Agonists for G-protein-coupled receptor 84 (GPR84) alter cellular morphology and motility but do not induce pro-inflammatory responses in microglia

J Neuroinflammation. 2017 Oct 3;14(1):198. doi: 10.1186/s12974-017-0970-y.

Abstract

Background: Several G-protein-coupled receptors (GPCRs) have been shown to be important signaling mediators between neurons and glia. In our previous screening for identification of nerve injury-associated GPCRs, G-protein-coupled receptor 84 (GPR84) mRNA showed the highest up-regulation by microglia after nerve injury. GPR84 is a pro-inflammatory receptor of macrophages in a neuropathic pain mouse model, yet its function in resident microglia in the central nervous system is poorly understood.

Methods: We used endogenous, natural, and surrogate agonists for GPR84 (capric acid, embelin, and 6-OAU, respectively) and examined their effect on mouse primary cultured microglia in vitro.

Results: 6-n-Octylaminouracil (6-OAU), embelin, and capric acid rapidly induced membrane ruffling and motility in cultured microglia obtained from C57BL/6 mice, although these agonists failed to promote microglial pro-inflammatory cytokine expression. Concomitantly, 6-OAU suppressed forskolin-induced increase of cAMP in cultured microglia. Pertussis toxin, an inhibitor of Gi-coupled signaling, completely suppressed 6-OAU-induced microglial membrane ruffling and motility. In contrast, no 6-OAU-induced microglial membrane ruffling and motility was observed in microglia from DBA/2 mice, a mouse strain that does not express functional GPR84 protein due to endogenous nonsense mutation of the GPR84 gene.

Conclusions: GPR84 mediated signaling causes microglial motility and membrane ruffling but does not promote pro-inflammatory responses. As GPR84 is a known receptor for medium-chain fatty acids, those released from damaged brain cells may be involved in the enhancement of microglial motility through GPR84 after neuronal injury.

Keywords: Fatty acid; G-protein-coupled receptor 84; Microglia morphology; Microglia motility; Pro-inflammatory response.

MeSH terms

  • Animals
  • Animals, Newborn
  • Benzoquinones / pharmacology
  • Cell Movement / drug effects*
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Cyclic AMP / metabolism
  • Cytokines / genetics
  • Cytokines / metabolism
  • Decanoic Acids / pharmacology
  • Gene Deletion
  • Macrophages / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Microglia / drug effects*
  • Microglia / immunology
  • Nitric Oxide Synthase Type II / metabolism
  • Pertussis Toxin / pharmacology
  • Receptors, G-Protein-Coupled / agonists*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction / drug effects
  • Uracil / pharmacology

Substances

  • Benzoquinones
  • Cytokines
  • Decanoic Acids
  • Gpr84 protein, mouse
  • Receptors, G-Protein-Coupled
  • decanoic acid
  • Uracil
  • Cyclic AMP
  • Nitric Oxide Synthase Type II
  • Pertussis Toxin
  • embelin