Regulation of leukotriene B4 generation from human polymorphonuclear granulocytes after stimulation with formyl-methionyl-leucyl phenylalanine: effects of pertussis and cholera toxins

Infect Immun. 1991 Sep;59(9):3046-52. doi: 10.1128/iai.59.9.3046-3052.1991.

Abstract

The effects of holotoxins and toxin subunits from Bordetella pertussis and Vibrio cholerae strains on intact and digitonin-permeabilized human polymorphonuclear neutrophils were studied. Our data clearly demonstrate that formyl-methionyl-leucyl-phenylalanine (fMLP)-induced generation of chemotactic active leukotriene B4 was inhibited by both holotoxins as well as by their isolated enzymatic A protomers. In contrast, the respective binding components (B oligomers) did not affect leukotriene formation. Priming of digitonin-permeabilized neutrophils with either guanylylimidodiphosphate or inositol trisphosphate increased subsequent stimulation with fMLP. In contrast, diacylglycerol decreased fMLP-induced leukotriene B4 formation, but inositol trisphosphate and diacylglycerol had no effect on inhibition mediated by the toxins. In addition, pertussis and cholera toxins reduced the specific binding of [3H]fMLP. Scatchard plot analysis revealed that the observed decrease of peptide binding was due to a reduced number of receptor sites. The fMLP-stimulated [3H]guanylylimidodiphosphate binding and GTPase activity used as parameters for the activation of G proteins were decreased in parallel. These results suggest altered chemotactic receptor numbers and G-protein functions responsible for the toxin-dependent suppression of fMLP-mediated response for neutrophils.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cholera Toxin / pharmacology*
  • GTP-Binding Proteins / immunology
  • GTP-Binding Proteins / metabolism
  • Humans
  • Leukotriene B4 / immunology*
  • N-Formylmethionine Leucyl-Phenylalanine / pharmacology*
  • Neutrophils / immunology*
  • Neutrophils / metabolism
  • Permeability
  • Phosphatidylinositols / immunology
  • Phosphatidylinositols / metabolism
  • Receptors, Formyl Peptide
  • Receptors, Immunologic / immunology
  • Signal Transduction
  • Virulence Factors, Bordetella / pharmacology*

Substances

  • Phosphatidylinositols
  • Receptors, Formyl Peptide
  • Receptors, Immunologic
  • Virulence Factors, Bordetella
  • Leukotriene B4
  • N-Formylmethionine Leucyl-Phenylalanine
  • Cholera Toxin
  • GTP-Binding Proteins