Interleukin-12 gene-expression of macrophages is regulated by nitric oxide

被引:49
作者
Rothe, H [1 ]
Hartmann, B [1 ]
Geerlings, P [1 ]
Kolb, H [1 ]
机构
[1] UNIV DUSSELDORF,DIABET RES INST,D-40225 DUSSELDORF,GERMANY
关键词
D O I
10.1006/bbrc.1996.1000
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
Interleukin-12 is a heterodimeric cytokine, mainly produced by macrophages. In our present study we demonstrate that interleukin-12 expression is regulated by nitric oxide. Incubation of the macrophage cell line IC 21 with interferon-gamma gave rise to both interleukin-12 p40 mRNA and nitric oxide production. The concurrent addition of the nitric oxide synthase inhibitor N-G-monomethyl-L-arginine inhibited nitrite production and in parallel completely suppressed interleukin-12 p40 mRNA formation. This indicated that endogenous nitric oxide synthase activity was required for IL-12 p40 gene expression. Exposure of the cells towards the nitric oxide generating compounds nitroprusside or S-nitroso-N-acetyl-penicillamine induced interleukin-12 p40 mRNA. Maximal mRNA levels were induced with nitric oxide donors at 1 mu M concentration. We conclude that nitric oxide may exert an autoregulatory and paracrine control of interleukin-12 gene expression. (C) 1996 Academic Press, Inc.
引用
收藏
页码:159 / 163
页数:5
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