Self-renewal of embryonic stem cells by a small molecule

被引:238
作者
Chen, Shuibing
Do, Jeong Tae
Zhang, Qisheng
Yao, Shuyuan
Yan, Feng
Peters, Eric C.
Schoeler, Hans R.
Schultz, Peter G.
Ding, Sheng
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3] Max Planck Inst Mol Biomed, Dept Cell & Dev Biol, D-48149 Munster, Germany
[4] Novartis Res Fdn, Genom Inst, San Diego, CA 92121 USA
关键词
pluripotency; cell-based screen; SC1; ERK1; Ras GTPase-activating protein;
D O I
10.1073/pnas.0608156103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
A cell-based screen of chemical libraries was carried out to identify small molecules that control the self-renewal of ES cells. A previously uncharacterized heterocycle, SC1, was discovered that allows one to propagate murine ES cells in an undifferentiated, pluripotent state under chemically defined conditions in the absence of feeder cells, serum, and leukemia inhibitory factor. Long-term SC1-expanded murine ES cells can be differentiated into cells of the three primary germ layers in vitro and also can generate chimeric mice and contribute to the germ line in vivo. Biochemical and cellular experiments suggest that SC1 works through dual inhibition of RasGAP and ERK1. Molecules of this kind may not only facilitate practical applications of stem cells in research and therapy, but also provide previously undescribed insights into the complex biology of stem cells.
引用
收藏
页码:17266 / 17271
页数:6
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