Similarities and differences between the responses induced in human phagocytes through activation of the medium chain fatty acid receptor GPR84 and the short chain fatty acid receptor FFA2R |
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Authors: | Martina Sundqvist Karin Christenson André Holdfeldt Michael Gabl Jonas Mårtensson Lena Björkman Regis Dieckmann Claes Dahlgren Huamei Forsman |
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Affiliation: | 1. Department of Rheumatology and Inflammation Research, Sahlgrenska, Academy, University of Gothenburg, Gothenburg, Sweden;2. Department of Oral Microbiology and Immunology, Institute of Odontology, Sahlgrenska Academy, University of Gothenburg, Sweden |
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Abstract: | GPR84 is a recently de-orphanized member of the G-protein coupled receptor (GPCR) family recognizing medium chain fatty acids, and has been suggested to play important roles in inflammation. Due to the lack of potent and selective GPR84 ligands, the basic knowledge related to GPR84 functions is very limited. In this study, we have characterized the GPR84 activation profile and regulation mechanism in human phagocytes, using two recently developed small molecules that specifically target GPR84 agonistically (ZQ16) and antagonistically (GLPG1205), respectively. Compared to our earlier characterization of the short chain fatty acid receptor FFA2R which is functionally expressed in neutrophils but not in monocytes, GPR84 is expressed in both cell types and in monocyte-derived macrophages. In neutrophils, the GPR84 agonist had an activation profile very similar to that of FFA2R. The GPR84-mediated superoxide release was low in naïve cells, but the response could be significantly primed by TNFα and by the actin cytoskeleton disrupting agent Latrunculin A. Similar to that of FFA2R, a desensitization mechanism bypassing the actin cytoskeleton was utilized by GPR84. All ZQ16-mediated cellular responses were sensitive to GLPG1205, confirming the GPR84-dependency. Finally, our data of in vivo transmigrated tissue neutrophils indicate that both GPR84 and FFA2R are involved in neutrophil recruitment processes in vivo.In summary, we show functional similarities but also some important differences between GPR84 and FFA2R in human phagocytes, thus providing some mechanistic insights into GPR84 regulation in blood neutrophils and cells recruited to an aseptic inflammatory site in vivo. |
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Keywords: | APC allophycocyaninin AU arbitrary units BSA bovine serum albumin C5aR complement fragment 5a receptor CI confidence interval Cmp1 Compound 1 CTAB Hexadecyltrimethylammonium bromide DMSO dimethyl sulfoxide FCS fetal calf serum FFAs free fatty acids FFARs free fatty acid receptors FITC fluorescein FPR formyl peptide receptors GPCR G-protein coupled receptor HRP horseradish peroxidase IL-8 interleukin 8 KRG Krebs-Ringer phosphate buffer M-CSF macrophage colony-stimulating factor MCFAs medium chain fatty acids MDMs monocyte-derived macrophages Mcpm Mega counts per minute PAFR platelet activating factor receptor PFA paraformaldehyde PE phycoerythrin PBMCs peripheral blood mononuclear cells PEST Penicillin-Streptomycin LA Latrunculin A PTX pertussis toxin RLU relative light units ROS reactive oxygen species SCFAs short-chain fatty acids TNFα tumour necrosis factor α G-protein coupled receptors Free fatty acids NADPH-oxidase Neutrophils Monocytes |
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