The role of G protein-coupled receptor 4 in inflammatory diseases and its potential clinical significance.

Qilimuge Bai, Gegentuya Bao, Yali Yan, Saqirina Hereid, Xiaohong Bai, Liang Bao
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引用次数: 0

Abstract

G protein-coupled receptor 4 (GPR4) is a dual ligand receptor that can be activated by both protons and lysophosphatidylcholine (LPC), which is a bioactive phospholipid. It plays a pivotal role in numerous physiological and pathological processes and is regulated by these two ligands through distinct mechanisms. Recently, there has been growing interest in the role of GPR4 in diseases characterized by an acidic microenvironment. This review aims to explore the specific signaling pathways through which protons and LPC regulate GPR4 in the inflammatory microenvironment and to clarify the distinct roles of these ligands in various diseases, including inflammation, atherosclerosis, and cancer. Additionally, the potential benefits and challenges of targeting GPR4 as a therapeutic strategy for these diseases are analyzed.

G蛋白偶联受体4在炎症性疾病中的作用及其潜在的临床意义
G蛋白偶联受体4 (GPR4)是一种双配体受体,可被质子和溶血磷脂(LPC)激活。它在许多生理和病理过程中起着关键作用,并通过不同的机制受到这两种配体的调节。最近,人们对GPR4在以酸性微环境为特征的疾病中的作用越来越感兴趣。本文旨在探讨质子和LPC在炎症微环境中调控GPR4的具体信号通路,并阐明这些配体在炎症、动脉粥样硬化和癌症等多种疾病中的独特作用。此外,本文还分析了靶向GPR4作为这些疾病的治疗策略的潜在益处和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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