Mouse macrophages release a neutrophil chemotactic mediator following stimulation by staphylococcal enterotoxin type A

Inflamm Res. 2001 Apr;50(4):206-12. doi: 10.1007/s000110050745.

Abstract

Objective and design: To examine the role of macrophages in the neutrophil migration induced by staphylococcal enterotoxin type A (SEA) in mice.

Materials and methods: Peritoneal macrophages were harvested from male Swiss mice pre-treated with thioglycollate. After adhering to plastic tissue culture dishes, the cells were washed and incubated with RPMI or SEA (0.62-2.5 microg/ml) and washed again prior to further incubation with RPMI alone. The medium was then collected, sterilized and assayed for promigratory activity in the mouse peritoneal cavity.

Results: Mouse macrophage monolayers stimulated with SEA secreted a thermolabile neutrophil chemotactic component (MNCC-SEA) with a molecular mass >100 kDa (by ultrafiltration). This release was dose- and time-dependent and was inhibited by dexamethasone but not by indomethacin or BW755C. Dexamethasone, indomethacin, BWA4C, BW755C, BN52021, cimetidine and SR48968 had no effect on the neutrophil migration induced by MNCC-SEA while capsaicin and SR 140333 reduced this phenomenon.

Conclusions: Macrophages play a key role in the neutrophil recruitment induced by SEA probably by releasing an MNCC-SEA that presumably induces neutrophil migration via a mechanism mediated by substance P.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine / pharmacology
  • Animals
  • Benzamides / pharmacology
  • Calcium / pharmacology
  • Capsaicin / pharmacology
  • Chemotactic Factors / metabolism*
  • Chemotactic Factors / pharmacology
  • Chemotaxis, Leukocyte
  • Cyclooxygenase Inhibitors / pharmacology
  • Dexamethasone / pharmacology
  • Drug Stability
  • Enterotoxins / pharmacology*
  • Glucocorticoids / pharmacology
  • Glucose / pharmacology
  • Indomethacin / pharmacology
  • Macrophages, Peritoneal / metabolism*
  • Magnesium / pharmacology
  • Male
  • Mice
  • Molecular Weight
  • Neutrophils / physiology*
  • Piperidines / pharmacology
  • Receptors, Neurokinin-2 / antagonists & inhibitors
  • Thioglycolates / pharmacology

Substances

  • Benzamides
  • Chemotactic Factors
  • Cyclooxygenase Inhibitors
  • Enterotoxins
  • Glucocorticoids
  • Piperidines
  • Receptors, Neurokinin-2
  • Thioglycolates
  • enterotoxin A, Staphylococcal
  • 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine
  • SR 48968
  • Dexamethasone
  • Magnesium
  • Glucose
  • Capsaicin
  • Calcium
  • Indomethacin