Most cited article - PubMed ID 10975603
Genetic variation in in-vitro cytokine-induced production of nitric oxide by murine peritoneal macrophages
The effect of nonpathogenic G+ bacterium B. firmus (BF) on stimulation of mouse peritoneal cells in vitro was evaluated by testing nitric-oxide-synthesis induction and cytokine formation. The reactivity was compared of peritoneal cells from two inbred mouse strains, C57B1/6 and BALB/c, which differ in their immunological reactivity. Peritoneal macrophages from C57B1/6 produced more nitric oxide after a 1-d cultivation with inactivated BF than those of BALB/c mice. In both strains, production can be further increased by adding exogenous IFN-gamma to the culture. There were no significant differences between peritoneal cells of these two mouse strains in cytokine production after optimal in vitro stimulation with BF. BF effectively activated peritoneal cells for the production of TNF-alpha, IL-1beta and IL-10, delipidated bacterium (DBF) being more efficient than BF in induction of IL-10 and TNF-alpha. On the other hand, BF had only small effect on IFN-gamma production and no detectable effect on IL-12 production. Macrophage activation by BF/DBF can represent one of the mechanisms responsible for previously described immunomodulatory activity of BF.
- MeSH
- Macrophage Activation * MeSH
- Bacillus immunology MeSH
- Cell Culture Techniques methods MeSH
- Cytokines immunology metabolism MeSH
- Lipopolysaccharides pharmacology MeSH
- Mice, Inbred BALB C MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Organic Chemicals pharmacology MeSH
- Nitric Oxide metabolism MeSH
- Peritoneal Cavity cytology MeSH
- Immunity, Innate MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Cytokines MeSH
- Lipopolysaccharides MeSH
- Nocardia delipidated cell mitogen MeSH Browser
- Organic Chemicals MeSH
- Nitric Oxide MeSH