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  • 标题:Troy+ brain stem cells cycle through quiescence and regulate their number by sensing niche occupancy
  • 本地全文:下载
  • 作者:Onur Basak ; Teresa G. Krieger ; Mauro J. Muraro
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2018
  • 卷号:115
  • 期号:4
  • 页码:E610-E619
  • DOI:10.1073/pnas.1715911114
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:The adult mouse subependymal zone provides a niche for mammalian neural stem cells (NSCs). However, the molecular signature, self-renewal potential, and fate behavior of NSCs remain poorly defined. Here we propose a model in which the fate of active NSCs is coupled to the total number of neighboring NSCs in a shared niche. Using knock-in reporter alleles and single-cell RNA sequencing, we show that the Wnt target Tnfrsf19/ Troy identifies both active and quiescent NSCs. Quantitative analysis of genetic lineage tracing of individual NSCs under homeostasis or in response to injury reveals rapid expansion of stem-cell number before some return to quiescence. This behavior is best explained by stochastic fate decisions, where stem-cell number within a shared niche fluctuates over time. Fate mapping proliferating cells using a Ki67iresCreER allele confirms that active NSCs reversibly return to quiescence, achieving long-term self-renewal. Our findings suggest a niche-based mechanism for the regulation of NSC fate and number.
  • 关键词:neural stem cells ; cellular dynamics ; modeling ; single-cell sequencing ; ki67
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