LAUSR

HighlightsIL‐33 stimulates expression of the GPR84 fatty acid receptor gene in human adipocytes.IL‐33 also induces strong expression of the IL1B, CCL2, IL6, CXCL2 and CSF3 genes.ADIPOQ (adiponectin) expression is not altered by IL‐33.Secretion of G‐CSF protein (encoded by CSF3) from adipocytes is stimulated by IL‐33. &NA; Expression of GPCR fatty acid sensor/receptor genes in adipocytes is modulated by inflammatory mediators, particularly IL‐1&bgr;. In this study we examined whether the IL‐1 gene superfamily member, IL‐33, also regulates expression of the fatty acid receptor genes in adipocytes. Human fat cells, differentiated from preadipocytes, were incubated with IL‐33 at three different dose levels for 3 or 24 h and mRNA measured by qPCR. Treatment with IL‐33 induced a dose‐dependent increase in GPR84 mRNA at 3 h, the level with the highest dose being 13.7‐fold greater than in controls. Stimulation of GPR84 expression was transitory; the mRNA level was not elevated at 24 h. In contrast to GPR84, IL‐33 had no effect on GPR120 expression. IL‐33 markedly stimulated expression of the IL1B, CCL2, IL6, CXCL2 and CSF3 genes, but there was no effect on ADIPOQ expression. The largest effect was on CSF3, the mRNA level of which increased 183‐fold over controls at 3 h with the highest dose of IL‐33; there was a parallel increase in the secretion of G‐CSF protein into the medium. It is concluded that in human adipocytes IL‐33, which is synthesised in adipose tissue, has a strong stimulatory effect on the expression of cytokine and chemokine genes, particularly CSF3, and on the expression of GPR84, a pro‐inflammatory fatty acid receptor.