DEFINING THE MOLECULAR COMPONENTS OF GLUT4 TRANSLOCATION

定义 GLUT4 易位的分子成分

• 批准号: 6178057
• 负责人: Bentley Cheatham
• 金额: $ 14.64万
• 依托单位: JOSLIN DIABETES CENTER
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-04-26 至 2002-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6178057
• 关键词: adipocytes; binding proteins; biological signal transduction; cell line; chimeric proteins; exocytosis; glucose metabolism; glucose transport; glucose transporter; guanine nucleotide binding protein; hormone regulation /control mechanism; immunoprecipitation; insulin; intracellular transport; membrane fusion; membrane proteins; molecular cloning; mutant; protein protein interaction; protein purification; synthetic peptide; vesicle /vacuole; western blottings

In adipose tissue and skeletal muscle insulin induces the translocation o f GLUT4-containing vesicles to the ell surface resulting in an increase in glucose uptake. The mechanism of GLUT4 translocation is poorly understood. Recently several proteins involved in regulated exocytosis in neural and neuroendocrine tissues have been shown to be expressed in insulin-sensitive tissues. These proteins are components of the SNARE complex. In addition, members of the RAB family of small GTP-binding proteins that are involved in regulated endocytosis/exocytosis are also present in adipocytes and skeletal muscle. While these proteins have been implicated in insulin-regulated GLUT4 translocation no functional role has been determined. However, we have recently established that SNARE- complex proteins and specific members of the Rab family are necessary components in the GLUT4 translocation machinery. We have also identified a potentially novel protein that interacts with Rabs in adipocytes in an insulin-regulated manner. It is the purpose of this proposal to extend our preliminary observations to include a more detailed biochemical and cell biological analysis of these molecules. These studies will include experiments designed to investigate the specificity of protein-protein interactions between the SNARE proteins and their regulation by insulin, identification of other novel Rab-interacting proteins and pursuit of their molecular cloning. Data from these studies will allow us to define a more contemporary model of insulin-regulated glucose uptake.

在脂肪组织和骨骼肌中，胰岛素诱导移位 O含有GLUT4的囊泡进入细胞表面，导致 葡萄糖摄取增加。GLUT4易位机制的研究进展 人们对此知之甚少。最近参与调控的几种蛋白质 神经和神经内分泌组织中的胞吐作用已被证明 在胰岛素敏感组织中表达。这些蛋白质是 诱捕复合体的组成部分。此外，该委员会的成员 Rab家族的小GTP结合蛋白，参与 调节的内吞/胞吐作用也存在于脂肪细胞和 骨骼肌。虽然这些蛋白质被认为与 胰岛素调节的GLUT4易位没有功能作用 下定决心。然而，我们最近确定了陷阱-- Rab家族的复杂蛋白质和特定成员是 GLUT4转位机制中的必要组件。我们 还发现了一种潜在的新型蛋白质，它可以与 RABS以胰岛素调节的方式在脂肪细胞中表达。这就是目的 将我们的初步观察扩大到包括 更详细的生化和细胞生物学分析 分子。这些研究将包括旨在 研究蛋白质-蛋白质相互作用的特异性 SNARE蛋白及其受胰岛素的调节，鉴定 其他新的Rab相互作用蛋白及其分子研究进展 克隆。来自这些研究的数据将使我们能够定义更多 胰岛素调节葡萄糖摄取的当代模型。