Masschelein Evi, D'Hulst Gommaar, Zvick Joel, Hinte Laura, Soro-Arnaiz Inés, Gorski Tatiane, von Meyenn Ferdinand, Bar-Nur Ori, De Bock Katrien
Department Health Sciences and Technology, Laboratory of Exercise and Health, Swiss Federal Institute of Technology (ETH) Zurich, Zurich, Switzerland.
Department Health Sciences and Technology, Laboratory of Regenerative and Movement Biology, Swiss Federal Institute of Technology (ETH) Zurich, Zurich, Switzerland.
Skelet Muscle. 2020 Jul 9;10(1):21. doi: 10.1186/s13395-020-00237-2.
Satellite cells (SCs) are required for muscle repair following injury and are involved in muscle remodeling upon muscular contractions. Exercise stimulates SC accumulation and myonuclear accretion. To what extent exercise training at different mechanical loads drive SC contribution to myonuclei however is unknown.
By performing SC fate tracing experiments, we show that 8 weeks of voluntary wheel running increased SC contribution to myofibers in mouse plantar flexor muscles in a load-dependent, but fiber type-independent manner. Increased SC fusion however was not exclusively linked to muscle hypertrophy as wheel running without external load substantially increased SC fusion in the absence of fiber hypertrophy. Due to nuclear propagation, nuclear fluorescent fate tracing mouse models were inadequate to quantify SC contribution to myonuclei. Ultimately, by performing fate tracing at the DNA level, we show that SC contribution mirrors myonuclear accretion during exercise.
Collectively, mechanical load during exercise independently promotes SC contribution to existing myofibers. Also, due to propagation of nuclear fluorescent reporter proteins, our data warrant caution for the use of existing reporter mouse models for the quantitative evaluation of satellite cell contribution to myonuclei.
卫星细胞(SCs)是损伤后肌肉修复所必需的,并且参与肌肉收缩时的肌肉重塑。运动刺激卫星细胞积累和肌核增加。然而,不同机械负荷下的运动训练在多大程度上驱动卫星细胞对肌核的贡献尚不清楚。
通过进行卫星细胞命运追踪实验,我们发现8周的自主轮转跑步以负荷依赖但纤维类型独立的方式增加了小鼠跖屈肌中卫星细胞对肌纤维的贡献。然而,卫星细胞融合增加并不完全与肌肉肥大相关,因为无外部负荷的轮转跑步在无纤维肥大的情况下显著增加了卫星细胞融合。由于核传播,核荧光命运追踪小鼠模型不足以量化卫星细胞对肌核的贡献。最终,通过在DNA水平进行命运追踪,我们发现卫星细胞的贡献反映了运动期间的肌核增加。
总体而言,运动期间的机械负荷独立促进卫星细胞对现有肌纤维的贡献。此外,由于核荧光报告蛋白的传播,我们的数据提醒在使用现有报告小鼠模型定量评估卫星细胞对肌核的贡献时要谨慎。