Uniporter公司
生物能学
线粒体
骨骼肌
氧化磷酸化
钙
细胞生物学
化学
钙代谢
心肌细胞
肌肉收缩
生物
生物化学
内分泌学
胞浆
有机化学
酶
作者
Bárbara Román,Yusuf Mastoor,Yingfan Zhang,D. Gross,Danielle Springer,Chengyu Liu,Brian Glancy,Elizabeth Murphy
摘要
Abstract Mitochondrial calcium concentration ([Ca 2+ ] m ) plays an essential role in bioenergetics, and loss of [Ca 2+ ] m homeostasis can trigger diseases and cell death in numerous cell types. Ca 2+ uptake into mitochondria occurs via the mitochondrial Ca 2+ uniporter (MCU), which is regulated by three mitochondrial Ca 2+ uptake (MICU) proteins localized in the intermembrane space, MICU1, 2, and 3. We generated a mouse model of systemic MICU3 ablation and examined its physiological role in skeletal muscle. We found that loss of MICU3 led to impaired exercise capacity. When the muscles were directly stimulated there was a decrease in time to fatigue. MICU3 ablation significantly increased the maximal force of the KO muscle and altered fibre type composition with an increase in the ratio of type IIb (low oxidative capacity) to type IIa (high oxidative capacity) fibres. Furthermore, MICU3‐KO mitochondria have reduced uptake of Ca 2+ and increased phosphorylation of pyruvate dehydrogenase, indicating that KO animals contain less Ca 2+ in their mitochondria. Skeletal muscle from MICU3‐KO mice exhibited lower net oxidation of NADH during electrically stimulated muscle contraction compared with wild‐type. These data demonstrate that MICU3 plays a role in skeletal muscle physiology by setting the proper threshold for mitochondrial Ca 2+ uptake, which is important for matching energy demand and supply in muscle. image Key points Mitochondrial calcium uptake is an important regulator of bioenergetics and cell death and is regulated by the mitochondrial calcium uniporter (MCU) and three calcium sensitive regulatory proteins (MICU1, 2 and 3). Loss of MICU3 leads to impaired exercise capacity and decreased time to skeletal muscle fatigue. Skeletal muscle from MICU3‐KO mice exhibits a net oxidation of NADH during electrically stimulated muscle contractions, suggesting that MICU3 plays a role in skeletal muscle physiology by matching energy demand and supply.
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