SP-D-dependent regulation of NO metabolism in lipopolysaccharide-stimulated peritoneal macrophages

Bull Exp Biol Med. 2009 Apr;147(4):415-20. doi: 10.1007/s10517-009-0525-z.
[Article in English, Russian]

Abstract

This work was designed to study the role of surfactant protein D in the regulation of NO synthesis by "non-alveolar" microphages. We evaluated whether the effects of surfactant protein D depend on the phenotype of macrophages. In the absence of surfactant protein D, the LPS-induced iNOS response was shown to decrease in macrophages of native and proinflammatory phenotypes by 30%, and in macrophages of the antiinflammatory phenotype (by 63%). Under the influence of lipopolysaccharide in high doses (500 ng/ml), NO(2)*- production by mouse macrophages without surfactant protein D was reduced in native cells (by 25%), but increased in proinflammatory (by 40%) and antiinflammatory phenotypes (by 12% compared to mouse macrophages with surfactant protein D). Our results suggest that surfactant protein D is involved in the immune response in the whole organism, but not only in the lungs. The effect of surfactant protein D depends on the phenotype of macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cytokines / metabolism
  • Lipopolysaccharides / toxicity*
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase Type II / metabolism
  • Nitrites / metabolism
  • Peritoneal Cavity / cytology
  • Peritoneal Cavity / physiopathology*
  • Pulmonary Surfactant-Associated Protein D / genetics
  • Pulmonary Surfactant-Associated Protein D / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors

Substances

  • Cytokines
  • Lipopolysaccharides
  • Nitrites
  • Pulmonary Surfactant-Associated Protein D
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse