干细胞
转录组
生物
细胞生物学
电池类型
细胞
干细胞衰老理论
造血
成体干细胞
再生(生物学)
细胞分化
神经科学
干细胞因子
基因表达
遗传学
基因
作者
Ling Liu,Soochi Kim,Matthew T. Buckley,Jaime M. Reyes,Jengmin Kang,Lei Tian,Mingqiang Wang,Alexander Lieu,Michelle Mao,Cristina Rodríguez-Mateo,Heather D. Ishak,Mira Jeong,Joseph C. Wu,Margaret A. Goodell,Anne Brunet,Thomas A. Rando
标识
DOI:10.1101/2022.01.12.475145
摘要
ABSTRACT Exercise has the ability to rejuvenate stem cells and improve tissue homeostasis and regeneration in aging animals. However, the cellular and molecular changes elicited by exercise have not been systematically studied across a broad range of cell types in stem cell compartments. To gain better insight into the mechanisms by which exercise affects niche and stem cell function, we subjected young and old mice to aerobic exercise and generated a single cell transcriptomic atlas of muscle, neural and hematopoietic stem cells with their niche cells and progeny. Complementarily, we also performed whole transcriptome analysis of single myofibers from these animals. We identified common and unique pathways that are compromised across these tissues and cell types in aged animals. We found that exercise has a rejuvenating effect on subsets of stem cells, and a profound impact in the composition and transcriptomic landscape of both circulating and tissue resident immune cells. Exercise ameliorated the upregulation of a number of inflammatory pathways as well as restored aspects of cell-cell communication within these stem cell compartments. Our study provides a comprehensive view of the coordinated responses of multiple aged stem cells and niche cells to exercise at the transcriptomic level.
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