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Human skeletal muscle ageing atlas

老化 骨骼肌 肌萎缩 心肌细胞 生物 细胞生物学 人口 解剖 医学 遗传学 环境卫生
作者
Veronika R. Kedlian,Yaning Wang,Tianliang Liu,Xiaoping Chen,Liam Bolt,Zhuo Shen,Eirini S. Fasouli,Elena Prigmore,Vitalii Kleshchevnikov,Tong Li,John S. Lawrence,Ni Huang,Qin Guo,Lu Yang,Krzysztof Polański,Monika Dąbrowska,Catherine Tudor,Xiaobo Li,Ömer Bayraktar,Minal Patel,Kerstin B. Meyer,Natsuhiko Kumasaka,Krishnaa Mahbubani,Andy Peng Xiang,Kourosh Saeb‐Parsy,Sarah A. Teichmann,Hongbo Zhang
标识
DOI:10.1101/2022.05.24.493094
摘要

Abstract Skeletal muscle ageing increases the incidence of age-associated frailty and sarcopenia in the elderly worldwide, leading to increased morbidity and mortality. However, our understanding of the cellular and molecular mechanisms of muscle ageing is still far from complete. Here, we generate a single-cell and single-nucleus transcriptomic atlas of skeletal muscle ageing from 15 donors across the adult human lifespan, accompanied by myofiber typing using imaging. Our atlas reveals ageing mechanisms acting across different compartments of the muscle, including muscle stem cells (MuSCs), myofibers and the muscle microenvironment. Firstly, we uncover two mechanisms driving MuSC ageing, namely a decrease in ribosome biogenesis and an increase in inflammation. Secondly, we identify a set of nuclei populations explaining the preferential degeneration of the fast-twitch myofibers and suggest two mechanisms acting to compensate for their loss. Importantly, we identify a neuromuscular junction accessory population, which helps myofiber to compensate for aged-related denervation. Thirdly, we reveal multiple microenvironment cell types contributing to the inflammatory milieu of ageing muscle by producing cytokines and chemokines to attract immune cells. Finally, we provide a comparable mouse muscle ageing atlas and further investigate conserved and specific ageing hallmarks across species. In summary, we present a comprehensive human skeletal muscle ageing resource by combining different data modalities, which significantly expands our understanding of muscle biology and ageing.
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