Insights into the role of the resolvin D2-GPR18 signaling axis in cardiovascular physiology and disease.

Q1 Pharmacology, Toxicology and Pharmaceutics
Matthew Spite, Gabrielle Fredman
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引用次数: 0

Abstract

Non-resolving inflammation is an underpinning of cardiovascular diseases including atherosclerosis. The resolution of inflammation is an active and highly coordinated process that involves the generation of specialized pro-resolving mediators (SPMs), and other factors including proteins, gases, and nucleotides. SPMs comprise a superfamily of lipid mediators that includes lipoxins, resolvins, maresins and protectins. SPMs act through distinct G protein-coupled receptors (GPCRs) and have been extensively studied in animal models of cardiovascular diseases. An emerging body of literature suggests that SPMs have protective roles in atherosclerosis as demonstrated using specific SPM as well as mice deficient in their receptors. This review will highlight a relatively new pro-resolving signaling axis, namely Resolvin D2-GPR18, and how understanding detailed mechanisms and cellular specificity of this signaling axis may help inform the development of more targeted pro-resolution therapies for atherosclerosis and related cardiovascular pathologies.

解析蛋白D2-GPR18信号轴在心血管生理和疾病中的作用
不消炎是包括动脉粥样硬化在内的心血管疾病的基础。炎症的消退是一个积极和高度协调的过程,涉及产生专门的促消退介质(SPMs)和其他因素,包括蛋白质、气体和核苷酸。SPMs包含一个脂质介质超家族,包括脂质毒素、分解蛋白、蛋白和保护蛋白。SPMs通过不同的G蛋白偶联受体(gpcr)起作用,并在心血管疾病的动物模型中得到广泛研究。越来越多的文献表明,SPM在动脉粥样硬化中具有保护作用,这是通过使用特异性SPM和缺乏其受体的小鼠来证明的。这篇综述将重点介绍一个相对较新的促溶解信号轴,即Resolvin D2-GPR18,以及了解该信号轴的详细机制和细胞特异性如何有助于开发更有针对性的促溶解治疗动脉粥样硬化和相关心血管疾病。
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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来源期刊
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
自引率
0.00%
发文量
45
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