Therapeutic validation of an orphan G protein-coupled receptor: The case of GPR84

被引:31
|
作者
Marsango, Sara [1 ]
Barki, Natasja [1 ]
Jenkins, Laura [1 ]
Tobin, Andrew B. [1 ]
Milligan, Graeme [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Inst Mol Cell & Syst Biol, Ctr Translat Pharmacol, Glasgow G12 8QQ, Lanark, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
allosteric ligand; GPCR; GPR84; inflammation; orphan receptor; orthosteric ligand; CONCISE GUIDE; GENE-EXPRESSION; GPCR STRUCTURES; MOUSE MODEL; LIGANDS; IDENTIFICATION; DISCOVERY; MICROGLIA; AGONIST; EX33;
D O I
10.1111/bph.15248
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the importance of members of the GPCR superfamily as targets of a broad range of effective medicines many GPCRs remain poorly characterised. GPR84 is an example. Expression of GPR84 is strongly up regulated in immune cells in a range of pro-inflammatory settings and clinical trials to treat idiopathic pulmonary fibrosis are currently ongoing using ligands with differing levels of selectivity and affinity as GPR84 antagonists. Although blockade of GPR84 may potentially prove effective also in diseases associated with inflammation of the lower gut there is emerging interest in defining if agonists of GPR84 might find utility in conditions in which regulation of metabolism or energy sensing is compromised. Here, we consider the physiological and pathological expression profile of GPR84 and, in the absence of direct structural information, recent developments and use of GPR84 pharmacological tool compounds to study its broader role and biology.
引用
收藏
页码:3529 / 3541
页数:13
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