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首页> 外文期刊>Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society >Progesterone inhibits inducible nitric oxide synthase gene expression and nitric oxide production in murine macrophages.
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Progesterone inhibits inducible nitric oxide synthase gene expression and nitric oxide production in murine macrophages.

机译:孕酮抑制鼠巨噬细胞中可诱导的一氧化氮合酶基因表达和一氧化氮生成。

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The purpose of this study was to determine whether the female hormones estradiol-l7 beta (E2) and progesterone (P4) influence inducible nitric oxide synthase (iNOS) and the production of nitric oxide (NO) by interferon-gamma(IFN-gamma)-and lipopolysaccharide (LPS)-activated mouse macrophages. Treatment with P4 alone caused a time- and dose-dependent inhibition of NO production by macrophage cell lines (RAW 264.7, J774) and mouse bone marrow culture-derived macrophages as assessed by nitrite accumulation. RAW 264.7 cells transiently transfected with an iNOS gene promoter/luciferase reporter-gene construct that were stimulated with IFN-gamma/LPS in the presence of P4 displayed reduced luciferase activity and NO production. Analysis of RAW 264.7 cells by Northern blot hybridization revealed concurrent P4-mediated reduction in iNOS mRNA. These observations suggest that P4-mediated inhibition of NO may be an important gender-based difference within females and males that relates to macrophage-mediated host defense.
机译:这项研究的目的是确定雌性激素雌二醇-17β(E2)和孕酮(P4)是否影响诱导型一氧化氮合酶(iNOS)和干扰素-γ(IFN-γ)产生一氧化氮(NO)和脂多糖(LPS)激活的小鼠巨噬细胞。单独用P4进行治疗会导致时间和剂量依赖性的巨噬细胞细胞系(RAW 264.7,J774)和小鼠骨髓培养物衍生的巨噬细胞对NO的产生产生抑制作用(通过亚硝酸盐积累评估)。在P4存在下用IFN-γ/ LPS刺激的iNOS基因启动子/荧光素酶报告基因构建体瞬时转染的RAW 264.7细胞显示出降低的荧光素酶活性和NO产生。通过Northern印迹杂交分析RAW 264.7细胞,发现iNOS mRNA同时存在P4介导的还原。这些观察结果表明,P4介导的NO抑制可能是雌性和雄性中基于性别的重要差异,这与巨噬细胞介导的宿主防御有关。

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