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Cell-Surface Proteomics Identifies Differences in Signaling and Adhesion Protein Expression between Naive and Primed Human Pluripotent Stem Cells

机译:细胞表面蛋白质组学鉴定了幼稚和灌注人多能干细胞之间的信号传导和粘附蛋白表达的差异

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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.
机译:Naive和Primed人多能干细胞(HPSC)提供了有价值的模型,以研究细胞和分子发育过程。在这两种多能细胞类型中缺乏有关细胞表面蛋白表达的详细信息可防止对细胞的通信和与其微环境相互作用的理解。在此,我们使用血浆膜分析直接测量幼稚和灌注HPSC中的细胞表面蛋白表达。这种无偏异的方法量化超过1,700种血浆膜蛋白,包括参与细胞粘附,信号传导和细胞相互作用的蛋白质。值得注意的是,在jak-stat信号传导上游的多种细胞因子受体在幼稚HPSC中更丰富。此外,功能实验表明,Folr1和SuSD2蛋白在幼稚HPSC中的细胞表面上高度表达,但不需要建立人幼稚多能性。本研究提供了一种综合的干细胞蛋白质组学资源,揭示了信号通路活动的差异,并确定了新标志物以定义人类多能态。

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