GPR120的功能特性及其抗动脉粥样硬化机制研究

The functional characteristics of GPR120 and its mechanism in preventing atherosclerosis

  • 摘要: 游离脂肪酸是机体调节能量代谢的重要物质,主要通过与细胞膜上的G蛋白偶联受体(GPRs)结合并发挥功能。G蛋白偶联受体120(GPR120)是哺乳动物体内中、长链游离脂肪酸的受体。研究显示,内皮细胞、血管平滑肌细胞和单核/巨噬细胞上GPR120的激活可降低单核细胞黏附、促进泡沫细胞内胆固醇流出、调控巨噬细胞的迁移和分化,发挥抗炎、抗氧化等功能,具有抵抗动脉粥样硬化的潜在作用。文章综述了GPR120的分子结构、组织分布、配体类型、信号转导途径及其在抗动脉粥样硬化疾病中的研究进展,旨在揭示GPR120抗动脉粥样硬化的分子机制及其作为治疗靶点的潜在价值。

     

    Abstract: Free fatty acids are important substances for regulating energy metabolism in the body and mainly exert their functions by binding to G protein-coupled receptors(GPRs)on the cell membrane. GPR120 is the receptor for medium and long-chain free fatty acids in mammals. Studies have found that the activation of GPR120 on endothelial cells,vascular smooth muscle cells,and monocytes/macrophages can reduce monocyte adhesion,promote cholesterol efflux from foam cells,regulate the migration and differentiation of macrophages,and exert anti-inflammatory and antioxidant functions,potentially resisting atherosclerosis. This article reviews the molecular structure,tissue distribution,ligand types,signal transduction pathways of GPR120,and its research progress in anti-atherosclerotic diseases,aiming to reveal the molecular mechanism of GPR120 in resisting atherosclerosis and its potential value as a therapeutic target.

     

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