Inducible nitric oxide synthase (NOS II) is constitutive in human neutrophils

被引:37
作者
Cedergren, J
Follin, P
Forslund, T
Lindmark, M
Sungqvist, T
Skogh, T
机构
[1] Linkoping Univ, Fac Hlth Sci, Dept Mol & Clin Med, Div Rheumatol, S-58183 Linkoping, Sweden
[2] Linkoping Univ, Fac Hlth Sci, Dept Mol & Clin Med, Div Infect Dis, S-58183 Linkoping, Sweden
[3] Linkoping Univ, Fac Hlth Sci, Dept Mol & Clin Med, Div Med Microbiol, S-58183 Linkoping, Sweden
关键词
inflammation; nitric oxide; iNOS; granulocytes;
D O I
10.1034/j.1600-0463.2003.1111008.x
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 objective was to study the expression of inducible nitric oxide synthase (NOS II) in and NO production by human blood neutrophils and in in vivo exudated neutrophils. Cellular expression of NOS II was evaluated by flow cytometry in whole blood, in isolated blood neutrophils, and in neutrophils obtained by exudation in vivo into skin chambers. Neutrophil NOS II was also demonstrated by Western blotting. Uptake of H-3-labelled L-arginine was studied in vitro and NOS activity measured in a whole cell assay by the conversion of H-3-arginine to H-3-citrulline. In contrast to unseparated blood cells, NOS II was demonstrable both in isolated blood neutrophils and exudated cells. The failure to detect NOS II by flow cytometry in whole blood cells thus proved to be due to the quenching effect of hemoglobin. Western blotting revealed a 130 kD band corresponding to NOS II in isolated blood neutrophils, but detection was dependent on diisopropylfluorophosphate for proteinase inhibition. L-arginine was taken up by neutrophils, but enzymatic activity could not be demonstrated. We conclude that human neutrophils constitutively express NOS II, but that its demonstration by FITC-labelling is inhibited by hemoglobin-mediated quenching in whole blood samples.
引用
收藏
页码:963 / 968
页数:6
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