首页> 外文期刊>Research in Microbiology >Role of Pasteurella multocida, Pasteurella haemolytica and Salmonella typhimurium porins on inducible nitric oxide release by murine macrophages.
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Role of Pasteurella multocida, Pasteurella haemolytica and Salmonella typhimurium porins on inducible nitric oxide release by murine macrophages.

机译:多杀性巴斯德氏菌,溶血巴斯德氏菌和鼠伤寒沙门氏菌孔蛋白对鼠巨噬细胞诱导型一氧化氮释放的作用。

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The aim of this study was to verify whether Pasteurella haemolytica, P. multocida and Salmonella typhimurium porins could affect the inducible nitric oxide synthase (iNOS) expression and nitric oxide (NO) release by murine resident peritoneal macrophages in vitro. We also compared their effect with that elicited by P. haemolytica, P. multocida and S. typhimurium lipopolysaccharide (LPS) whose biological activity is well known. Variations in NO release and iNOS mRNA expression due to variable concentrations of porins were recorded and compared. We also investigated the synergism between bacterial products and interferon gamma (IFN-gamma). With this aim cells were incubated with porins together with murine rIFN-gamma prior to assessing the presence of NO in the supernatant and mRNA analysis. Porins in themselves were not able to induce NO release by resident peritoneal macrophages. Incubation of macrophages with IFN-gamma in the presence of porins increased NO release, whereas incubation in the presence of the arginine analog N(G)-monomethyl-L-arginine (NMA) inhibited NO release. The greatest NO release was obtained using porins at a concentration of 5 microg/mL. Porins, together with IFN-gamma, were also able to upregulate the mRNA expression of iNOS. Our findings suggest that gram-negative porins are able to modulate inflammatory and immunological responses by affecting the release of NO and the expression of iNOS gene in activated macrophages.
机译:这项研究的目的是验证溶血巴斯德氏菌,多杀性巴氏杆菌和鼠伤寒沙门氏菌孔蛋白是否能在体外影响鼠类常驻腹膜巨噬细胞的诱导型一氧化氮合酶(iNOS)表达和一氧化氮(NO)释放。我们还比较了它们的作用与溶血性疟原虫,多杀性疟原虫和鼠伤寒沙门氏菌脂多糖(LPS)引起的生物学活性众所周知的作用。记录并比较了由于孔蛋白浓度不同而导致的NO释放和iNOS mRNA表达的变化。我们还研究了细菌产物和干扰素γ(IFN-γ)之间的协同作用。为此目的,将细胞与孔蛋白以及鼠rIFN-γ一起孵育,然后评估上清液中是否存在NO和mRNA分析。孔蛋白本身不能诱导常驻腹膜巨噬细胞释放NO。在存在孔蛋白的情况下,将巨噬细胞与IFN-γ一起孵育可增加NO的释放,而在精氨酸类似物N(G)-单甲基-L-精氨酸(NMA)的存在下孵育可抑制NO的释放。使用孔蛋白浓度为5 microg / mL可获得最大的NO释放量。孔蛋白与IFN-γ一起也能够上调iNOS的mRNA表达。我们的发现表明,革兰氏阴性孔蛋白能够通过影响活化巨噬细胞中NO的释放和iNOS基因的表达来调节炎症反应和免疫反应。

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