Betschinger Joerg
Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland.
J Mol Biol. 2017 May 19;429(10):1441-1458. doi: 10.1016/j.jmb.2016.12.017. Epub 2016 Dec 21.
The formation of tissues and organs during metazoan development begs fundamental questions of cellular plasticity: How can the very same genome program have diverse cell types? How do cell identity programs unfold during development in space and time? How can defects in these mechanisms cause disease and also provide opportunities for therapeutic intervention? And ultimately, can developmental programs be exploited for bioengineering tissues and organs? Understanding principle designs of cellular identity and developmental progression is crucial for providing answers. Here, I will discuss how the capture of embryonic pluripotency in murine embryonic stem cells (ESCs) in vitro has allowed fundamental insights into the molecular underpinnings of a developmental cell state and how its ordered disassembly during differentiation prepares for lineage specification.
相同的基因组程序如何产生多种细胞类型?细胞身份程序在发育过程中如何在空间和时间上展开?这些机制中的缺陷如何导致疾病,又如何为治疗干预提供机会?最终,发育程序能否用于生物工程组织和器官?理解细胞身份和发育进程的基本设计对于提供答案至关重要。在这里,我将讨论在体外捕获小鼠胚胎干细胞(ESC)中的胚胎多能性如何使我们对发育细胞状态的分子基础有了基本认识,以及其在分化过程中有序解体如何为谱系特化做准备。