FEBS Letters · 1999 · 199 citations · 28 references
Life SciencesImmunologyMolecular BiologyCell SignalingGene ExpressionSignal TransductionCytokine BiologyCytokine RegulationCytokine SignalingInflammatory MediatorsInflammatory SignalingMacrophage BiologyInhibitor SpecificityJak-stat Signaling PathwayMacrophage Signaling PathwaysP38 Mitogen-activated Protein Kinase SignalingStat3 Signaling
Recent findings indicate that cytokine signaling can be modulated by other mediators of simultaneously activated signal transduction pathways. In this study we show that LPS and TNFalpha are potent inhibitors of IL-6-mediated STAT3 activation in human monocyte derived macrophages, rat liver macrophages and RAW 264.7 mouse macrophages but not in human hepatoma cells (HepG2) or in rat hepatocytes. Accordingly, LPS and TNFalpha were found to induce the expression of SOCS3 mRNA in each of the investigated type of macrophages but not in HepG2 cells. Using a specific inhibitor, evidence is presented that the p38 MAP kinase might be involved, especially for the inhibitory effect of TNFalpha.
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