The change in leukotrienes and lipoxins in activated mouse peritoneal macrophages

Biochim Biophys Acta. 2000 Apr 12;1484(2-3):87-92. doi: 10.1016/s1388-1981(00)00015-9.

Abstract

The aim of this study was to investigate to what extent the generation of leukotrienes (LTs) and lipoxins (LXs) was affected by the expression of definite levels of macrophage activation. We used a system of murine peritoneal macrophages at different states of activation consisting in resident macrophages and FCS-, thioglycollate- or Corynebacterium parvum-elicited macrophages. The profile of lipoxygenase metabolites in resident macrophages was characterized by the presence of high levels of 12-HETE, followed by 15-HETE, 5-HETE, LTB(4) and 6-trans-LTB(4), 6-trans-12-epi-LTB(4). A comparable pattern was also found in FCS-elicited macrophages which appeared not to be responsive to the challenge with interferon gamma plus LPS, as measured by the generation of NO and tumor necrosis factor alpha. Resident as well as FCS-elicited macrophages also generated appreciable quantities of LXs (A(4) and B(4)). Thioglycollate-elicited macrophages, which expressed a state of 'responsive' macrophages, showed a block of the LT and LX synthesis. This block was also present in C. parvum-elicited macrophages which expressed a fully 'activated' phenotype, reflected by their capacity of releasing NO and tumor necrosis factor alpha even though they were not challenged. These results provide the first evidence that the level of 'responsive' as well as 'activated' macrophages was associated with of a simultaneous block of LTB(4) and LXs.

MeSH terms

  • Animals
  • Arachidonic Acids / metabolism*
  • Blood
  • Chromatography, High Pressure Liquid
  • Interferon-gamma
  • Leukotrienes / metabolism*
  • Lipopolysaccharides
  • Macrophage Activation
  • Macrophages, Peritoneal / metabolism*
  • Mice
  • Nitric Oxide / analysis
  • Propionibacterium acnes
  • Thioglycolates
  • Tumor Necrosis Factor-alpha / analysis

Substances

  • Arachidonic Acids
  • Leukotrienes
  • Lipopolysaccharides
  • Thioglycolates
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Interferon-gamma