STAUROSPORINE INHIBITS THE SOLUBLE AND MEMBRANE-BOUND PROTEIN TYROSINE KINASES OF HUMAN NEUTROPHILS

被引:67
作者
BADWEY, JA
ERICKSON, RW
CURNUTTE, JT
机构
[1] HARVARD UNIV, SCH MED, DEPT BIOL CHEM & MOLEC PHARMACOL, BOSTON, MA 02115 USA
[2] Scripps Res Inst, RES INST, DEPT MOLEC & EXPTL MED, LA JOLLA, CA 92037 USA
关键词
PHOSPHATASE-ACTIVITY; RESPIRATORY BURST; POLYMORPHONUCLEAR LEUKOCYTES; SUPEROXIDE PRODUCTION; SIGNAL TRANSDUCTION; PHOSPHORYLATION; ACTIVATION; INSULIN; CELLS; STIMULATION;
D O I
10.1016/0006-291X(91)90124-P
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
Superoxide production by neutrophils triggered with a chemotactic peptide or a phorbol ester is inhibited by the protein kinase antagonists staurosporine or 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine (H-7). We evaluated the effects of these antagonists on the protein tyrosine kinases and protein kinase C activities of neutrophils. Staurosporine completely inhibited all of these enzymes, whereas 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine was only substantially effective against protein kinase C. Thus, if a protein tyrosine kinase is involved in superoxide production, it is likely to function with a second kinase sensitive to 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine. © 1991.
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页码:423 / 429
页数:7
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