Publication | Open Access
Negative Regulation by Phosphatidylinositol 3-Kinase of Inducible Nitric Oxide Synthase Expression in Macrophages
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Citations
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References
1999
Year
Phosphatidylinositol 3-KinaseNitric OxideImmunologyCellular PhysiologyInflammationTranscriptional RegulationSignaling PathwayReactive Nitrogen SpecieAbstract TriggeringCell SignalingMolecular SignalingNegative RegulationCell BiologyProtein PhosphorylationPhagocyteCytokineSignal TransductionActivated MacrophagesCellular BiochemistryMedicineNitrosative Stress
Abstract Triggering of the macrophage cell line RAW 264.7 with LPS promotes a transient activation of phosphatidylinositol 3-kinase (PI3-kinase). Incubation of activated macrophages with wortmannin and LY294002, two inhibitors of PI3-kinase, increased the amount of inducible nitric oxide synthase (iNOS) and the synthesis of nitric oxide. Treatment with wortmannin promoted a prolonged activation of NF-κB in LPS-treated cells as well as an increase in the promoter activity of the iNOS gene as deduced from transfection experiments using a 1.7-kb fragment of the 5′ flanking region of the iNOS gene. Cotransfection of cells with a catalytically active p110 subunit of PI3-kinase impaired the responsiveness of the iNOS promoter to LPS stimulation, whereas transfection with a kinase-deficient mutant of p110 maintained the up-regulation in response to wortmannin. These results indicate that PI3-kinase plays a negative role in the process of macrophage activation and suggest that this enzyme might participate in the mechanism of action of antiinflammatory cytokines.
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