Extracellular protons enable activation of the calcium‐dependent chloride channel TMEM16A

S. Cruz-Rangel, J. J. Jesús-Pérez, I. Aréchiga-Figueroa, Aldo A. Rodríguez-Menchaca, P. Pérez-Cornejo, H. Hartzell, J. Arreola
{"title":"Extracellular protons enable activation of the calcium‐dependent chloride channel TMEM16A","authors":"S. Cruz-Rangel, J. J. Jesús-Pérez, I. Aréchiga-Figueroa, Aldo A. Rodríguez-Menchaca, P. Pérez-Cornejo, H. Hartzell, J. Arreola","doi":"10.1113/JP273111","DOIUrl":null,"url":null,"abstract":"The calcium‐activated chloride channel TMEM16A provides a pathway for chloride ion movements that are key in preventing polyspermy, allowing fluid secretion, controlling blood pressure, and enabling gastrointestinal activity. TMEM16A is opened by voltage‐dependent calcium binding and regulated by permeant anions and intracellular protons. Here we show that a low proton concentration reduces TMEM16A activity while maximum activation is obtained when the external proton concentration is high. In addition, protonation conditions determine the open probability of TMEM16A without changing its calcium sensitivity. External glutamic acid 623 (E623) is key for TMEM16A's ability to respond to external protons. At physiological pH, E623 is un‐protonated and TMEM16A is activated when intracellular calcium increases; however, under acidic conditions E623 is partially protonated and works synergistically with intracellular calcium to activate the channel. These findings are critical for understanding physiological and pathological processes that involve changes in pH and chloride flux via TMEM16A.","PeriodicalId":22512,"journal":{"name":"The Japanese journal of physiology","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"24","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Japanese journal of physiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1113/JP273111","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 24

Abstract

The calcium‐activated chloride channel TMEM16A provides a pathway for chloride ion movements that are key in preventing polyspermy, allowing fluid secretion, controlling blood pressure, and enabling gastrointestinal activity. TMEM16A is opened by voltage‐dependent calcium binding and regulated by permeant anions and intracellular protons. Here we show that a low proton concentration reduces TMEM16A activity while maximum activation is obtained when the external proton concentration is high. In addition, protonation conditions determine the open probability of TMEM16A without changing its calcium sensitivity. External glutamic acid 623 (E623) is key for TMEM16A's ability to respond to external protons. At physiological pH, E623 is un‐protonated and TMEM16A is activated when intracellular calcium increases; however, under acidic conditions E623 is partially protonated and works synergistically with intracellular calcium to activate the channel. These findings are critical for understanding physiological and pathological processes that involve changes in pH and chloride flux via TMEM16A.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
细胞外质子能够激活钙依赖性氯离子通道TMEM16A
钙激活的氯离子通道TMEM16A提供了氯离子运动的途径,这是防止多精子、允许液体分泌、控制血压和促进胃肠道活动的关键。TMEM16A通过电压依赖性钙结合打开,并通过渗透阴离子和细胞内质子调节。在这里,我们发现低质子浓度会降低TMEM16A的活性,而当外部质子浓度高时,TMEM16A的活性达到最大。此外,质子化条件决定了TMEM16A在不改变其钙敏感性的情况下的打开概率。外部谷氨酸623 (E623)是TMEM16A响应外部质子能力的关键。在生理pH下,当细胞内钙增加时,E623是非质子化的,TMEM16A被激活;然而,在酸性条件下,E623部分质子化,并与细胞内钙协同作用激活通道。这些发现对于理解通过TMEM16A改变pH和氯化物通量的生理和病理过程至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The substantia nigra modulates proximal colon tone and motility in a vagally-dependent manner in the rat. Mechanisms of Hebbian‐like plasticity in the ventral premotor – primary motor network Maternal obesity: influencing the heart right from the start Motor unit dysregulation following 15 days of unilateral lower limb immobilisation Back to the beginning: can we stop brain injury before it starts?
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1