Abstract
The interaction of cytochalasin B-treated human neutrophils with the synthetic tripeptide, N-formyl-methionyl-leucyl-phenylalanine (FMLP) results in a time- and concentration-dependent generation of superoxide anion (O2-) by an extracellular release of granule-associated beta-glucuronidase and lysozyme from these cells. Granule exocytosis was not accompanied by significant cytoplasmic lactate dehydrogenase extrusion. FMLP-stimulated O2- production occurs but is significantly curtailed in the absence of extracellular calcium. Nevertheless, incubation of neutrophils with EGTA in calcium-free medium had no effect on the O2- -generating system. Trifluoperazine (TFP), an inhibitor of calmodulin (a calcium-binding protein), caused a dose-related inhibition of FMLP-elicited degranulation and O2- production in the presence of absence of extracellular calcium. This effect TFP could be reversed by washing the cells before contact with FMLP. These data suggest that TFP represents a useful tool for defining the relevance of calmodulin and calcium to neutrophil function.
MeSH Terms
Cells, Cultured
Cytochalasin B/pharmacology
Cytoplasmic Granules/drug effects,enzymology
Dose-Response Relationship, Drug
Exocytosis/drug effects
Humans
N-Formylmethionine/analogs & derivatives,pharmacology
N-Formylmethionine Leucyl-Phenylalanine
Neutrophils/drug effects,metabolism
Oligopeptides/pharmacology
Superoxides/metabolism
Trifluoperazine/pharmacology
Chemicals
Oligopeptides
Superoxides
Trifluoperazine
Cytochalasin B
N-Formylmethionine
N-Formylmethionine Leucyl-Phenylalanine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Smith R J
Bowman B J
Iden S S
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