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GLUT4 胞吐作用。

GLUT4 exocytosis.

机构信息

Diabetes and Obesity Program, Garvan Institute of Medical Research, Sydney, New South Wales 2010, Australia.

出版信息

J Cell Sci. 2011 Dec 15;124(Pt 24):4147-59. doi: 10.1242/jcs.097063.

Abstract

GLUT4 is an insulin-regulated glucose transporter that is responsible for insulin-regulated glucose uptake into fat and muscle cells. In the absence of insulin, GLUT4 is mainly found in intracellular vesicles referred to as GLUT4 storage vesicles (GSVs). Here, we summarise evidence for the existence of these specific vesicles, how they are sequestered inside the cell and how they undergo exocytosis in the presence of insulin. In response to insulin stimulation, GSVs fuse with the plasma membrane in a rapid burst and in the continued presence of insulin GLUT4 molecules are internalised and recycled back to the plasma membrane in vesicles that are distinct from GSVs and probably of endosomal origin. In this Commentary we discuss evidence that this delivery process is tightly regulated and involves numerous molecules. Key components include the actin cytoskeleton, myosin motors, several Rab GTPases, the exocyst, SNARE proteins and SNARE regulators. Each step in this process is carefully orchestrated in a sequential and coupled manner and we are beginning to dissect key nodes within this network that determine vesicle-membrane fusion in response to insulin. This regulatory process clearly involves the Ser/Thr kinase AKT and the exquisite manner in which this single metabolic process is regulated makes it a likely target for lesions that might contribute to metabolic disease.

摘要

GLUT4 是一种胰岛素调节的葡萄糖转运蛋白,负责将胰岛素调节的葡萄糖摄取到脂肪和肌肉细胞中。在没有胰岛素的情况下,GLUT4 主要存在于称为 GLUT4 储存小泡(GSV)的细胞内小泡中。在这里,我们总结了这些特定小泡存在的证据,它们如何在细胞内被隔离,以及在胰岛素存在的情况下如何进行胞吐作用。在胰岛素刺激下,GSV 与质膜快速融合,并且在胰岛素持续存在的情况下,GLUT4 分子被内化并通过与 GSV 不同且可能来源于内体的小泡循环回到质膜。在这篇评论中,我们讨论了证据表明该递呈过程受到严格调控,涉及许多分子。关键成分包括肌动球蛋白细胞骨架、肌球蛋白马达、几种 Rab GTPases、外核体、SNARE 蛋白和 SNARE 调节剂。这个过程中的每一步都以顺序和耦合的方式精心协调,我们开始剖析这个网络中的关键节点,这些节点决定了胰岛素刺激下的囊泡-膜融合。这个调节过程显然涉及丝氨酸/苏氨酸激酶 AKT,而这种单一代谢过程的精确调节使其成为可能导致代谢疾病的病变的潜在靶点。

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