MODIFICATION OF NEUTROPHIL OXIDANT PRODUCTION WITH DIPHENYLENEIODONIUM AND ITS EFFECT ON BACTERIAL KILLING

被引:60
作者
HAMPTON, MB
WINTERBOURN, CC
机构
[1] Free Radical Research Unit, Department of Pathology, Christchurch School of Medicine, Christchurch
关键词
NEUTROPHILS; BACTERIAL KILLING; OXIDANTS; FREE RADICALS;
D O I
10.1016/0891-5849(94)00181-I
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
Diphenyleneiodonium (DPI), an inhibitor of the NADPH oxidase, has been used to distinguish between oxidative and nonoxidative killing of Staphylococcus aureus and Escherichia coli by neutrophils. The rate of killing of S. aureus was inhibited by 77% in the presence of 10 mu M DPI, compared to 81% measured under anaerobic conditions. DPI represents a convenient and accessible alternative to an anaerobic environment or using neutrophils from patients with chronic granulomatous disease, for eliminating oxidative killing. The killing of E. coli was also inhibited by DPI. The effect was more apparent at 30 min than at 10 min, suggesting that E. coli can be killed rapidly by nonoxidative mechanisms that become less efficient at later times. DPI was used at concentrations less than 10 mu M to determine how this affected production of the three major neutrophil oxidants, superoxide, hydrogen peroxide, and hypochlorous acid, and to determine the effect of partial inhibition of oxidant production on the killing of S. aureus. Unexpectedly, lower concentrations of DPI (0.1-2 mu M) inhibited hydrogen peroxide and hypochlorous acid production 10-30% more than they inhibited superoxide production. Correlation of hydrogen peroxide or hypochlorous acid production with the killing of S. aureus showed that up to 30% inhibition had no effect on the rate of killing, implying that agents that impair neutrophil oxidant production less than this will not compromise bacterial killing. Higher inhibition of oxidant production led to a linear decline in the rate of killing.
引用
收藏
页码:633 / 639
页数:7
相关论文
共 34 条
[1]   BIOLOGICAL DEFENSE MECHANISMS - PRODUCTION BY LEUKOCYTES OF SUPEROXIDE A POTENTIAL BACTERICIDAL AGENT [J].
BABIOR, BM ;
KIPNES, RS ;
CURNUTTE, JT .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (03) :741-744
[2]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[3]   IS THERE ANY SPECIFICITY TO DEFECTS OF ANCHORING FIBRILS IN EPIDERMOLYSIS BULLOSA DYSTROPHICA, AND WHAT DOES THIS MEAN IN TERMS OF PATHOGENESIS [J].
BRIGGAMAN, RA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1985, 84 (05) :371-373
[4]   THE EFFECT OF THE INHIBITOR DIPHENYLENE IODONIUM ON THE SUPEROXIDE-GENERATING SYSTEM OF NEUTROPHILS - SPECIFIC LABELING OF A COMPONENT POLYPEPTIDE OF THE OXIDASE [J].
CROSS, AR ;
JONES, OTG .
BIOCHEMICAL JOURNAL, 1986, 237 (01) :111-116
[5]   THE EFFECT OF THE NADPH OXIDASE INHIBITOR DIPHENYLENEIODONIUM ON AEROBIC AND ANAEROBIC MICROBICIDAL ACTIVITIES OF HUMAN-NEUTROPHILS [J].
ELLIS, JA ;
MAYER, SJ ;
JONES, OTG .
BIOCHEMICAL JOURNAL, 1988, 251 (03) :887-891
[6]  
Elsbach P., 1988, INFLAMMATION BASIC P, P445
[7]  
FOREHAND JR, 1989, METABOLIC BASIS INHE, P2779
[8]   KINETICS AND MECHANISM OF THE BACTERICIDAL ACTION OF HUMAN-NEUTROPHILS AGAINST ESCHERICHIA-COLI [J].
HAMERS, MN ;
BOT, AAM ;
WEENING, RS ;
SIPS, HJ ;
ROOS, D .
BLOOD, 1984, 64 (03) :635-641
[9]   A SINGLE ASSAY FOR MEASURING THE RATES OF PHAGOCYTOSIS AND BACTERIAL KILLING BY NEUTROPHILS [J].
HAMPTON, MB ;
VISSERS, MCM ;
WINTERBOURN, CC .
JOURNAL OF LEUKOCYTE BIOLOGY, 1994, 55 (02) :147-152
[10]  
Klebanoff SJ., 1988, INFLAMMATION BASIC P, P391