Medium-chain Fatty Acid-sensing Receptor, GPR84, Is a Proinflammatory Receptor
G protein-coupled receptor 84 (GPR84) is a putative receptor for medium-chain fatty acids (MCFAs), whose pathophysiological roles have not yet been clarified. Here, we show that GPR84 was activated by MCFAs with the hydroxyl group at the 2- or 3-position more effectively than nonhydroxylated MCFAs....
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Veröffentlicht in: | The Journal of biological chemistry 2013-04, Vol.288 (15), p.10684-10691 |
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Sprache: | eng |
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Zusammenfassung: | G protein-coupled receptor 84 (GPR84) is a putative receptor for medium-chain fatty acids (MCFAs), whose pathophysiological roles have not yet been clarified. Here, we show that GPR84 was activated by MCFAs with the hydroxyl group at the 2- or 3-position more effectively than nonhydroxylated MCFAs. We also identified a surrogate agonist, 6-n-octylaminouracil (6-OAU), for GPR84. These potential ligands and the surrogate agonist, 6-OAU, stimulated [35S]GTP binding and accumulated phosphoinositides in a GPR84-dependent manner. The surrogate agonist, 6-OAU, internalized GPR84-EGFP from the cell surface. Both the potential ligands and 6-OAU elicited chemotaxis of human polymorphonuclear leukocytes (PMNs) and macrophages and amplified LPS-stimulated production of the proinflammatory cytokine IL-8 from PMNs and TNFα from macrophages. Furthermore, the intravenous injection of 6-OAU raised the blood CXCL1 level in rats, and the inoculation of 6-OAU into the rat air pouch accumulated PMNs and macrophages in the site. Our results indicate a proinflammatory role of GPR84, suggesting that the receptor may be a novel target to treat chronic low grade inflammation associated-disease.
Background: The biological function of a former orphan receptor, GPR84, has not been clarified yet.
Results: GPR84 activation results in chemotaxis and cytokine production by the stimulation of potential ligands and the surrogate agonist.
Conclusion: GPR84 works as a proinflammatory receptor in myeloid cells.
Significance: This study provides new insights into the function of GPR84. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M112.420042 |