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5-Aza-2′-deoxycytidine stimulates inducible nitric oxide synthase induction in C6 astrocytoma cells
被引:4
|作者:
Cvetkovic, I
Popadic, D
Vuckovic, O
Harhaji, L
Miljkovic, D
Trajkovic, V
机构:
[1] Inst Biol Res, Immunol Lab, YU-11000 Belgrade, Serbia
[2] Univ Belgrade, Sch Med, Inst Microbiol & Immunol, Belgrade, Serbia
关键词:
5-Aza-2 '-deoxycytidine;
astrocyte;
nitric oxide;
iNOS;
D O I:
10.1016/j.brainres.2003.11.014
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The influence of a nucleoside analog 5-aza-2'-deoxycytidine (5-AzadC) on inducible nitric oxide synthase (iNOS)-dependent nitric oxide (NO) production in various rat cell types was investigated. In C6 astrocytoma cell line and primary astrocytes, 5-AzadC enhanced proinflammatory cytokine (IFN-gamma, TNT-alpha, IL-1)-triggered NO synthesis in a time- and dose-dependent manner. In contrast, 5-AzadC did not potentiate NO production in IFN-gamma-stimulated macrophages, fibroblasts, or endothelial cells. Blockade of transcription or translation in C6 cells abolished the observed effect, suggesting the NOS gene expression, rather than its catalytic activity, as a target for the drug action. Accordingly, 5-AzadC upregulated IFN-gamma-induced expression of iNOS mRNA in C6 astrocytes. The effect of 5-AzadC on astrocyte NO release was blocked by the inhibitor of p44/42 mitogen activated protein kinase-dependent signaling. Finally, the observed stimulatory effect of 5-AzadC on iNOS expression was apparently independent of DNA demethylation, as DNA digestion with methylation-sensitive restriction enzyme Hpall showed that 5-AzadC failed to demethylate cellular DNA in conditions used for iNOS induction. (C) 2003 Elsevier B.V. All rights reserved.
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页码:83 / 90
页数:8
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