Romanello Vanina, Sandri Marco
Veneto Institute of Molecular Medicine, via Orus 2, 35129 Padova, Italy; Department of Biomedical Sciences, University of Padova, via G. Colombo 3, 35100 Padova, Italy.
Veneto Institute of Molecular Medicine, via Orus 2, 35129 Padova, Italy; Department of Biomedical Sciences, University of Padova, via G. Colombo 3, 35100 Padova, Italy; Department of Medicine, McGill University, Montreal, Canada.
Semin Cell Dev Biol. 2023 Jul 15;143:46-53. doi: 10.1016/j.semcdb.2022.02.011. Epub 2022 Feb 12.
The continuous dynamic reshaping of mitochondria by fusion and fission events is critical to keep mitochondrial quality and function under control in response to changes in energy and stress. Maintaining a functional, highly interconnected mitochondrial reticulum ensures rapid energy production and distribution. Moreover, mitochondrial networks act as dynamic signaling hub to adapt to the metabolic demands imposed by contraction, energy expenditure, and general metabolism. However, excessive mitochondrial fusion or fission results in the disruption of the skeletal muscle mitochondrial network integrity and activates a retrograde response from mitochondria to the nucleus, leading to muscle atrophy, weakness and influencing whole-body homeostasis. These actions are mediated via the secretion of mitochondrial-stress myokines such as FGF21 and GDF15. Here we will summarize recent discoveries in the role of mitochondrial fusion and fission in the control of muscle mass and in regulating physiological homeostasis and disease progression.
线粒体通过融合和分裂事件进行的持续动态重塑对于在能量和应激变化时控制线粒体质量和功能至关重要。维持一个功能性的、高度相互连接的线粒体网状结构可确保能量的快速产生和分配。此外,线粒体网络作为动态信号枢纽,以适应收缩、能量消耗和一般代谢所带来的代谢需求。然而,过度的线粒体融合或分裂会导致骨骼肌线粒体网络完整性的破坏,并激活线粒体向细胞核的逆行反应,导致肌肉萎缩、无力,并影响全身稳态。这些作用是通过分泌线粒体应激肌动蛋白如FGF21和GDF15介导的。在这里,我们将总结线粒体融合和分裂在控制肌肉质量以及调节生理稳态和疾病进展方面作用的最新发现。