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降钙素基因相关肽受体对信号转导的调节。

Regulation of signal transduction by calcitonin gene-related peptide receptors.

机构信息

School of Biological Sciences, and Centre for Brain Research, University of Auckland, Auckland, New Zealand.

出版信息

Trends Pharmacol Sci. 2010 Oct;31(10):476-83. doi: 10.1016/j.tips.2010.06.006. Epub 2010 Jul 13.

Abstract

Calcitonin gene-related peptide (CGRP) plays a pivotal role in migraine, activating its cognate receptor to initiate intracellular signalling. This atypical receptor comprises a distinct assembly, made up of a G protein-coupled receptor (GPCR), a single transmembrane protein, and an additional protein that is required for Gα(s) coupling. By altering the expression of individual receptor components, it might be possible to adjust cellular sensitivity to CGRP. In recognition of the increasing clinical significance of CGRP receptors, it is timely to review the signalling pathways that might be controlled by this receptor, how the activity of the receptor itself is regulated, and our current understanding of the molecular mechanisms involved in these processes. Like many GPCRs, the CGRP receptor appears to be promiscuous, potentially coupling to several G proteins and intracellular pathways. Their precise composition is likely to be cell type-dependent, and much work is needed to ascertain their physiological significance.

摘要

降钙素基因相关肽 (CGRP) 在偏头痛中发挥着关键作用,它能激活其同源受体以启动细胞内信号转导。这种非典型受体由一个独特的组件构成,包括一个 G 蛋白偶联受体 (GPCR)、一个单一的跨膜蛋白和一个额外的蛋白质,该蛋白质是 Gα(s) 偶联所必需的。通过改变单个受体成分的表达,有可能调节细胞对 CGRP 的敏感性。鉴于 CGRP 受体的临床重要性日益增加,及时回顾该受体可能控制的信号通路、受体本身的活性如何受到调节以及我们对这些过程中涉及的分子机制的理解是很有必要的。与许多 GPCR 一样,CGRP 受体似乎很混杂,可能与几种 G 蛋白和细胞内途径偶联。它们的确切组成可能依赖于细胞类型,需要做大量的工作来确定它们的生理意义。

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