Literature DB >> 9138702

Differential regulation by protein kinase C isoforms of nitric oxide synthase induction in RAW 264.7 macrophages and rat aortic smooth muscle cells.

A Paul1, K Doherty, R Plevin.   

Abstract

1. In RAW 264.7 murine macrophages and rat aortic smooth muscle (RASM) cells lipopolysaccharide (LPS) alone or in combination with interferon gamma (IFN gamma) or forskolin, respectively, stimulated the expression of the 130 kDa inducible isoform of nitric oxide synthase (iNOS) in both a time- and concentration-dependent manner. 2. Incubation with the direct activator of protein kinase C (PKC), phorbol 12-myristate 13-acetate (PMA) alone, did not result in detectable iNOS expression in either cell type. 3. Chronic PMA pretreatment resulted in significant down-regulation of alpha, beta and epsilon isforms of PKC in RAW 264.7 macrophages and corresponded to a 20-30% reduction in LPS-induced iNOS expression. In contrast, IFN gamma alone or in combination with LPS stimulated an approximate 20% and 50% potentiation, respectively. 4. Pre-incubation with PKC inhibitors (calphostin C and H-7) showed similar effects upon stimulated induction of iNOS. 5. In RASM cells chronic PMA pretreatment resulted in down-regulation of alpha and epsilon PKC isoforms and corresponded to potentiation of iNOS expression in response to LPS alone or in combination with forskolin. 6. Co-incubation of RASM cells in the presence of PMA, angiotensin II (AII) or foetal calf serum (FCS) resulted in the inhibition of iNOS expression in response to LPS alone or in combination with forskolin. 7. Differential sensitivity to PKC inhibitors (calphostin C and H-7) was observed in RASM cells and exhibited both negative and positive modulation of stimulated induction. 8. In addition the PKC inhibitor compound Ro-31-8220 abolished stimulated induction in both cell types in response to all treatments. 9. These results suggest that PKC activation is required for induction of the 130 kDa isoform of NOS in both RAW 264.7 macrophages and RASM cells. However, individual PKC isoforms regulate iNOS expression in both a positive and negative manner.

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Year:  1997        PMID: 9138702      PMCID: PMC1564539          DOI: 10.1038/sj.bjp.0700976

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  12 in total

1.  Inhibition of classical PKC isoenzymes downregulates STAT1 activation and iNOS expression in LPS-treated murine J774 macrophages.

Authors:  Tiina Salonen; Outi Sareila; Ulla Jalonen; Hannu Kankaanranta; Raimo Tuominen; Eeva Moilanen
Journal:  Br J Pharmacol       Date:  2006-04       Impact factor: 8.739

2.  Distribution of protein kinase C isoforms after infection of macrophages with Leishmania major.

Authors:  S Pingel; Z E Wang; R M Locksley
Journal:  Infect Immun       Date:  1998-04       Impact factor: 3.441

3.  Reduction of no synthase expression and tumor necrosis factor alpha production in macrophages by amphotericin B lipid carriers.

Authors:  M Larabi; P Legrand; M Appel; S Gil; M Lepoivre; J Devissaguet; F Puisieux; G Barratt
Journal:  Antimicrob Agents Chemother       Date:  2001-02       Impact factor: 5.191

4.  Selective inhibition of inhibitory kappa B kinase-beta abrogates induction of nitric oxide synthase in lipopolysaccharide-stimulated rat aortic smooth muscle cells.

Authors:  Almudena Bermejo Gomez; Christopher MacKenzie; Andrew Paul; Robin Plevin
Journal:  Br J Pharmacol       Date:  2005-09       Impact factor: 8.739

5.  Role of iNOS in the vasodilator responses induced by L-arginine in the middle cerebral artery from normotensive and hypertensive rats.

Authors:  A M Briones; M J Alonso; J Marín; M Salaices
Journal:  Br J Pharmacol       Date:  1999-01       Impact factor: 8.739

6.  Induction of nitric oxide synthesis by probiotic Lactobacillus rhamnosus GG in J774 macrophages and human T84 intestinal epithelial cells.

Authors:  R Korhonen; R Korpela; M Saxelin; M Mäki; H Kankaanranta; E Moilanen
Journal:  Inflammation       Date:  2001-08       Impact factor: 4.092

7.  Post-ischemic activation of protein kinase C ε protects the hippocampus from cerebral ischemic injury via alterations in cerebral blood flow.

Authors:  D Della-Morte; A P Raval; K R Dave; H W Lin; M A Perez-Pinzon
Journal:  Neurosci Lett       Date:  2010-10-14       Impact factor: 3.046

8.  Signalling mechanisms involved in the induction of inducible nitric oxide synthase by Lactobacillus rhamnosus GG, endotoxin, and lipoteichoic acid.

Authors:  Riku Korhonen; Riitta Korpela; Eeva Moilanen
Journal:  Inflammation       Date:  2002-10       Impact factor: 4.092

9.  Isoflurane preconditioning reduces mouse microglial activation and injury induced by lipopolysaccharide and interferon-gamma.

Authors:  X Xu; J A Kim; Z Zuo
Journal:  Neuroscience       Date:  2008-04-16       Impact factor: 3.590

10.  Delayed treatment with isoflurane attenuates lipopolysaccharide and interferon gamma-induced activation and injury of mouse microglial cells.

Authors:  Jie-Ae Kim; Liaoliao Li; Zhiyi Zuo
Journal:  Anesthesiology       Date:  2009-09       Impact factor: 7.892

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