LaBarge Samuel, Migdal Christopher, Schenk Simon
Department of Orthopaedic Surgery, University of California, San Diego, CA, 92093, USA.
Biomedical Sciences Graduate Program, University of California, San Diego, CA, 92093, USA.
Mol Cells. 2015 Apr;38(4):297-303. doi: 10.14348/molcells.2015.0020. Epub 2015 Mar 31.
Skeletal muscle insulin resistance, which increases the risk for developing various metabolic diseases, including type 2 diabetes, is a common metabolic disorder in obesity and aging. If potential treatments are to be developed to treat insulin resistance, then it is important to fully understand insulin signaling and glucose metabolism. While recent large-scale "omics" studies have revealed the acetylome to be comparable in size to the phosphorylome, the acetylation of insulin signaling proteins and its functional relevance to insulin-stimulated glucose transport and glucose metabolism is not fully understood. In this Mini Review we discuss the acetylation status of proteins involved in the insulin signaling pathway and review their potential effect on, and relevance to, insulin action in skeletal muscle.
骨骼肌胰岛素抵抗是肥胖和衰老中常见的代谢紊乱,它会增加患包括2型糖尿病在内的各种代谢疾病的风险。如果要开发潜在的治疗方法来治疗胰岛素抵抗,那么充分了解胰岛素信号传导和葡萄糖代谢就很重要。虽然最近的大规模“组学”研究表明乙酰化蛋白质组的规模与磷酸化蛋白质组相当,但胰岛素信号蛋白的乙酰化及其与胰岛素刺激的葡萄糖转运和葡萄糖代谢的功能相关性尚未完全了解。在本综述中,我们讨论了胰岛素信号通路中相关蛋白质的乙酰化状态,并综述了它们对骨骼肌胰岛素作用的潜在影响及其相关性。