Zhou Xiaoxu, Shentu Ping, Xu Yingke
Department of Biomedical Engineering, Key Laboratory for Biomedical Engineering of Ministry of Education, Zhejiang Provincial Key Laboratory of Cardio-Cerebral Vascular Detection Technology and Medicinal Effectiveness Appraisal, Zhejiang University, Hangzhou 310027, China.
J Diabetes Res. 2017;2017:1683678. doi: 10.1155/2017/1683678. Epub 2017 Apr 25.
Insulin increases glucose uptake and storage in muscle and adipose cells, which is accomplished through the mobilization of intracellular GLUT4 storage vesicles (GSVs) to the cell surface upon stimulation. Importantly, the dysfunction of insulin-regulated GLUT4 trafficking is strongly linked with peripheral insulin resistance and type 2 diabetes in human. The insulin signaling pathway, key signaling molecules involved, and precise trafficking itinerary of GSVs are largely identified. Understanding the interaction between insulin signaling molecules and key regulatory proteins that are involved in spatiotemporal regulation of GLUT4 vesicle exocytosis is of great importance to explain the pathogenesis of diabetes and may provide new potential therapeutic targets.
胰岛素可增加肌肉和脂肪细胞对葡萄糖的摄取与储存,这是通过刺激后将细胞内的GLUT4储存囊泡(GSV)转运至细胞表面来实现的。重要的是,胰岛素调节的GLUT4转运功能障碍与人类外周胰岛素抵抗及2型糖尿病密切相关。胰岛素信号通路、其中涉及的关键信号分子以及GSV精确的转运路径已基本明确。了解胰岛素信号分子与参与GLUT4囊泡胞吐时空调节的关键调节蛋白之间的相互作用,对于解释糖尿病的发病机制至关重要,并且可能提供新的潜在治疗靶点。