Epigenetics Programme, The Babraham Institute, Cambridge, UK; Mass Spectrometry Facility, The Babraham Institute, Cambridge, UK.
Epigenetics Programme, The Babraham Institute, Cambridge, UK.
Stem Cell Reports. 2020 May 12;14(5):972-988. doi: 10.1016/j.stemcr.2020.03.017. Epub 2020 Apr 16.
Naive and primed human pluripotent stem cells (hPSC) provide valuable models to study cellular and molecular developmental processes. The lack of detailed information about cell-surface protein expression in these two pluripotent cell types prevents an understanding of how the cells communicate and interact with their microenvironments. Here, we used plasma membrane profiling to directly measure cell-surface protein expression in naive and primed hPSC. This unbiased approach quantified over 1,700 plasma membrane proteins, including those involved in cell adhesion, signaling, and cell interactions. Notably, multiple cytokine receptors upstream of JAK-STAT signaling were more abundant in naive hPSC. In addition, functional experiments showed that FOLR1 and SUSD2 proteins are highly expressed at the cell surface in naive hPSC but are not required to establish human naive pluripotency. This study provides a comprehensive stem cell proteomic resource that uncovers differences in signaling pathway activity and has identified new markers to define human pluripotent states.
幼稚态和起始态的人类多能干细胞(hPSC)为研究细胞和分子发育过程提供了有价值的模型。由于缺乏这两种多能细胞类型中关于细胞表面蛋白表达的详细信息,因此无法了解细胞如何与其微环境进行通信和相互作用。在这里,我们使用质膜蛋白组学直接测量幼稚态和起始态 hPSC 的细胞表面蛋白表达。这种无偏倚的方法定量了超过 1700 种质膜蛋白,包括参与细胞黏附、信号转导和细胞相互作用的蛋白。值得注意的是,JAK-STAT 信号通路上游的多种细胞因子受体在幼稚态 hPSC 中更为丰富。此外,功能实验表明,FOLR1 和 SUSD2 蛋白在幼稚态 hPSC 的细胞表面高度表达,但对于建立人类幼稚多能性并非必需。本研究提供了一个全面的干细胞蛋白质组资源,揭示了信号通路活性的差异,并确定了新的标记物来定义人类多能状态。