ROS-deficient monocytes have aberrant gene expression that correlates with inflammatory disorders of chronic granulomatous disease

被引:57
作者
Brown, Kelly L. [1 ]
Bylund, Johan [2 ]
MacDonald, Kelly L. [2 ]
Song-Zhao, George X. [1 ]
Elliott, Melissa R. [1 ]
Falsafi, Reza [1 ]
Hancock, Robert E. W. [1 ]
Speert, David P. [1 ,2 ]
机构
[1] Univ British Columbia, Dept Microbiol & Immunol, Ctr Microbial Dis Res, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada
基金
瑞典研究理事会;
关键词
inflammation; gene regulation; cytokines; lipopolysaccharide; reactive oxygen species;
D O I
10.1016/j.clim.2008.06.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic granulomatous disease is an immunodeficiency caused by an inability to produce reactive oxygen species, While the mechanism of hyper-sensitivity to infection is well understood in CGD, the basis for debilitating inflammatory disorders that arise in the absence of evident infection has not been fully explained. Herein it is demonstrated that resting and TLR-activated monocytes from individuals with CGD expressed significantly higher levels of inflammatory mediators than control cells; the expression in CGD cells resembled normal cells stimulated with lipopolysaccharide. The tack of acute illness, infection or circulating endotoxin in the blood of the CGD patients at the time of sampling was consistent with infection-free inflammation. The enhanced expression of inflammatory mediators correlated with elevated expression of NF-kappa B and was dependent on ERK1/2 signalling. The results are consistent with the hypothesis that ROS are anti-inflammatory mediators that control gene expression and potentially limit the development of sterile inflammatory disorders. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:90 / 102
页数:13
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