Anti-inflammatory signaling through G protein-coupled receptors

被引:0
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作者
Yun-jun Ge
Qi-wen Liao
Ye-chun Xu
Qiang Zhao
Bei-li Wu
Richard D. Ye
机构
[1] University of Macau,Institute of Chinese Medical Sciences
[2] The Chinese University of Hong Kong,School of Life and Health Sciences
[3] Chinese Academy of Sciences,CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica
[4] University of Chinese Academy of Sciences,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica
[5] Chinese Academy of Sciences,undefined
来源
Acta Pharmacologica Sinica | 2020年 / 41卷
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摘要
G protein-coupled receptors (GPCRs) play important roles in human physiology. GPCRs are involved in immunoregulation including regulation of the inflammatory response. Chemotaxis of phagocytes and lymphocytes is mediated to a great extent by the GPCRs for chemoattractants including myriads of chemokines. Accumulation and activation of phagocytes at the site of inflammation contribute to local inflammatory response. A handful of GPCRs have been found to transduce anti-inflammatory signals that promote resolution of inflammation. These GPCRs interact with selected metabolites of arachdonic acid, such as lipoxins, and of omega-3 essential fatty acids, such as resolvins and protectins. Despite mounting evidence for the in vivo functions of these anti-inflammatory and pro-resolving ligands paired with their respective GPCRs, the underlying signaling mechanisms have not been fully delineated. The present review summarizes what we have learned about these GPCRs, their structures and signaling pathways and the prospect of targeting these receptors for novel anti-inflammatory therapies.
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页码:1531 / 1538
页数:7
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