Translational Medical Center for Stem Cell Therapy & Institute for Regenerative Medicine, Shanghai East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai 200120, China; Frontier Science Center for Stem Cell Research, Tongji University, Shanghai 200092, China.
Translational Medical Center for Stem Cell Therapy & Institute for Regenerative Medicine, Shanghai East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai 200120, China; Frontier Science Center for Stem Cell Research, Tongji University, Shanghai 200092, China.
Cell Rep. 2023 Apr 25;42(4):112379. doi: 10.1016/j.celrep.2023.112379. Epub 2023 Apr 11.
Over the past few decades, many attempts have been made to capture different states of pluripotency in vitro. Naive and primed pluripotent stem cells, corresponding to the pluripotency states of pre- and post-implantation epiblasts, respectively, have been well characterized in mice and can be interconverted in vitro. Here, we summarize the recently reported strategies to generate human naive pluripotent stem cells in vitro. We discuss their applications in studies of regulatory mechanisms involved in early developmental processes, including identification of molecular features, X chromosome inactivation modeling, transposable elements regulation, metabolic characteristics, and cell fate regulation, as well as potential for extraembryonic differentiation and blastoid construction for embryogenesis modeling. We further discuss the naive pluripotency-related research, including 8C-like cell establishment and disease modeling. We also highlight limitations of current naive pluripotency studies, such as imperfect culture conditions and inadequate responsiveness to differentiation signals.
在过去的几十年中,人们已经尝试了许多方法来在体外捕获不同的多能性状态。原始态和初始态多能干细胞分别对应于着床前外胚层的多能性状态,在小鼠中得到了很好的描述,并可以在体外相互转化。在这里,我们总结了最近报道的在体外生成人类原始态多能干细胞的策略。我们讨论了它们在研究早期发育过程中涉及的调控机制中的应用,包括鉴定分子特征、X 染色体失活建模、转座元件调控、代谢特征和细胞命运调控,以及用于胚胎发生建模的胚外分化和类胚体构建的潜力。我们进一步讨论了与原始态多能性相关的研究,包括 8C 样细胞的建立和疾病建模。我们还强调了当前原始态多能性研究的局限性,例如培养条件不完善和对分化信号的反应不足。