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]
Affiliation
- 1 Russian Academy of Medical Sciences, Moscow, Russia.
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
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Cells, Cultured
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Cytokines / metabolism
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Lipopolysaccharides / toxicity*
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Macrophages / cytology
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Macrophages / drug effects*
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Macrophages / physiology*
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
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Nitric Oxide / metabolism*
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Nitric Oxide Synthase Type II / metabolism
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Nitrites / metabolism
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Peritoneal Cavity / cytology
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Peritoneal Cavity / physiopathology*
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Pulmonary Surfactant-Associated Protein D / genetics
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Pulmonary Surfactant-Associated Protein D / metabolism*
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Reverse Transcriptase Polymerase Chain Reaction
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Time Factors
Substances
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Cytokines
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Lipopolysaccharides
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Nitrites
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Pulmonary Surfactant-Associated Protein D
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Nitric Oxide
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Nitric Oxide Synthase Type II
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Nos2 protein, mouse