Effects of nitric oxide on chemotaxis and endotoxin-induced interleukin-8 production in human neutrophils

被引:41
|
作者
Corriveau, CC
Madara, PJ
Van Dervort, AL
Tropea, MM
Wesley, RA
Danner, RL
机构
[1] NIH, Dept Crit Care Med, Warren Grant Magnuson Clin Ctr, Bethesda, MD 20892 USA
[2] Childrens Natl Med Ctr, Washington, DC 20010 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 1998年 / 177卷 / 01期
基金
美国国家卫生研究院;
关键词
D O I
10.1086/513829
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The effects of nitric oxide (NO) on human neutrophil chemotactic responses and release of interleukin (IL)-8 was studied. Neutrophils exposed to chemoattractants (IL-8, FMLP, leukotriene B-4, and C5a) failed to show increases in intracellular guanosine 3',5'-cyclic monophosphate (cGMP), an indicator of NO production, Although NO increased cGMP in neutrophils, neither of two NO donors (sodium nitroprusside and 3-morpholino-sydonimine) nor a NO synthase inhibitor (N-omega-nitro-L-arginine) altered FMLP-or IL-8-elicited neutrophil chemotaxis (P > .25 for all). However, lipopolysaccharide-induced IL-8 production was increased in a dose-dependent manner by a combination of sodium nitroprusside and N-acetylcysteine (P = .03) or by S-nitrosoglutathione (P = .004), NO-augmented IL-8 release was not reproduced by treating neutrophils with dibutyryl-cGMP, Upregulation of IL-8 release by NO was associated with increased IL-8 mRNA levels (P = .009). These data suggest that NO does not directly affect neutrophil chemotaxis but may indirectly alter chemotactic responses by increasing IL-8 production via a cGMP-independent pathway.
引用
收藏
页码:116 / 126
页数:11
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