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
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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.
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