STAT1 is required for iNOS activation, but not IL-6 production in murine fibroblasts

被引:39
|
作者
Samardzic, T
Jankovic, V
Stosic-Grujicic, S
Trajkovic, V
机构
[1] Inst Biol Res Dr Sinisa Stankovic, YU-11000 Belgrade, Yugoslavia
[2] Univ Belgrade, Sch Med, Inst Microbiol & Immunol, Belgrade, Yugoslavia
关键词
nitric oxide; IL-6; STAT1; fibroblast;
D O I
10.1006/cyto.2000.0785
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The role of transcription factor STAT1 in production of pro-inflammatory mediators nitric oxide (NO) and IL-6 was examined in murine embryonic fibroblasts. While cells from wild-type animals released large amounts of NO after stimulation with IFN-gamma in combination with LPS, TNF-alpha or IL-1, their STAT1-deficient counterparts failed to synthesise detectable levels of this free radical gas. Inability of STAT1(-/-) fibroblasts to produce NO was accompanied by complete absence of mRNA for iNOS and its transcription factor IRF-1, both readily upregulated in wild-type cells. However, treatment with cytokines (IFN-gamma, TNF-alpha, IL-1, IL-17) significantly increased IL-6 generation in STAT1-deficient fibroblasts. These results indicate that STAT1 activation and subsequent IRF-1 transcription are required for induction of iNOS, but not IL-6 in murine fibroblasts. (C) 2001 Academic Press.
引用
收藏
页码:179 / 182
页数:4
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