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哺乳动物中枢神经元中GIRK通道的定位与靶向

Localization and Targeting of GIRK Channels in Mammalian Central Neurons.

作者信息

Luján Rafael, Aguado Carolina

机构信息

Instituto de Investigación en Discapacidades Neurológicas (IDINE), Departamento de Ciencias Médicas, Facultad de Medicina, Universidad Castilla-La Mancha, Campus Biosanitario, Albacete, Spain.

Instituto de Investigación en Discapacidades Neurológicas (IDINE), Departamento de Ciencias Médicas, Facultad de Medicina, Universidad Castilla-La Mancha, Campus Biosanitario, Albacete, Spain.

出版信息

Int Rev Neurobiol. 2015;123:161-200. doi: 10.1016/bs.irn.2015.05.009.

Abstract

G protein-gated inwardly rectifying K(+) (GIRK/K(ir)3) channels are critical to brain function. They hyperpolarize neurons in response to activation of different G protein-coupled receptors, reducing cell excitability. Molecular cloning has revealed four distinct mammalian genes (GIRK1-4), which, with the exception of GIRK4, are broadly expressed in the central nervous system (CNS) and have been implicated in a variety of neurological disorders. Although the molecular structure and composition of GIRK channels are key determinants of their biophysical properties, their cellular and subcellular localization patterns and densities on the neuronal surface are just as important to nerve function. Current data obtained with high-resolution quantitative localization techniques reveal complex, subcellular compartment-specific distribution patterns of GIRK channel subunits. Recent efforts have focused on determining the associated proteins that form macromolecular complexes with GIRK channels. Demonstration of the precise subcellular compartmentalization of GIRK channels and their associated proteins represents a crucial step in understanding the contribution of these channels to specific aspects of neuronal function under both physiological and pathological conditions. Here, we present an overview of studies aimed at determining the cellular and subcellular localization of GIRK channel subunits in mammalian brain neurons and discuss implications for neuronal physiology.

摘要

G蛋白门控内向整流钾离子(GIRK/K(ir)3)通道对脑功能至关重要。它们在不同G蛋白偶联受体激活时使神经元超极化,降低细胞兴奋性。分子克隆已揭示出四个不同的哺乳动物基因(GIRK1 - 4),除GIRK4外,这些基因在中枢神经系统(CNS)中广泛表达,并与多种神经疾病有关。尽管GIRK通道的分子结构和组成是其生物物理特性的关键决定因素,但其在细胞和亚细胞水平的定位模式以及在神经元表面的密度对神经功能同样重要。利用高分辨率定量定位技术获得的当前数据揭示了GIRK通道亚基复杂的、亚细胞区室特异性分布模式。最近的研究致力于确定与GIRK通道形成大分子复合物的相关蛋白。证明GIRK通道及其相关蛋白精确的亚细胞区室化是理解这些通道在生理和病理条件下对神经元功能特定方面贡献的关键一步。在此,我们概述旨在确定哺乳动物脑神经元中GIRK通道亚基细胞和亚细胞定位的研究,并讨论其对神经元生理学的意义。

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