Li Yu-Qiang
Cell Laboratory, Marine College, Shandong University at Weihai, Shandong, People's Republic of China.
Cell Reprogram. 2010 Feb;12(1):3-13. doi: 10.1089/cell.2009.0033.
The present article reviews master stem cell transcription factors, their expression regulation network, and related signaling pathways with the aim of understanding the molecular mechanisms of pluripotent cell fate decisions. Oct4, Sox2, and Nanog are master transcription factors for maintenance of the undifferentiated state and self-renewal of embryonic stem cells (ESCs). In the mouse, they form a regulatory circuitry with coregulators, such as beta-catenin, Stat3, Myc, Klfs, Sall4, and Esrrb to control the expression of pluripotency-related genes including themselves. The threshold expression of Oct4, Sox2, and Nanog for sustaining ESC properties depends on the synergistic effects among Stat3, beta-catenin, and Smad signaling pathway under the specific conditions of the ESC cytoplasmic microenvironment. Some of the salient differences in human ESC signaling pathways affecting their fate commitment are highlighted.
本文综述了主干细胞转录因子、它们的表达调控网络以及相关信号通路,旨在了解多能细胞命运决定的分子机制。Oct4、Sox2和Nanog是维持胚胎干细胞(ESC)未分化状态和自我更新的主转录因子。在小鼠中,它们与β-连环蛋白、Stat3、Myc、Klfs、Sall4和Esrrb等共调节因子形成一个调控回路,以控制包括它们自身在内的多能性相关基因的表达。在ESC细胞质微环境的特定条件下,维持ESC特性所需的Oct4、Sox2和Nanog的阈值表达取决于Stat3、β-连环蛋白和Smad信号通路之间的协同作用。文中强调了影响人类ESC命运决定的信号通路中的一些显著差异。