Laboratory of Neural Plasticity, Faculties of Medicine and Science, Brain Research Institute, University of Zurich, 8057 Zurich, Switzerland.
Institute for Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany.
Cell Stem Cell. 2021 Nov 4;28(11):2020-2034.e12. doi: 10.1016/j.stem.2021.08.012. Epub 2021 Sep 14.
The division potential of individual stem cells and the molecular consequences of successive rounds of proliferation remain largely unknown. Here, we developed an inducible cell division counter (iCOUNT) that reports cell division events in human and mouse tissues in vitro and in vivo. Analyzing cell division histories of neural stem/progenitor cells (NSPCs) in the developing and adult brain, we show that iCOUNT can provide novel insights into stem cell behavior. Further, we use single-cell RNA sequencing (scRNA-seq) of iCOUNT-labeled NSPCs and their progenies from the developing mouse cortex and forebrain-regionalized human organoids to identify functionally relevant molecular pathways that are commonly regulated between mouse and human cells, depending on individual cell division histories. Thus, we developed a tool to characterize the molecular consequences of repeated cell divisions of stem cells that allows an analysis of the cellular principles underlying tissue formation, homeostasis, and repair.
单个干细胞的分裂潜能和连续增殖的分子后果在很大程度上仍然未知。在这里,我们开发了一种可诱导的细胞分裂计数器(iCOUNT),可以在体外和体内报告人和小鼠组织中的细胞分裂事件。在分析发育中和成年大脑中的神经干细胞/祖细胞(NSPC)的细胞分裂历史时,我们表明 iCOUNT 可以为干细胞行为提供新的见解。此外,我们使用单细胞 RNA 测序(scRNA-seq)对来自发育中的小鼠皮层和大脑区域特化的人类类器官的 iCOUNT 标记的 NSPC 及其后代进行分析,以确定功能相关的分子途径,这些途径在取决于个体细胞分裂历史的情况下,在小鼠和人类细胞之间受到共同调节。因此,我们开发了一种工具来描述干细胞多次分裂的分子后果,这允许分析组织形成、稳态和修复的细胞原理。