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Candida albicans suppresses nitric oxide (NO) production by interferon-gamma (IFN-γ) and lipopolysaccharide (LPS)-stimulated murine peritoneal macrophages

机译:白色念珠菌可抑制干扰素-γ(IFN-γ)和脂多糖(LPS)刺激的小鼠腹膜巨噬细胞产生的一氧化氮(NO)。

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摘要

We examined the in vitro effect of Candida albicans on NO production by macrophages. Candida albicans suppressed not only NO production but also expression of inducible NO synthase (iNOS) mRNA by murine IFN-γ and bacterial LPS-stimulated peritoneal macrophages. The suppression was not associated with inhibition but rather stimulation of IL-1β production. This effect was observed when more than 1 × 103/ml of Candida albicans were added to macrophage cultures (1 × 106 cells/ml) and reached a maximal level at 1 × 106/ml. The NO inhibitory effect of Candida albicans was mediated predominantly by as yet unidentified soluble factor(s) and to a lesser extent by direct contact. In addition, heat- or paraformaldehyde-killed Candida albicans did not show this inhibitory activity. Culture supernatant of Candida albicans also inhibited NO production by activated macrophages in a dose-dependent manner, and increased IL-1β production. Finally, the inhibitory effect was not mediated by IL-10 and transforming growth factor-beta (TGF-β), since neutralizing antibodies to these cytokines did not influence Candida albicans-induced reduction in macrophage NO production. Our results suggest that Candida albicans may evade host defence mechanism(s) through a soluble factor-mediated suppression of NO production by stimulated macrophages, and that the effect is independent of production of immunosuppressive cytokines such as IL-10 and TGF-β.
机译:我们检查了白色念珠菌对巨噬细胞产生NO的体外作用。白色念珠菌不仅抑制了NO的产生,而且抑制了鼠IFN-γ和细菌LPS刺激的腹膜巨噬细胞诱导型NO合酶(iNOS)mRNA的表达。抑制与抑制无关,而与IL-1β产生的刺激有关。当将大于1×10 3 / ml的白色念珠菌添加到巨噬细胞培养物中(1×10 6 细胞/ ml)并达到最大水平时,观察到这种效果。 1×10 6 / ml。白色念珠菌的NO抑制作用主要是由尚未确定的可溶性因子介导的,在较小程度上是通过直接接触介导的。另外,热或低聚甲醛杀死的白色念珠菌没有显示这种抑制活性。白色念珠菌的培养物上清液也以剂量依赖的方式抑制了活化巨噬细胞的NO产生,并增加了IL-1β的产生。最后,抑制作用不是由IL-10和转化生长因子-β(TGF-β)介导的,因为针对这些细胞因子的中和抗体不会影响白色念珠菌诱导的巨噬细胞NO生成减少。我们的结果表明,白色念珠菌可能通过可溶性因子介导的受刺激巨噬细胞对NO产生的抑制作用来逃避宿主防御机制,并且该作用独立于免疫抑制细胞因子(如IL-10和TGF-β)的产生。

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