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Differential expression of inducible nitric oxide synthase gene by alveolar and peritoneal macrophages in lipopolysaccharide‐hyporesponsive C3H/HeJ mice

机译:脂多糖低反应性C3H / HeJ小鼠肺泡和腹膜巨噬细胞诱导型一氧化氮合酶基因的差异表达

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摘要

In lipopolysaccharide (LPS)‐hyporesponsive C3H/HeJ mice, alveolar macrophages (AMφ) produce much more tumour necrosis factor‐α than peritoneal macrophages (PMφ) when stimulated with LPS (10 µg/ml), but the induction of inducible nitric oxide synthase (iNOS) gene expression and production of nitric oxide (NO) in AMφ are not found. In the present study, we determined the induction of iNOS gene expression, using semi‐quantitative reverse transcription–polymerase chain reaction, and the release of NO in AMφ and PMφ from C3H/HeJ and C3H/HeN mice. The results showed the induction of iNOS mRNA accumulation in a dose‐dependent manner by LPS alone or in combination with interferon‐γ in both macrophages. The effects of the stimuli on iNOS gene expression and NO production were significantly higher in AMφ than in the PMφ of C3H/HeJ mice. The response of macrophages from C3H/HeN mice was similar to those from C3H/HeJ mice, but the difference of iNOS gene expression between AMφ and PMφ in C3H/HeN mice was not as striking as in C3H/HeJ mice. The results show that the iNOS gene expression and NO production were activated differently in AMφ and PMφ and suggest that the functional properties of macrophages isolated from distinct origins are different.
机译:在脂多糖(LPS)低反应性C3H / HeJ小鼠中,当用LPS(10 µg / ml)刺激时,肺泡巨噬细胞(AMφ)产生的肿瘤坏死因子-α比腹膜巨噬细胞(PMφ)多得多,但诱导型一氧化氮合酶的诱导找不到AMφ中的(iNOS)基因表达和一氧化氮(NO)的产生。在本研究中,我们使用半定量逆转录聚合酶链反应确定了iNOS基因表达的诱导作用,并确定了C3H / HeJ和C3H / HeN小鼠AMφ和PMφ中NO的释放。结果表明,在两个巨噬细胞中,LPS单独或与干扰素-γ联合诱导iNOS mRNA积累呈剂量依赖性。刺激对AMφ的iNOS基因表达和NO产生的影响显着高于C3H / HeJ小鼠的PMφ。 C3H / HeN小鼠的巨噬细胞反应与C3H / HeJ小鼠相似,但是C3H / HeN小鼠AMφ和PMφ之间iNOS基因表达的差异不如C3H / HeJ小鼠明显。结果表明,在AMφ和PMφ中,iNOS基因的表达和NO产生被不同地激活,这表明从不同来源分离的巨噬细胞的功能特性是不同的。

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