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线粒体钙含量增加会导致秀丽隐杆线虫随着年龄增长以及患杜氏肌营养不良症而出现健康状况下降。

Increased mitochondrial Ca contributes to health decline with age and Duchene muscular dystrophy in C. elegans.

作者信息

Higashitani Atsushi, Teranishi Mika, Nakagawa Yui, Itoh Yukou, Sudevan Surabhi, Szewczyk Nathaniel J, Kubota Yukihiko, Abe Takaaki, Kobayashi Takeshi

机构信息

Graduate School of Life Sciences, Tohoku University, Sendai, Japan.

Medical Research Council (MRC) Versus Arthritis, Centre for Musculoskeletal Ageing Research, Royal Derby Hospital, University of Nottingham, Derby, UK.

出版信息

FASEB J. 2023 Apr;37(4):e22851. doi: 10.1096/fj.202201489RR.

Abstract

Sarcopenia is a geriatric syndrome characterized by an age-related decline in skeletal muscle mass and strength. Here, we show that suppression of mitochondrial calcium uniporter (MCU)-mediated Ca influx into mitochondria in the body wall muscles of the nematode Caenorhabditis elegans improved the sarcopenic phenotypes, blunting movement and mitochondrial structural and functional decline with age. We found that normally aged muscle cells exhibited elevated resting mitochondrial Ca levels and increased mitophagy to eliminate damaged mitochondria. Similar to aging muscle, we found that suppressing MCU function in muscular dystrophy improved movement via reducing elevated resting mitochondrial Ca levels. Taken together, our results reveal that elevated resting mitochondrial Ca levels contribute to muscle decline with age and muscular dystrophy. Further, modulation of MCU activity may act as a potential pharmacological target in various conditions involving muscle loss.

摘要

肌肉减少症是一种老年综合征,其特征是骨骼肌质量和力量随年龄下降。在此,我们表明,抑制线虫秀丽隐杆线虫体壁肌肉中线粒体钙单向转运体(MCU)介导的钙流入线粒体可改善肌肉减少症表型,减轻随着年龄增长而出现的运动能力、线粒体结构和功能衰退。我们发现,正常衰老的肌肉细胞表现出静息线粒体钙水平升高以及线粒体自噬增加,以清除受损的线粒体。与衰老肌肉相似,我们发现,在肌肉营养不良中抑制MCU功能可通过降低升高的静息线粒体钙水平来改善运动能力。综上所述,我们的结果表明,静息线粒体钙水平升高会导致肌肉随年龄增长和肌肉营养不良而衰退。此外,调节MCU活性可能在各种涉及肌肉流失的情况下作为一种潜在的药理学靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/10946577/a207ba0b56be/FSB2-37-e22851-g004.jpg

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