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GABAB受体的分子多样性、转运及亚细胞定位

Molecular diversity, trafficking and subcellular localization of GABAB receptors.

作者信息

Bettler Bernhard, Tiao Jim Yu-Hsiang

机构信息

Institute of Physiology, Department of Clinical-Biological Sciences, Pharmazentrum, Klingelbergstrasse 50-70, University of Basel, CH-4056 Basel, Switzerland.

出版信息

Pharmacol Ther. 2006 Jun;110(3):533-43. doi: 10.1016/j.pharmthera.2006.03.006. Epub 2006 Apr 27.

Abstract

GABAB receptors are the G-protein coupled receptors for the main inhibitory neurotransmitter in the brain, gamma-aminobutyric acid (GABA). While native studies predicted pharmacologically distinct GABAB receptor subtypes, molecular studies failed to identify the expected receptor varieties. Mouse genetic experiments therefore addressed whether the cloned receptors can account for the classical electrophysiological, biochemical and behavioral GABAB responses or whether additional receptors exist. Among G-protein coupled receptors, GABAB receptors are unique in that they require 2 distinct subunits for functioning. This atypical receptor structure triggered a large body of work that investigated the regulation of receptor assembly and trafficking. With the availability of molecular tools, substantial progress was also made in the analysis of the receptor protein distribution in neuronal compartments. Here, we review recent studies that shed light on the molecular diversity, the subcellular distribution and the cell surface dynamics of GABAB receptors.

摘要

GABAB受体是大脑中主要抑制性神经递质γ-氨基丁酸(GABA)的G蛋白偶联受体。虽然早期研究预测了药理学上不同的GABAB受体亚型,但分子研究未能识别出预期的受体种类。因此,小鼠遗传学实验探讨了克隆的受体是否能解释经典的电生理、生化和行为学GABAB反应,或者是否存在其他受体。在G蛋白偶联受体中,GABAB受体的独特之处在于它们需要两个不同的亚基才能发挥作用。这种非典型的受体结构引发了大量研究受体组装和运输调控的工作。随着分子工具的出现,在分析受体蛋白在神经元区室中的分布方面也取得了实质性进展。在此,我们综述了最近的研究,这些研究揭示了GABAB受体的分子多样性、亚细胞分布和细胞表面动力学。

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