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