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促炎 G 蛋白偶联受体 GPR84 的调节。

Regulation of the pro-inflammatory G protein-coupled receptor GPR84.

机构信息

Centre for Translational Pharmacology, School of Molecular Biosciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.

出版信息

Br J Pharmacol. 2024 May;181(10):1500-1508. doi: 10.1111/bph.16098. Epub 2023 May 11.

Abstract

GPR84 is an understudied rhodopsin-like class A G protein-coupled receptor, which is arousing particular interest from a therapeutic perspective. Not least this reflects that gpr84 expression is significantly up-regulated following acute inflammatory stimuli and in inflammatory diseases, and that receptor activation plays a role in regulating pro-inflammatory responses and migration of cells of the innate immune system such as neutrophils, monocytes, macrophages and microglia. Although most physiological responses of GPR84 reflect receptor coupling to G-proteins, several studies indicate that agonist-activated GPR84 can recruit arrestin adaptor proteins and this regulates receptor internalisation and desensitisation. To date, little is known on the patterns of either basal or ligand regulated GPR84 phosphorylation and how these might control these processes. Here, we consider what is known about the regulation of GPR84 signalling with a focus on how G protein receptor kinase-mediated phosphorylation regulates arrestin protein recruitment and receptor function. LINKED ARTICLES: This article is part of a themed issue GPR84 Pharmacology. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.10/issuetoc.

摘要

GPR84 是一种研究较少的视紫红质样 A 类 G 蛋白偶联受体,从治疗的角度来看,它引起了人们的特别关注。这在一定程度上反映了 gpr84 的表达在急性炎症刺激和炎症性疾病后显著上调,并且受体激活在调节先天免疫系统细胞(如中性粒细胞、单核细胞、巨噬细胞和小胶质细胞)的促炎反应和迁移中发挥作用。尽管 GPR84 的大多数生理反应反映了受体与 G 蛋白的偶联,但有几项研究表明,激动剂激活的 GPR84 可以募集阻滞蛋白衔接蛋白,这调节受体内化和脱敏。迄今为止,人们对 GPR84 的基础或配体调节磷酸化模式知之甚少,也不知道这些模式如何控制这些过程。在这里,我们考虑了 GPR84 信号转导的调节,重点是 G 蛋白受体激酶介导的磷酸化如何调节阻滞蛋白的招募和受体功能。相关文章:本文是 GPR84 药理学专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.10/issuetoc.

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