Acheson Jordan, Joanisse Sophie, Sale Craig, Hodson Nathan
Department of Sport and Exercise Sciences, Manchester Metropolitan University, Institute of Sport, Manchester, U.K.
School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, U.K.
Biosci Rep. 2025 Jan 30;45(1):1-30. doi: 10.1042/BSR20240137.
Skeletal muscle is a highly plastic tissue that can adapt relatively rapidly to a range of stimuli. In response to novel mechanical loading, e.g. unaccustomed resistance exercise, myofibers are disrupted and undergo a period of ultrastructural remodeling to regain full physiological function, normally within 7 days. The mechanisms that underpin this remodeling are believed to be a combination of cellular processes including ubiquitin-proteasome/calpain-mediated degradation, immune cell infiltration, and satellite cell proliferation/differentiation. A relatively understudied system that has the potential to be a significant contributing mechanism to repair and recovery is the autophagolysosomal system, an intracellular process that degrades damaged and redundant cellular components to provide constituent metabolites for the resynthesis of new organelles and cellular structures. This review summarizes our current understanding of the autophagolysosomal system in the context of skeletal muscle repair and recovery. In addition, we also provide hypothetical models of how this system may interact with other processes involved in skeletal muscle remodeling and provide avenues for future research to improve our understanding of autophagy in human skeletal muscle.
骨骼肌是一种高度可塑性的组织,能够相对迅速地适应一系列刺激。响应新的机械负荷,例如不习惯的抗阻运动,肌纤维会受到破坏,并经历一段超微结构重塑期,通常在7天内恢复完全的生理功能。据信,支撑这种重塑的机制是多种细胞过程的组合,包括泛素-蛋白酶体/钙蛋白酶介导的降解、免疫细胞浸润以及卫星细胞增殖/分化。自噬溶酶体系统是一个相对未被充分研究的系统,它有可能是修复和恢复的一个重要促成机制,这是一个细胞内过程,可降解受损和多余的细胞成分,为新细胞器和细胞结构的重新合成提供组成代谢物。本综述总结了我们目前在骨骼肌修复和恢复背景下对自噬溶酶体系统的理解。此外,我们还提供了该系统可能如何与参与骨骼肌重塑的其他过程相互作用的假设模型,并为未来研究提供途径,以增进我们对人类骨骼肌自噬的理解。