25-hydroxycholesterol-3-sulfate attenuates inflammatory response via PPAR?? signaling in human THP-1 macrophages

摘要

The nuclear receptor peroxisome proliferator-activated receptors (PPARs) are important in regulating lipid metabolism and inflammatory responses in macrophages. Activation of PPAR7 represses key inflammatory response gene expressions. Recently, we identified a new cholesterol metabolite, 25-hydroxycholesterol-3-sulfate (25HC3S), as a potent regulatory molecule of lipid metabolism. In this paper, we report the effect of 25HC3S and its precursor 25-hydroxycholesterol (25HC) on PPAR7 activity and on inflammatory responses. Addition of 25HC3S to human macrophages markedly increased nuclear PPAR?? and cytosol IkB and decreased nuclear NF-kB protein levels. PPAR?? response element reporter gene assays showed that 25HC3S significantly increased lu-ciferase activities. PPAR?? competitor assay showed that the Ki for 25HC3S was ~1 (??M, similar to those of other known natural ligands. NF-KB-dependent promoter reporter gene assays showed that 25HC3S suppressed TNF??-induced luciferase activities only when cotransfected with pcDNAI-PPAR7 plasmid. In addition, 25HC3S decreased LPS-induced expression and release of IL-1??. In the PPAR??-specific siRNA transfected macrophages or in the presence of PPAR??-specific antagonist, 25HC3S failed to increase IkB and to suppress TNF?? and IL-1?? expression. In contrast to 25HC3S, its precursor 25HC, a known liver X receptor ligand, decreased nuclear PPAR?? and cytosol IkB and increased nuclear NF-kB protein levels. We conclude that 25HC3S acts in macrophages as a PPAR?? ligand and suppresses inflammatory responses via the PPAR??/IKB/NF-KB signaling pathway. ? 2012 by the American Physiological Society.