过剩4
葡萄糖转运蛋白
胰岛素
胞吐
小泡
葡萄糖摄取
胰岛素抵抗
葡萄糖稳态
生物
胰岛素受体
细胞生物学
内科学
内分泌学
生物化学
医学
分泌物
膜
作者
Dara E. Leto,Alan R. Saltiel
摘要
Despite daily fasting and feeding, plasma glucose levels are normally maintained within a narrow range owing to the hormones insulin and glucagon. Insulin increases glucose uptake into fat and muscle cells through the regulated trafficking of vesicles that contain glucose transporter type 4 (GLUT4). New insights into insulin signalling reveal that phosphorylation events initiated by the insulin receptor regulate key GLUT4 trafficking proteins, including small GTPases, tethering complexes and the vesicle fusion machinery. These proteins, in turn, control GLUT4 movement through the endosomal system, formation and retention of specialized GLUT4 storage vesicles and targeted exocytosis of these vesicles. Understanding these processes may help to explain the development of insulin resistance in type 2 diabetes and provide new potential therapeutic targets.
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