Muscle Health Research Centre, School of Kinesiology and Health Science, York University, Toronto, Ontario, M3J 1P3, Canada.
Department of Biology, York University, Toronto, Ontario, M3J 1P3, Canada.
J Physiol. 2018 Aug;596(16):3567-3584. doi: 10.1113/JP275998. Epub 2018 Jul 3.
A healthy mitochondrial pool is dependent on the removal of dysfunctional organelles via mitophagy, but little is known about how mitophagy is altered with ageing and chronic exercise. Chronic contractile activity (CCA) is a standardized exercise model that can elicit mitochondrial adaptations in both young and aged muscle, albeit to a lesser degree in the aged group. Assessment of mitophagy flux revealed enhanced targeting of mitochondria for degradation in aged muscle, in contrast to previous theories. Mitophagy flux was significantly reduced as an adaptation to CCA suggesting that an improvement in organelle quality reduces the need for mitochondrial turnover. CCA enhances lysosomal capacity and may ameliorate lysosomal dysfunction in aged muscle.
Skeletal muscle exhibits deficits in mitochondrial quality with age. Central to the maintenance of a healthy mitochondrial pool is the removal of dysfunctional organelles via mitophagy. Little is known on how mitophagy is altered with ageing and chronic exercise. We assessed mitophagy flux using colchicine treatment in vivo following chronic contractile activity (CCA) of muscle in young and aged rats. CCA evoked mitochondrial biogenesis in young muscle, with an attenuated response in aged muscle. Mitophagy flux was higher in aged muscle and was correlated with the enhanced expression of mitophagy receptors and upstream transcriptional regulators. CCA decreased mitophagy flux in both age groups, suggesting an improvement in organelle quality. CCA also reduced the exaggerated expression of TFEB evident in aged muscle, which may be promoting the age-induced increase in lysosomal markers. Thus, aged muscle possesses an elevated drive for autophagy and mitophagy which may contribute to the decline in organelle content observed with age, but which may serve to maintain mitochondrial quality. CCA improves organelle integrity and reduces mitophagy, illustrating that chronic exercise is a modality to improve muscle quality in aged populations.
健康的线粒体池依赖于通过自噬作用清除功能失调的细胞器,但对于衰老和慢性运动如何改变自噬作用知之甚少。慢性收缩性活动(CCA)是一种标准化的运动模型,可引起年轻和老年肌肉中的线粒体适应,尽管在老年组中的适应程度较小。自噬通量的评估显示,衰老肌肉中靶向降解的线粒体增加,与以前的理论相反。自噬通量作为 CCA 的适应显著降低,表明细胞器质量的提高减少了对线粒体周转的需求。CCA 增强溶酶体的能力,并可能改善衰老肌肉中的溶酶体功能障碍。
骨骼肌随年龄增长表现出线粒体质量缺陷。维持健康的线粒体池的核心是通过自噬作用清除功能失调的细胞器。对于衰老和慢性运动如何改变自噬作用知之甚少。我们使用秋水仙碱在体内处理,评估了年轻和老年大鼠肌肉慢性收缩性活动(CCA)后的自噬通量。CCA 在年轻肌肉中引发了线粒体生物发生,而在老年肌肉中的反应减弱。衰老肌肉中的自噬通量更高,并且与自噬受体和上游转录调节因子的增强表达相关。CCA 降低了两个年龄组的自噬通量,表明细胞器质量的提高。CCA 还降低了在衰老肌肉中明显增加的 TFEB 的表达,这可能促进了溶酶体标记物的年龄诱导增加。因此,衰老肌肉具有更高的自噬和线粒体自噬驱动力,这可能导致随着年龄增长观察到的细胞器含量下降,但可能有助于维持线粒体质量。CCA 可改善细胞器完整性并减少自噬作用,表明慢性运动是改善老年人群肌肉质量的一种方式。