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anoctamin 2通道脑亚型中的细胞内环调节钙依赖性激活。

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

作者信息

Lee Dongsu, Lim Hocheol, Lee Jungryun, Ha Go Eun, No Kyoung Tai, Cheong Eunji

机构信息

Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Korea.

The Interdisciplinary Graduate Program in Integrative Biotechnology & Translational Medicine, Yonsei University, Incheon 21983, Korea.

出版信息

Exp Neurobiol. 2023 Jun 30;32(3):133-146. doi: 10.5607/en22045.

Abstract

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 Ca at relatively fast kinetics. In other brain regions, including the thalamus, ANO2 mediates activity-dependent spike frequency adaptations with low sensitivity to Ca at relatively slow kinetics. How this same channel can respond to a wide range of Ca levels remains unclear. We hypothesized that splice variants of ANO2 may contribute to its distinct Ca 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.

摘要

anoctamin 2(ANO2或TMEM16B)是一种钙激活氯离子通道(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可使动作电位宽度变窄,并以相对较快的动力学对钙高度敏感地降低突触后去极化。在包括丘脑在内的其他脑区,ANO2以相对较慢的动力学对钙低敏感地介导活动依赖性的峰频率适应。同一通道如何能对广泛的钙水平做出反应仍不清楚。我们推测ANO2的剪接变体可能导致其对钙的敏感性不同,从而其神经元功能也不同。我们在小鼠大脑中鉴定出两种ANO2亚型,并研究了它们的电生理特性:亚型1(由含有外显子1a、2、4和14的剪接变体编码)在海马体中表达,而亚型2(由含有外显子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,并且其钙依赖性激活电流比亚型1慢。计算模型显示,亚型1的第一个细胞内环的二级结构形成了一个从细胞质到钙结合位点的入口腔,该入口腔比亚型2中的相对更大。这种差异提供了结构证据,表明亚型2参与调节峰频率,而亚型1参与塑造动作电位的持续时间并减少突触后去极化。我们的研究突出了特定ANO2剪接变体在调节神经元功能中的作用和分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61b1/10327929/b01712808381/en-32-3-133-f1.jpg

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