Institute for Stem Cell Research, MRC Centre for Regenerative Medicine, The University of Edinburgh, Edinburgh EH16 4UU, UK.
Cell Rep. 2013 Feb 21;3(2):472-84. doi: 10.1016/j.celrep.2013.01.017. Epub 2013 Feb 7.
The events that prime pluripotent cells for differentiation are not well understood. Inhibitor of DNA binding/differentiation (Id) proteins, which are inhibitors of basic helix-loop-helix (bHLH) transcription factor activity, contribute to pluripotency by blocking sequential transitions toward differentiation. Using yeast-two-hybrid screens, we have identified Id-regulated transcription factors that are expressed in embryonic stem cells (ESCs). One of these, Tcf15, is also expressed in the embryonic day 4.5 embryo and is specifically associated with a novel subpopulation of primed ESCs. An Id-resistant form of Tcf15 rapidly downregulates Nanog and accelerates somatic lineage commitment. We propose that because Tcf15 can be held in an inactive state through Id activity, it may prime pluripotent cells for entry to somatic lineages upon downregulation of Id. We also find that Tcf15 expression is dependent on fibroblast growth factor (FGF) signaling, providing an explanation for how FGF can prime for differentiation without driving cells out of the pluripotent state.
多能干细胞向分化方向启动的机制目前还不完全清楚。DNA 结合/分化抑制因子(Id)蛋白是碱性螺旋-环-螺旋(bHLH)转录因子活性的抑制剂,通过阻止多能干细胞向分化方向的连续转变,从而维持其多能性。利用酵母双杂交筛选,我们已经鉴定出在胚胎干细胞(ESC)中表达的由 Id 调控的转录因子。其中一个转录因子 Tcf15 也在胚胎发育第 4.5 天的胚胎中表达,并且与一个新的、处于初始状态的 ESC 亚群特异性相关。Id 抗性形式的 Tcf15 可以快速下调 Nanog 并加速体细胞谱系的确定。我们提出,由于 Tcf15 的活性可以通过 Id 蛋白的活性被抑制,因此当 Id 蛋白下调时,Tcf15 可能会使多能细胞为进入体细胞谱系做好准备。我们还发现,Tcf15 的表达依赖于成纤维细胞生长因子(FGF)信号,这也解释了为什么 FGF 可以在不使细胞脱离多能状态的情况下为分化做好准备。