Superoxide production in human neutrophils: Evidence for signal redundancy and the involvement of more than one PKC isoenzyme class

被引:34
作者
Pongracz, J [1 ]
Lord, JM [1 ]
机构
[1] Univ Birmingham, Sch Med, Dept Immunol, Birmingham B15 2TT, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1006/bbrc.1998.8867
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
Selective protein kinase C (PKC) activators and inhibitors and a physiological agonist, fMLP, were used to study superoxide production and PKC isoenzyme activation in human neutrophils. The data show that the classical PKC isoenzymes, alpha and beta, were activated by TPA and at a time prior to NADPH oxidase complex assembly. fMLP induced activation of PKC-beta over a similar time course. Inhibition of c-PKCs reduced, but did not block, TPA-induced superoxide production completely, suggesting additional PKC isoenzymes were involved beyond NADPH oxidase assembly. PKC inhibitors were unable to inhibit fMLP-induced superoxide generation, indicative of signal redundancy in the induction of superoxide generation in human neutrophils. (C) 1998 Academic Press.
引用
收藏
页码:624 / 629
页数:6
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