School of Pharmacy, Shanghai Jiao Tong University, China.
Acta Pharmacol Sin. 2012 Mar;33(3):342-50. doi: 10.1038/aps.2011.200. Epub 2012 Feb 27.
G protein-coupled receptors (GPCRs) play important roles in inflammation. Inflammatory cells such as polymorphonuclear leukocytes (PMN), monocytes and macrophages express a large number of GPCRs for classic chemoattractants and chemokines. These receptors are critical to the migration of phagocytes and their accumulation at sites of inflammation, where these cells can exacerbate inflammation but also contribute to its resolution. Besides chemoattractant GPCRs, protease activated receptors (PARs) such as PAR1 are involved in the regulation of vascular endothelial permeability. Prostaglandin receptors play different roles in inflammatory cell activation, and can mediate both proinflammatory and anti-inflammatory functions. Many GPCRs present in inflammatory cells also mediate transcription factor activation, resulting in the synthesis and secretion of inflammatory factors and, in some cases, molecules that suppress inflammation. An understanding of the signaling paradigms of GPCRs in inflammatory cells is likely to facilitate translational research and development of improved anti-inflammatory therapies.
G 蛋白偶联受体(GPCRs)在炎症中发挥重要作用。炎性细胞,如多形核白细胞(PMN)、单核细胞和巨噬细胞,表达大量的 GPCRs,用于经典趋化因子和趋化素。这些受体对于吞噬细胞的迁移及其在炎症部位的积聚至关重要,在炎症部位,这些细胞可以加剧炎症,但也有助于其解决。除了趋化因子 GPCRs 外,蛋白酶激活受体(PARs)如 PAR1 也参与血管内皮通透性的调节。前列腺素受体在炎症细胞的激活中发挥不同的作用,并能介导促炎和抗炎功能。炎性细胞中存在的许多 GPCRs 也介导转录因子的激活,导致炎症因子的合成和分泌,在某些情况下,还会产生抑制炎症的分子。了解 GPCRs 在炎症细胞中的信号传递模式可能有助于转化研究和开发改善的抗炎治疗方法。