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CBL/CAP 对于线粒体呼吸复合物 I 组装和肌肉细胞的生物能量效率是必需的。

CBL/CAP Is Essential for Mitochondria Respiration Complex I Assembly and Bioenergetics Efficiency in Muscle Cells.

机构信息

The Department of Cellular and Molecular Physiology, Institute of Translational Medicine, The University of Liverpool, Crown Street, Liverpool L69 3BX, UK.

Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.

出版信息

Int J Mol Sci. 2023 Feb 8;24(4):3399. doi: 10.3390/ijms24043399.

Abstract

CBL is rapidly phosphorylated upon insulin receptor activation. Mice whole body CBL depletion improved insulin sensitivity and glucose clearance; however, the precise mechanisms remain unknown. We depleted either CBL or its associated protein SORBS1/CAP independently in myocytes and assessed mitochondrial function and metabolism compared to control cells. CBL- and CAP-depleted cells showed increased mitochondrial mass with greater proton leak. Mitochondrial respiratory complex I activity and assembly into respirasomes were reduced. Proteome profiling revealed alterations in proteins involved in glycolysis and fatty acid degradation. Our findings demonstrate CBL/CAP pathway couples insulin signaling to efficient mitochondrial respiratory function and metabolism in muscle.

摘要

CBL 在胰岛素受体激活后迅速发生磷酸化。全身敲除 CBL 的小鼠改善了胰岛素敏感性和葡萄糖清除率;然而,确切的机制尚不清楚。我们在肌细胞中分别敲除 CBL 或其相关蛋白 SORBS1/CAP,并与对照细胞比较评估线粒体功能和代谢。CBL 和 CAP 敲除的细胞显示出更大的质子渗漏,线粒体质量增加。线粒体呼吸复合物 I 的活性和呼吸体组装减少。蛋白质组学分析显示,参与糖酵解和脂肪酸降解的蛋白质发生改变。我们的研究结果表明,CBL/CAP 途径将胰岛素信号与肌肉中有效的线粒体呼吸功能和代谢联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9cc/9964740/e914f7e139ab/ijms-24-03399-g001.jpg

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