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Increased mitochondrial Ca <sup>2+</sup> contributes to health decline with age and Duchene muscular dystrophy in <i>C. elegans</i>

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

2023The FASEB Journal28 citationsDOIOpen Access PDF

Abstract

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 2+ 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 2+ 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 2+ levels. Taken together, our results reveal that elevated resting mitochondrial Ca 2+ 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.

Topics & Concepts

SarcopeniaMuscular dystrophyMitochondrionMitophagyCaenorhabditis elegansSkeletal muscleBiologyDystrophyCalciumEndocrinologyInternal medicineCell biologyAnatomyMedicineBiochemistryGeneticsApoptosisGeneAutophagyMitochondrial Function and PathologyGenetics, Aging, and Longevity in Model OrganismsCoenzyme Q10 studies and effects
Increased mitochondrial Ca <sup>2+</sup> contributes to health decline with age and Duchene muscular dystrophy in <i>C. elegans</i> | Litcius