Ding Sheng, Wu Tom Y H, Brinker Achim, Peters Eric C, Hur Wooyoung, Gray Nathanael S, Schultz Peter G
Department of Chemistry and the Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7632-7. doi: 10.1073/pnas.0732087100. Epub 2003 Jun 6.
In an attempt to better understand and control the processes that regulate stem cell fate, we have set out to identify small molecules that induce neuronal differentiation in embryonic stem cells (ESCs). A high-throughput phenotypic cell-based screen of kinase-directed combinatorial libraries led to the discovery of TWS119, a 4,6-disubstituted pyrrolopyrimidine that can induce neurogenesis in murine ESCs. The target of TWS119 was shown to be glycogen synthase kinase-3beta (GSK-3beta) by both affinity-based and biochemical methods. This study provides evidence that GSK-3beta is involved in the induction of mammalian neurogenesis in ESCs. This and such other molecules are likely to provide insights into the molecular mechanisms that control stem cell fate, and may ultimately be useful to in vivo stem cell biology and therapy.
为了更好地理解和控制调节干细胞命运的过程,我们着手鉴定能够诱导胚胎干细胞(ESC)向神经元分化的小分子。基于激酶导向组合文库的高通量细胞表型筛选发现了TWS119,一种4,6-二取代的吡咯并嘧啶,它能够诱导小鼠胚胎干细胞发生神经生成。通过基于亲和力的方法和生化方法均表明,TWS119的作用靶点是糖原合酶激酶-3β(GSK-3β)。这项研究提供了证据,证明GSK-3β参与了胚胎干细胞中哺乳动物神经生成的诱导过程。此类分子可能会为控制干细胞命运的分子机制提供深入了解,并且最终可能对体内干细胞生物学和治疗有用。