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神经元中的Ca(v)1 L型Ca2+通道信号复合物

Ca(v)1 L-type Ca2+ channel signaling complexes in neurons.

作者信息

Calin-Jageman Irina, Lee Amy

机构信息

Department of Pharmacology and Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

J Neurochem. 2008 May;105(3):573-83. doi: 10.1111/j.1471-4159.2008.05286.x. Epub 2008 Feb 7.

Abstract

Ca(v)1 L-type Ca2+ channels play crucial and diverse roles in the nervous system. The pre- and post-synaptic functions of Ca(v)1 channels not only depend on their intrinsic biophysical properties but also their dynamic regulation by a host of cellular influences. These include protein kinases and phosphatases, G-protein coupled receptors, scaffolding proteins, and Ca2+-binding proteins. The cytoplasmic domains of the main pore forming alpha(1) subunit of Ca(v)1 offer a number of binding sites for these modulators, permitting fast and localized regulation of Ca2+ entry. Through effects on Ca(v)1 gating, localization, and coupling to effectors, protein modulators are efficiently positioned to adjust Ca(v)1 Ca2+ signals that control neuronal excitability, synaptic plasticity, and gene expression.

摘要

Ca(v)1 L型钙离子通道在神经系统中发挥着至关重要且多样的作用。Ca(v)1通道的突触前和突触后功能不仅取决于其内在的生物物理特性,还取决于众多细胞影响因素对其的动态调节。这些因素包括蛋白激酶和磷酸酶、G蛋白偶联受体、支架蛋白和钙离子结合蛋白。Ca(v)1主要孔形成α(1)亚基的胞质结构域为这些调节剂提供了多个结合位点,从而允许对钙离子内流进行快速且局部的调节。通过对Ca(v)1门控、定位以及与效应器偶联的影响,蛋白调节剂能够有效地调节Ca(v)1钙离子信号,进而控制神经元兴奋性、突触可塑性和基因表达。

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