细胞内第二信使介导a7- nachr诱导的调节的作用

Mengzhen Wang, Shan Zhao, Yudan Zhang, W. Liu, Jie Wu
{"title":"细胞内第二信使介导a7- nachr诱导的调节的作用","authors":"Mengzhen Wang, Shan Zhao, Yudan Zhang, W. Liu, Jie Wu","doi":"10.59566/ijbs.2022.18005","DOIUrl":null,"url":null,"abstract":"Nicotinic acetylcholine receptors (nAChRs) are the members of the cys-loop ligandgated ion channel superfamily. They are cation-selective membrane proteins with a homopentameric or heteropentameric structure. The α7 subtype of nAChR (α7-nAChR) belongs to the classical homopentameric structure with the characteristics of relatively low affinity to agonists and high permeability to Ca2+. α7-nAChR plays an important role in modulating learning and memory, cognition, anti-inflammatory, growth and development, and other processes. There are many possible mechanisms underlying α7-nAChR-mediated modulations, including opening the high Ca2+ permeable channels, regulating presynaptic neurotransmitter release, and altering intracellular second messenger-mediated signaling pathways. Here, we summarize the signal pathways associated with α7-nAChR activation involving nucleotides, ions, lipids, and gas molecules. This article provides insights into α7-nAChR-mediated modulations through intracellular signaling systems and helps to understand the α7-nAChR-associated pathogenesis and therapeutics of a variety of diseases and disorders.","PeriodicalId":13852,"journal":{"name":"International Journal of Biomedical Science : IJBS","volume":"231 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Roles of Intracellular Second Messengers in Mediation of a7-nAChR-induced Modulations\",\"authors\":\"Mengzhen Wang, Shan Zhao, Yudan Zhang, W. Liu, Jie Wu\",\"doi\":\"10.59566/ijbs.2022.18005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Nicotinic acetylcholine receptors (nAChRs) are the members of the cys-loop ligandgated ion channel superfamily. They are cation-selective membrane proteins with a homopentameric or heteropentameric structure. The α7 subtype of nAChR (α7-nAChR) belongs to the classical homopentameric structure with the characteristics of relatively low affinity to agonists and high permeability to Ca2+. α7-nAChR plays an important role in modulating learning and memory, cognition, anti-inflammatory, growth and development, and other processes. There are many possible mechanisms underlying α7-nAChR-mediated modulations, including opening the high Ca2+ permeable channels, regulating presynaptic neurotransmitter release, and altering intracellular second messenger-mediated signaling pathways. Here, we summarize the signal pathways associated with α7-nAChR activation involving nucleotides, ions, lipids, and gas molecules. This article provides insights into α7-nAChR-mediated modulations through intracellular signaling systems and helps to understand the α7-nAChR-associated pathogenesis and therapeutics of a variety of diseases and disorders.\",\"PeriodicalId\":13852,\"journal\":{\"name\":\"International Journal of Biomedical Science : IJBS\",\"volume\":\"231 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-03-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Biomedical Science : IJBS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.59566/ijbs.2022.18005\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Biomedical Science : IJBS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59566/ijbs.2022.18005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

烟碱乙酰胆碱受体(Nicotinic acetylcholine receptor, nAChRs)是cys环配体离子通道超家族的成员。它们是具有同戊二聚体或异戊二聚体结构的阳离子选择性膜蛋白。nAChR α7亚型(α7-nAChR)属于经典的同戊二聚体结构,对激动剂的亲和力相对较低,对Ca2+的渗透性较高。α7-nAChR在调节学习记忆、认知、抗炎、生长发育等过程中发挥重要作用。α7- nachr介导的调节有许多可能的机制,包括打开高Ca2+可渗透通道,调节突触前神经递质释放,改变细胞内第二信使介导的信号通路。在这里,我们总结了与α7-nAChR激活相关的信号通路,包括核苷酸、离子、脂质和气体分子。本文提供了α7- nachr通过细胞内信号系统介导的调节,并有助于了解α7- nachr相关的多种疾病和障碍的发病机制和治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Roles of Intracellular Second Messengers in Mediation of a7-nAChR-induced Modulations
Nicotinic acetylcholine receptors (nAChRs) are the members of the cys-loop ligandgated ion channel superfamily. They are cation-selective membrane proteins with a homopentameric or heteropentameric structure. The α7 subtype of nAChR (α7-nAChR) belongs to the classical homopentameric structure with the characteristics of relatively low affinity to agonists and high permeability to Ca2+. α7-nAChR plays an important role in modulating learning and memory, cognition, anti-inflammatory, growth and development, and other processes. There are many possible mechanisms underlying α7-nAChR-mediated modulations, including opening the high Ca2+ permeable channels, regulating presynaptic neurotransmitter release, and altering intracellular second messenger-mediated signaling pathways. Here, we summarize the signal pathways associated with α7-nAChR activation involving nucleotides, ions, lipids, and gas molecules. This article provides insights into α7-nAChR-mediated modulations through intracellular signaling systems and helps to understand the α7-nAChR-associated pathogenesis and therapeutics of a variety of diseases and disorders.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信