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线粒体生物发生和碎片化作为肌肉蛋白降解的调节剂。

Mitochondrial biogenesis and fragmentation as regulators of muscle protein degradation.

机构信息

Dulbecco Telethon Institute at Venetian Institute of Molecular Medicine, via Orus 2, 35129 Padova, Italy.

出版信息

Curr Hypertens Rep. 2010 Dec;12(6):433-9. doi: 10.1007/s11906-010-0157-8.

DOI:10.1007/s11906-010-0157-8
PMID:20967516
Abstract

Mitochondria form a dynamic network that rapidly adapts to cellular energy demand. This adaptation is particularly important in skeletal muscle because of its high metabolic rate. Indeed, muscle energy level is one of the cellular checkpoints that lead either to sustained protein synthesis and growth or protein breakdown and atrophy. Mitochondrial function is affected by changes in shape, number, and localization. The dynamics that control the mitochondrial network, such as biogenesis and fusion, or fragmentation and fission, ultimately affect the signaling pathways that regulate muscle mass. Regular exercise and healthy muscles are important players in the metabolic control of human body. Indeed, a sedentary lifestyle is detrimental for muscle function and is one of the major causes of metabolic disorders such as obesity and diabetes. This article reviews the rapid progress made in the past few years regarding the role of mitochondria in the control of proteolytic systems and in the loss of muscle mass and function.

摘要

线粒体形成一个动态网络,能够迅速适应细胞的能量需求。这种适应性在骨骼肌中尤为重要,因为骨骼肌的代谢率很高。事实上,肌肉的能量水平是细胞的检测点之一,它可以导致持续的蛋白质合成和生长,也可以导致蛋白质分解和萎缩。线粒体的功能受到形状、数量和定位的变化的影响。控制线粒体网络的动力学,如生物发生和融合,或碎片化和分裂,最终会影响调节肌肉质量的信号通路。有规律的运动和健康的肌肉是人体代谢控制的重要参与者。事实上,久坐的生活方式对肌肉功能有害,是肥胖和糖尿病等代谢紊乱的主要原因之一。本文综述了过去几年在控制蛋白水解系统以及肌肉质量和功能丧失方面线粒体作用的快速进展。

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本文引用的文献

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Peroxisome proliferator-activated receptor gamma coactivator 1alpha or 1beta overexpression inhibits muscle protein degradation, induction of ubiquitin ligases, and disuse atrophy.过氧化物酶体增殖物激活受体γ共激活因子 1α或 1β过表达可抑制肌肉蛋白降解、泛素连接酶的诱导以及废用性萎缩。
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The Role of Mitophagy in Skeletal Muscle Damage and Regeneration.自噬在骨骼肌损伤与再生中的作用
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PGC-1alpha-mediated adaptations in skeletal muscle.
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Mitochondrial fission and remodelling contributes to muscle atrophy.线粒体分裂和重塑有助于肌肉萎缩。
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