Role of the cyclic AMP-protein kinase A pathway in lipopolysaccharide- induced nitric oxide synthase expression in RAW 264.7 macrophages. Involvement of cyclooxygenase-2
Journal
Journal of Biological Chemistry
Journal Volume
274
Journal Issue
44
Pages
31559-31564
Date Issued
1999
Author(s)
Abstract
The signaling pathway for lipopolysaccharide (LPS)-induced nitric oxide (NO) release in RAW 264.7 macrophages involves the protein kinase C and p38 activation pathways (Chen, C. C., Wang, J. K., and Lin, S. B. (1998) J. Immunol. 161, 6206-6214; Chen, C. C., and Wang, J. K. (1999) Mol. Pharmacol. 55, 481-488). In this study, the role of the cAMP-dependent protein kinase A (PKA) pathway was investigated. The PKA inhibitors, KT-5720 and H8, reduced LPS-induced NO release and inducible nitric oxide synthase (iNOS) expression. The direct PKA activator, Bt2cAMP, caused concentration-dependent NO release and iNOS expression, as confirmed by immunofluorescence studies. The intracellular cAMP concentration did not increase until after 6 h of LPS treatment. Two cAMP-elevating agents, forskolin and cholera toxin, potentiated the LPS-induced NO release and iNOS expression. Stimulation of cells with LPS or Bt2cAMP for periods of 10 rain to 24 h caused nuclear factor-κB (NF-κB) activation in the nuclei, as shown by detection of NF- κB-specific DNA-protein binding. The PKA inhibitor, H8, inhibited the NF-κB activation induced by 6- or 12-h treatment with LPS but not that induced after 1, 3, or 24 h. The cyclooxygenase-2 (COX-2) inhibitors, NS-398 and indomethacin, attenuated LPS-induced NO release, iNOS expression, and NF-κB DNA-protein complex formation. LPS induced COX-2 expression in a time- dependent manner, and prostaglandin E2 production was induced in parallel. These results suggest that 6 h of treatment with LPS increases intracellular cAMP levels via COX-2 induction and prostaglandin E2 production, resulting in PKA activation, NF-κB activation, iNOS expression, and NO production.
Other Subjects
bacterium lipopolysaccharide; bucladesine; cell DNA; cholera toxin; cyclic AMP; cyclic AMP dependent protein kinase; cyclooxygenase 2; forskolin; immunoglobulin enhancer binding protein; indometacin; kt 5720; n (2 cyclohexyloxy 4 nitrophenyl)methanesulfonamide; n (2 methylaminoethyl) 5 isoquinolinesulfonamide; nitric oxide; nitric oxide synthase; nitrite; prostaglandin e2; animal cell; article; binding kinetics; cell level; cell stimulation; cellular distribution; concentration response; controlled study; dose time effect relation; enzyme activation; enzyme assay; enzyme localization; incubation time; macrophage; molecular dynamics; mouse; nonhuman; priority journal; prostaglandin release; protein DNA binding; protein expression; protein induction; Animals; Bucladesine; Cell Compartmentation; Cell Line; Cholera Toxin; Cyclic AMP-Dependent Protein Kinases; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Cytoplasm; Forskolin; Isoenzymes; Isoquinolines; Lipopolysaccharides; Macrophages; Mice; Models, Biological; NF-kappa B; Nitric Oxide Synthase; Nitric Oxide Synthase Type II; Nitrites; Prostaglandin-Endoperoxide Synthases; Signal Transduction
Type
journal article