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Differential regulation of inducible nitric oxide synthase and cyclooxygenase-2 expression by superoxide dismutase in lipopolysaccharide stimulated RAW 264.7 cells
Article de En | WPRIM | ID: wpr-10783
Bibliothèque responsable: WPRO
ABSTRACT
Inducible nitric oxide synthase (iNOS) and cyclooxygenase 2 (COX-2) have been known to be involved in various pathophysiological processes such as inflammation. This study was performed to determine the regulatory function of superoxide dismutase (SOD) on the LPS-induced expression of iNOS, and COX-2 in RAW 264.7 cells. When a cell-permeable SOD, Tat-SOD, was added to the culture medium of RAW 264.7 cells, it rapidly entered the cells in a dose-dependent manner. Treatment of RAW 264.7 cells with Tat-SOD led to decrease in LPS-induced ROS generation. Pretreatment with Tat-SOD significantly inhibited LPS-induced expression of iNOS and NO production but had no effect on the expression of COX-2 and PGE2 production in RAW 264.7 cells. Tat-SOD inhibited LPS-induced NF-kappaB DNA binding activity, IkappaBalpha degradation and activation of MAP kinases. These data suggest that SOD differentially regulate expression of iNOS and COX-2 in LPS-stimulated RAW 264.7 cells.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Superoxide dismutase / Lignée cellulaire / Régulation de l'expression des gènes / Lipopolysaccharides / Cytokines / Facteur de transcription NF-kappa B / Espèces réactives de l'oxygène / Mitogen-Activated Protein Kinase Kinases / Cyclooxygenase 2 / Nitric oxide synthase type II Limites du sujet: Animals langue: En Texte intégral: Experimental & Molecular Medicine Année: 2009 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Superoxide dismutase / Lignée cellulaire / Régulation de l'expression des gènes / Lipopolysaccharides / Cytokines / Facteur de transcription NF-kappa B / Espèces réactives de l'oxygène / Mitogen-Activated Protein Kinase Kinases / Cyclooxygenase 2 / Nitric oxide synthase type II Limites du sujet: Animals langue: En Texte intégral: Experimental & Molecular Medicine Année: 2009 Type: Article