Stem Cell and Cancer Research Institute, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
Stem Cells. 2010 Mar 31;28(3):419-30. doi: 10.1002/stem.298.
Pluripotent stem cells (PSCs) have been derived from the embryos of mice and humans, representing the two major sources of PSCs. These cells are universally defined by their developmental properties, specifically their self-renewal capacity and differentiation potential which are regulated in mice and humans by complex transcriptional networks orchestrated by conserved transcription factors. However, significant differences exist in the transcriptional networks and signaling pathways that control mouse and human PSC self-renewal and lineage development. To distinguish between universally applicable and species-specific features, we collated and compared the molecular and cellular descriptions of mouse and human PSCs. Here we compare and contrast the response to signals dictated by the transcriptome and epigenome of mouse and human PSCs that will hopefully act as a critical resource to the field. These analyses underscore the importance of accounting for species differences when designing strategies to capitalize on the clinical potential of human PSCs.
多能干细胞(PSCs)已从老鼠和人类的胚胎中被分离出来,代表了 PSCs 的两个主要来源。这些细胞的发育特性使其具有普遍性,特别是自我更新能力和分化潜能,在老鼠和人类中,由受保守转录因子调控的复杂转录网络调控。然而,控制老鼠和人类 PSC 自我更新和谱系发育的转录网络和信号通路存在显著差异。为了区分普遍适用和物种特异性的特征,我们收集并比较了老鼠和人类 PSC 的分子和细胞描述。在这里,我们比较和对比了由老鼠和人类 PSCs 的转录组和表观基因组决定的信号的反应,希望这将成为该领域的一个重要资源。这些分析强调了在设计利用人类 PSC 的临床潜力的策略时,考虑物种差异的重要性。