DEG/ENaC Ion Channels in the Function of the Nervous System: From Worm to Man

门控 上皮钠通道 细胞外 离子通道 神经系统 生物物理学 酸敏离子通道 化学 细胞生物学 生物 生物化学 神经科学 受体 有机化学
作者
Laura Bianchi
出处
期刊:Advances in Experimental Medicine and Biology [Springer Nature]
卷期号:: 165-192 被引量:5
标识
DOI:10.1007/978-981-16-4254-8_9
摘要

DEG/ENaC channels are voltage-independent Na+/Ca2+ channels that are conserved across species and are expressed in many different cell types and tissues, where they contribute to a wide array of physiological functions from transepithelial Na+ transport, to sensory perception, and learning and memory. In this chapter, we focus on the members of this family that are expressed in the nervous system, grouping them based on their function. Structurally, DEG/ENaC channels are trimers formed by either identical or homologous subunits, each one protruding from the plasma membrane like a clenched hand. Crystallographic studies on chicken ASIC1a in the closed, inactivated, and open states revealed important details about the gating and permeation properties of these channels, and overall they show that the extracellular domain of the channel undergoes large conformational changes during gating. The vast majority of the channel's extracellular domain is conserved across different members and species; however, key changes including the insertion of extra loops near the finger and palm domains most likely confers gating specificity. Indeed, DEG/ENaC channels are gated by a wide range of stimuli, including mechanical forces, protons, and peptides, owing to the wide array of physiological functions they serve. Interestingly, DEG/ENaC channels are not only expressed in neurons but also in glia. Work in C. elegans is now beginning to shed new light on the role of glial DEG/ENaC in the function of the nervous system and suggests that they may be implicated in controlling ionic concentrations in the extracellular microenvironment. Finally, DEG/ENaC channels can become toxic and cause neuronal death when they are hyperactivated by genetic mutations or prolonged acidosis causing them to contribute to neuronal demise in stroke and ischemia. Taken together, molecular, structural, and behavioral work on DEG/ENaC channels expressed in the nervous system of different species highlights the crucial role of these channels in neuronal function. These data place DEG/ENaC channels in an excellent position for being considered as drug targets for the treatment of several neurological conditions and disorders from pain to epilepsy and ischemia.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
夕荀发布了新的文献求助10
1秒前
123完成签到 ,获得积分10
1秒前
社会主义接班人完成签到 ,获得积分10
2秒前
上官完成签到 ,获得积分10
3秒前
忧郁紫翠发布了新的文献求助10
3秒前
4秒前
ykiiii发布了新的文献求助10
4秒前
keke完成签到,获得积分10
5秒前
我是老大应助Starry采纳,获得10
5秒前
6秒前
8秒前
一口娴蛋黄完成签到 ,获得积分10
8秒前
CodeCraft应助英俊qiang采纳,获得10
8秒前
Fjun发布了新的文献求助10
9秒前
春词弥弥发布了新的文献求助10
9秒前
田様应助YMP采纳,获得10
10秒前
科研通AI6.4应助飘逸鸵鸟采纳,获得10
11秒前
12302发布了新的文献求助20
11秒前
12秒前
阿云完成签到,获得积分10
12秒前
夕荀完成签到,获得积分10
13秒前
13秒前
Zoe发布了新的文献求助10
13秒前
wanci应助飞快的诗槐采纳,获得20
14秒前
大胆的忆安完成签到 ,获得积分10
14秒前
风陌子若完成签到,获得积分10
14秒前
16秒前
慕青应助许飞采纳,获得10
17秒前
小马甲应助科研通管家采纳,获得10
17秒前
NexusExplorer应助科研通管家采纳,获得10
17秒前
wanci应助科研通管家采纳,获得10
17秒前
隐形曼青应助科研通管家采纳,获得10
17秒前
Ava应助科研通管家采纳,获得30
17秒前
FashionBoy应助科研通管家采纳,获得10
17秒前
脑洞疼应助科研通管家采纳,获得10
17秒前
CodeCraft应助科研通管家采纳,获得10
18秒前
8R60d8应助科研通管家采纳,获得10
18秒前
18秒前
852应助科研通管家采纳,获得10
18秒前
852应助双子土豆泥采纳,获得10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Real Analysis: Theory of Measure and Integration (3rd Edition) Epub版 1200
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
卤化钙钛矿人工突触的研究 1000
Engineering for calcareous sediments : proceedings of the International Conference on Calcareous Sediments, Perth 15-18 March 1988 / edited by R.J. Jewell, D.C. Andrews 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6260866
求助须知:如何正确求助?哪些是违规求助? 8082760
关于积分的说明 16888828
捐赠科研通 5332135
什么是DOI,文献DOI怎么找? 2838361
邀请新用户注册赠送积分活动 1815794
关于科研通互助平台的介绍 1669511