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胰岛素通过激活TC10诱导磷脂酰肌醇-3-磷酸的形成。

Insulin induces phosphatidylinositol-3-phosphate formation through TC10 activation.

作者信息

Maffucci Tania, Brancaccio Anna, Piccolo Enza, Stein Robert C, Falasca Marco

机构信息

The Sackler Institute, University College London, 5 University Street, London WC1E 6JJ, UK.

出版信息

EMBO J. 2003 Aug 15;22(16):4178-89. doi: 10.1093/emboj/cdg402.

Abstract

Phosphatidylinositol-3-phosphate (PtdIns-3-P) is considered as a lipid constitutively present on endosomes; it does not seem to have a dynamic role in signalling. In contrast, phosphatidylinositol-3,4,5-trisphosphate (PtdIns-3,4,5-P(3)) plays a crucial role in different signalling pathways including translocation of the glucose transporter protein GLUT4 to the plasma membrane upon insulin receptor activation. GLUT4 translocation requires activation of two distinct pathways involving phosphatidylinositol 3-kinase (PI 3-K) and the small GTP-binding protein TC10, respectively. The contribution of each pathway remains to be elucidated. Here we show that insulin specifically induces the formation of PtdIns-3-P in insulin- responsive cells. The insulin-mediated formation of PtdIns-3-P occurs through the activation of TC10 at the lipid rafts subdomain of the plasma membrane. Exogenous PtdIns-3-P induces the plasma membrane translocation of both overexpressed and endogenous GLUT4. These data indicate that PtdIns-3-P is specifically produced downstream from insulin-mediated activation of TC10 to promote the plasma membrane translocation of GLUT4. These results give a new insight into the intracellular role of PtdIns-3-P and shed light on some aspects of insulin signalling so far not completely understood.

摘要

磷脂酰肌醇-3-磷酸(PtdIns-3-P)被认为是一种在内体上组成性存在的脂质;它似乎在信号传导中没有动态作用。相比之下,磷脂酰肌醇-3,4,5-三磷酸(PtdIns-3,4,5-P(3))在不同的信号通路中起着关键作用,包括胰岛素受体激活后葡萄糖转运蛋白GLUT4向质膜的转位。GLUT4转位需要分别激活涉及磷脂酰肌醇3-激酶(PI 3-K)和小GTP结合蛋白TC10的两条不同途径。每条途径的贡献仍有待阐明。在这里,我们表明胰岛素特异性地诱导胰岛素反应性细胞中PtdIns-3-P的形成。胰岛素介导的PtdIns-3-P形成是通过质膜脂筏亚结构域中TC10的激活而发生的。外源性PtdIns-3-P诱导过表达和内源性GLUT4向质膜转位。这些数据表明,PtdIns-3-P是在胰岛素介导的TC10激活下游特异性产生的,以促进GLUT4向质膜的转位。这些结果为PtdIns-3-P的细胞内作用提供了新的见解,并揭示了迄今为止尚未完全理解的胰岛素信号传导的一些方面。

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