Pharmacological analysis for mechanisms of GPI-80 release from tumour necrosis factor-alpha-stimulated human neutrophils

Br J Pharmacol. 2002 Oct;137(3):353-60. doi: 10.1038/sj.bjp.0704860.

Abstract

1 GPI-80, a glycosylphosphatidylinositol (GPI)-anchored protein initially identified on human neutrophils, plays a role(s) in the regulation of beta2 integrin function. Previous studies have shown that GPI-80 is sublocated in secretory vesicles. It is also found in soluble form in the synovial fluid of rheumatoid arthritis patients, and in the culture supernatant of formyl-methionyl-leucyl-phenylalanine-stimulated neutrophils. To understand the behaviour of GPI-80 under conditions of stimulation, we investigated the effects of tumour necrosis factor (TNF)-alpha on its expression and release. We also probed the mechanism of its release with various pharmacologic tools. 2 TNF-alpha induced the release of GPI-80 from human neutrophils in a concentration- and time-dependent manner (in the range of 1-100 u ml(-1) and 30-120 min, respectively), but did not affect surface GPI-80 levels. 3 Cytochalasin B, genistein, and SB203580 but not PD98059 inhibited TNF-alpha-stimulated GPI-80 release and neutrophil adherence at the same concentration. In addition, TNF-alpha-induced GPI-80 release was inhibited by blocking monoclonal antibodies specific to components of Mac-1 (CD11b and CD18). 4 Antioxidants (pyrrolidine dithiocarbamate and N-acetyl-L-cysteine) inhibited GPI-80 release by TNF-alpha stimulation, but superoxide dismutase did not. Antioxidants but not superoxide dismutase reduced an intracellular oxidation state. 5 These findings indicate that TNF-alpha-stimulated GPI-80 release from human neutrophils depends upon adherence via beta2 integrins. They also suggest that cytochalasin B, genistein, and SB203580 inhibit GPI-80 release by suppressing signals for cell adherence, rather than by a direct effect on its secretion. Finally, we suggest that GPI-80 release involves an intracellular change in a redox state.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases
  • Antioxidants / pharmacology
  • CD18 Antigens / metabolism
  • Cell Adhesion
  • Cell Adhesion Molecules / biosynthesis*
  • Cytochalasin B / pharmacology
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Flavonoids / pharmacology
  • GPI-Linked Proteins
  • Genistein / pharmacology
  • Humans
  • Hydrolases
  • Imidazoles / pharmacology
  • In Vitro Techniques
  • Neutrophil Activation
  • Neutrophils / drug effects*
  • Neutrophils / metabolism
  • Neutrophils / physiology
  • Pyridines / pharmacology
  • Structure-Activity Relationship
  • Time Factors
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Antioxidants
  • CD18 Antigens
  • Cell Adhesion Molecules
  • Enzyme Inhibitors
  • Flavonoids
  • GPI-Linked Proteins
  • Imidazoles
  • Pyridines
  • Tumor Necrosis Factor-alpha
  • Cytochalasin B
  • Genistein
  • Hydrolases
  • Amidohydrolases
  • VNN2 protein, human
  • SB 203580
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one