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Exercise rejuvenates quiescent skeletal muscle stem cells in old mice through restoration of Cyclin D1

机译:交感神经运动静止的骨骼肌干细胞通过恢复老老鼠细胞周期蛋白D1

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摘要

Ageing impairs tissue repair. This defect is pronounced in skeletal muscle, whose regeneration by muscle stem cells (MuSCs) is robust in young-adult animals, but inefficient in older organisms. Despite this functional decline, old MuSCs are amenable to rejuvenation through strategies that improve the systemic milieu, such as heterochronic parabiosis. One such strategy, exercise, has long been appreciated for its benefits on healthspan, but its effects on aged stem-cell function in the context of tissue regeneration are incompletely understood. Here, we show that exercise in the form of voluntary wheel running accelerates muscle repair in old mice and improves old MuSC function. Through transcriptional profiling and genetic studies, we discovered that the restoration of old MuSC activation ability hinges on restoration of Cyclin D1, whose expression declines with age in MuSCs. Pharmacologic studies revealed that Cyclin D1 maintains MuSC activation capacity by repressing TGF-beta signalling. Taken together, these studies demonstrate that voluntary exercise is a practicable intervention for old MuSC rejuvenation. Furthermore, this work highlights the distinct role of Cyclin D1 in stem-cell quiescence.
机译:老龄化会损害组织修复。在骨骼肌的再生由肌肉干细胞(音乐)是健壮的年轻人常见的动物,但在老效率低下生物。音乐是能够复兴等策略,提高了系统的环境作为heterochronic异种共生。锻炼,一直感激它在健寿好处,但对年龄的影响干细胞功能的组织再生不完全理解。我们表明,运动的形式自愿的轮运行加速肌肉修复旧老鼠和改善旧音乐功能。转录分析和遗传研究,我们发现恢复旧的音乐激活的能力取决于恢复细胞周期蛋白D1的表达会随着年龄的增长而减少音乐。D1维护音乐激活能力抑制及信号。这些研究表明,自愿的运动是一个可行的干预旧音乐吗复兴。干细胞的细胞周期蛋白D1的截然不同的角色静止。

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