Immunology · 1999 · 240 citations · 31 references
Life SciencesCell BiologyImmunologyCell SignalingInflammationSignal TransductionAnti-inflammatory PharmacologyCytokine BiologyInflammatory SignalingMacrophage BiologyMacrophage Inflammatory ResponsesMacrophage Signaling PathwaysMacrophage-mediated InflammationMitogen-activated Protein Kinase KinaseMitogen-activated Protein Kinase ModulationNitric Oxide Signaling ModulationP38 Mitogen-activated Protein Kinase SignalingProstaglandin Production
Both the nitrite and prostaglandin E2 (PGE2) release caused by lipopolysaccharide (LPS) in J774 macrophages are inhibited by SB 203580, a specific p38 mitogen-activated protein kinase (MAPK) inhibitor, in a concentration-dependent manner. The 50% inhibitory concentration (IC50) for nitrite and PGE2 responses was 1 microm and 0.5 microm, respectively. Inhibition was marked following simultaneous treatment with SB 203580 and LPS, and was much reduced when SB 203580 was added 6 hr after LPS treatment. In parallel, LPS induction of inducible NO synthase (iNOS) and cyclo-oxygenase-2 (COX-2) proteins and their steady-state levels of mRNA were reduced by SB 203580. LPS activation of nuclear factor-kappa B (NF-kappaB), activator protein-1 (AP-1) and p38 MAPK was also inhibited by SB 203580. These results suggest a crucial role of p38 MAPK in regulation of the transcriptional level of endotoxin LPS-induced iNOS and COX-2 protein expression.
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