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胰岛素信号传导在质膜激活的融合步骤中与GLUT4的囊泡运输相遇。

Insulin signaling meets vesicle traffic of GLUT4 at a plasma-membrane-activated fusion step.

作者信息

Koumanov Françoise, Jin Bo, Yang Jing, Holman Geoffrey D

机构信息

Department of Biology and Biochemistry, University of Bath, UK.

出版信息

Cell Metab. 2005 Sep;2(3):179-89. doi: 10.1016/j.cmet.2005.08.007.

Abstract

A hypothesis that accounts for most of the available literature on insulin-stimulated GLUT4 translocation is that insulin action controls the access of GLUT4 vesicles to a constitutively active plasma-membrane fusion process. However, using an in vitro fusion assay, we show here that fusion is not constitutively active. Instead, the rate of fusion activity is stimulated 8-fold by insulin. Both the magnitude and time course of stimulated in vitro fusion recapitulate the cellular insulin response. Fusion is cell cytoplasm and SNARE dependent but does not require cell cytoskeleton. Furthermore, insulin activation of the plasma-membrane fraction of the fusion reaction is the essential step in regulation. Akt from the cytoplasm fraction is required for fusion. However, the participation of Akt in the stimulation of in vitro fusion is dependent on its in vitro recruitment onto the insulin-activated plasma membrane.

摘要

一个能够解释大部分关于胰岛素刺激的GLUT4转位现有文献的假说认为,胰岛素作用控制着GLUT4囊泡进入组成型活性的质膜融合过程。然而,我们在此利用体外融合试验表明,融合并非组成型活性的。相反,胰岛素可将融合活性速率提高8倍。体外融合刺激的幅度和时间进程都重现了细胞对胰岛素的反应。融合依赖于细胞质和SNARE,但不需要细胞骨架。此外,融合反应中质膜部分的胰岛素激活是调控的关键步骤。融合需要细胞质部分的Akt。然而,Akt参与体外融合的刺激取决于其在体外被募集到胰岛素激活的质膜上。

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