脑内异辛胺2通道异构体的细胞内环调节钙依赖性激活。

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Dongsu Lee, Hocheol Lim, Jungryun Lee, Go Eun Ha, Kyoung Tai No, Eunji Cheong
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引用次数: 0

摘要

Anoctamin 2 (ANO2或TMEM16B)是一种钙激活的氯离子通道(CaCC),在整个中枢神经系统的神经元中发挥着多种作用。在海马神经元中,ANO2缩小动作电位宽度,减少突触后去极化,对Ca2+具有较高的敏感性,动力学相对较快。在包括丘脑在内的其他大脑区域,ANO2介导活动依赖的尖峰频率适应,对Ca2+的敏感性较低,动力学相对较慢。这个相同的通道如何对大范围的Ca2+水平作出反应尚不清楚。我们假设ANO2的剪接变体可能有助于其独特的Ca2+敏感性,从而其不同的神经元功能。我们鉴定了在小鼠大脑中表达的两种ANO2异构体,并检查了它们的电生理特性:异构体1(由外显子1a、2、4和14的剪接变体编码)在海马中表达,而异构体2(由外显子1a、2和4的剪接变体编码)在整个大脑中广泛表达,包括在皮层和丘脑中,并且具有比异构体1更慢的钙依赖性激活电流。计算模型显示,同型异构体1的第一个胞内环的二级结构形成了一个相对于同型异构体2的更大的从细胞质到钙结合位点的入口腔。这种差异提供了结构上的证据,表明同种异构体2参与调节尖峰频率,而同种异构体1参与塑造动作电位的持续时间和减少突触后去极化。我们的研究强调了特定的ANO2剪接变体在调节神经元功能中的作用和分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intracellular Loop in the Brain Isoforms of Anoctamin 2 Channels Regulates Calcium-dependent Activation.

Intracellular Loop in the Brain Isoforms of Anoctamin 2 Channels Regulates Calcium-dependent Activation.

Intracellular Loop in the Brain Isoforms of Anoctamin 2 Channels Regulates Calcium-dependent Activation.

Intracellular Loop in the Brain Isoforms of Anoctamin 2 Channels Regulates Calcium-dependent Activation.

Anoctamin 2 (ANO2 or TMEM16B), a calcium-activated chloride channel (CaCC), performs diverse roles in neurons throughout the central nervous system. In hippocampal neurons, ANO2 narrows action potential width and reduces postsynaptic depolarization with high sensitivity to Ca2+ at relatively fast kinetics. In other brain regions, including the thalamus, ANO2 mediates activity-dependent spike frequency adaptations with low sensitivity to Ca2+ at relatively slow kinetics. How this same channel can respond to a wide range of Ca2+ levels remains unclear. We hypothesized that splice variants of ANO2 may contribute to its distinct Ca2+ sensitivity, and thus its diverse neuronal functions. We identified two ANO2 isoforms expressed in mouse brains and examined their electrophysiological properties: isoform 1 (encoded by splice variants with exons 1a, 2, 4, and 14) was expressed in the hippocampus, while isoform 2 (encoded by splice variants with exons 1a, 2, and 4) was broadly expressed throughout the brain, including in the cortex and thalamus, and had a slower calcium-dependent activation current than isoform 1. Computational modeling revealed that the secondary structure of the first intracellular loop of isoform 1 forms an entrance cavity to the calcium-binding site from the cytosol that is relatively larger than that in isoform 2. This difference provides structural evidence that isoform 2 is involved in accommodating spike frequency, while isoform 1 is involved in shaping the duration of an action potential and decreasing postsynaptic depolarization. Our study highlights the roles and molecular mechanisms of specific ANO2 splice variants in modulating neuronal functions.

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来源期刊
Experimental Neurobiology
Experimental Neurobiology Neuroscience-Cellular and Molecular Neuroscience
CiteScore
4.30
自引率
4.20%
发文量
29
期刊介绍: Experimental Neurobiology is an international forum for interdisciplinary investigations of the nervous system. The journal aims to publish papers that present novel observations in all fields of neuroscience, encompassing cellular & molecular neuroscience, development/differentiation/plasticity, neurobiology of disease, systems/cognitive/behavioral neuroscience, drug development & industrial application, brain-machine interface, methodologies/tools, and clinical neuroscience. It should be of interest to a broad scientific audience working on the biochemical, molecular biological, cell biological, pharmacological, physiological, psychophysical, clinical, anatomical, cognitive, and biotechnological aspects of neuroscience. The journal publishes both original research articles and review articles. Experimental Neurobiology is an open access, peer-reviewed online journal. The journal is published jointly by The Korean Society for Brain and Neural Sciences & The Korean Society for Neurodegenerative Disease.
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