Collier Amanda J, Panula Sarita P, Schell John Paul, Chovanec Peter, Plaza Reyes Alvaro, Petropoulos Sophie, Corcoran Anne E, Walker Rachael, Douagi Iyadh, Lanner Fredrik, Rugg-Gunn Peter J
Epigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK; Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 1QR, UK.
Department of Clinical Science, Intervention, and Technology, Karolinska Institutet, 14186 Stockholm, Sweden; Division of Obstetrics and Gynecology, Karolinska Universitetssjukhuset, 14186 Stockholm, Sweden.
Cell Stem Cell. 2017 Jun 1;20(6):874-890.e7. doi: 10.1016/j.stem.2017.02.014. Epub 2017 Mar 23.
Human pluripotent stem cells (PSCs) exist in naive and primed states and provide important models to investigate the earliest stages of human development. Naive cells can be obtained through primed-to-naive resetting, but there are no reliable methods to prospectively isolate unmodified naive cells during this process. Here we report comprehensive profiling of cell surface proteins by flow cytometry in naive and primed human PSCs. Several naive-specific, but not primed-specific, proteins were also expressed by pluripotent cells in the human preimplantation embryo. The upregulation of naive-specific cell surface proteins during primed-to-naive resetting enabled the isolation and characterization of live naive cells and intermediate cell populations. This analysis revealed distinct transcriptional and X chromosome inactivation changes associated with the early and late stages of naive cell formation. Thus, identification of state-specific proteins provides a robust set of molecular markers to define the human PSC state and allows new insights into the molecular events leading to naive cell resetting.
人类多能干细胞(PSC)以原始态和始发态存在,为研究人类发育的最早阶段提供了重要模型。原始态细胞可通过从始发态到原始态的重编程获得,但在此过程中尚无可靠方法可前瞻性地分离未修饰的原始态细胞。在此,我们报告了通过流式细胞术对原始态和始发态人类PSC的细胞表面蛋白进行的全面分析。人类植入前胚胎中的多能细胞也表达了几种原始态特异性而非始发态特异性的蛋白。在从始发态到原始态的重编程过程中,原始态特异性细胞表面蛋白的上调使得能够分离和鉴定活的原始态细胞及中间细胞群体。该分析揭示了与原始态细胞形成的早期和晚期相关的不同转录和X染色体失活变化。因此,鉴定状态特异性蛋白提供了一组强大的分子标记来定义人类PSC状态,并有助于深入了解导致原始态细胞重编程的分子事件。