any of the three germ layers that give rise to all somatic cell types. An emerging view is that a core set of transcription factors, including Oct4, Sox2, and Nanog, form a robust autoregulatory circuit that maintains ESCs in a self-renewing state. To accommodate the capacity of such cells to undergo germ layer-specific differentiation, we predicted a posttranslational mechanism that could negatively regulate these core self-renewal factors. Here we report caspase-induced cleavage of Nanog in differentiating ESCs. Stem cells lacking the Casp3 gene showed marked defects in differentiation, while forced expression of a caspase cleavage-resistant Nanog mutant in ESCs strongly promoted self-renewal. These results link a major component of the programmed cell-death pathway to the regulation of ESC development.
引用
收藏
页码:595 / 601
页数:7
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