Muscle Health Research Centre, York University, Toronto, ON M3J 1P3, Canada.
School of Kinesiology and Health Science, York University, Toronto, ON M3J 1P3, Canada.
Cells. 2021 Apr 29;10(5):1054. doi: 10.3390/cells10051054.
Sarcopenia is the loss of both muscle mass and function with age. Although the molecular underpinnings of sarcopenia are not fully understood, numerous pathways are implicated, including autophagy, in which defective cargo is selectively identified and degraded at the lysosome. The specific tagging and degradation of mitochondria is termed mitophagy, a process important for the maintenance of an organelle pool that functions efficiently in energy production and with relatively low reactive oxygen species production. Emerging data, yet insufficient, have implicated various steps in this pathway as potential contributors to the aging muscle atrophy phenotype. Included in this is the lysosome, the end-stage organelle possessing a host of proteolytic and degradative enzymes, and a function devoted to the hydrolysis and breakdown of defective molecular complexes and organelles. This review provides a summary of our current understanding of how the autophagy-lysosome system is regulated in aging muscle, highlighting specific areas where knowledge gaps exist. Characterization of the autophagy pathway with a particular focus on the lysosome will undoubtedly pave the way for the development of novel therapeutic strategies to combat age-related muscle loss.
肌肉减少症是随着年龄增长而发生的肌肉质量和功能的丧失。虽然肌肉减少症的分子基础尚未完全清楚,但许多途径都与之相关,包括自噬,在自噬中,有缺陷的货物在溶酶体中被选择性地识别和降解。线粒体的特定标记和降解称为线粒体自噬,这是维持细胞器池的重要过程,该细胞器池在能量产生方面有效且相对低产生活性氧物种。新出现的、但还不够充分的数据表明,该途径的各个步骤都可能是导致衰老肌肉萎缩表型的潜在因素。其中包括溶酶体,这是一种具有多种蛋白水解和降解酶的终末细胞器,其功能专门用于水解和分解有缺陷的分子复合物和细胞器。本文综述了我们目前对衰老肌肉中自噬溶酶体系统如何调节的理解,强调了存在知识空白的特定领域。对自噬途径的特征分析,特别是对溶酶体的分析,无疑将为开发针对与年龄相关的肌肉丧失的新型治疗策略铺平道路。