Tucková L, Flegelová Z, Tlaskalová-Hogenová H, Zídek Z
Institute of Microbiology, Academy of Sciences of the Czech Republic, Prague.
J Leukoc Biol. 2000 Mar;67(3):312-8. doi: 10.1002/jlb.67.3.312.
Macrophages play an important role in effector mechanisms of various chronic inflammatory diseases. We studied the effect of gluten, the agent inducing celiac disease, and other food antigens on the activation of macrophages. Nitric oxide (NO) and cytokine production were followed as markers of activation, using cultured murine peritoneal macrophages. None of the food antigens tested caused direct inducible nitric oxide synthase (iNOS) activation in macrophages. Unlike other food antigens gluten, gliadin, and their proteolytic fragments significantly enhanced NO production when applied together with interferon-gamma (IFN-gamma), the most efficient being fragments originating from 25- to 45-min peptic digestion. The activation pathway was mediated via direct stimulation of tumor necrosis factor alpha (TNF-alpha) secretion. The NO-enhancing effect was confirmed at the level of iNOS mRNA transcription. In case of sustained local inflammatory reaction connected with increase of IFN-gamma, gluten and its proteolytic fragments may thus elevate NO production. Increased NO level could consequently participate in the development of mucosal lesions in the gut of celiac patients.
巨噬细胞在各种慢性炎症性疾病的效应机制中发挥着重要作用。我们研究了麸质(引发乳糜泻的因子)及其他食物抗原对巨噬细胞激活的影响。以培养的小鼠腹腔巨噬细胞为研究对象,跟踪检测一氧化氮(NO)和细胞因子的产生情况,以此作为激活的标志物。所测试的食物抗原均未直接导致巨噬细胞中诱导型一氧化氮合酶(iNOS)激活。与其他食物抗原不同,麸质、麦醇溶蛋白及其蛋白水解片段与γ干扰素(IFN-γ)共同作用时,能显著增强NO的产生,其中最有效的是源自胃蛋白酶消化25至45分钟的片段。激活途径是通过直接刺激肿瘤坏死因子α(TNF-α)的分泌介导的。在iNOS mRNA转录水平也证实了NO增强效应。因此,在与IFN-γ增加相关的持续性局部炎症反应情况下,麸质及其蛋白水解片段可能会提高NO的产生。NO水平升高可能会参与乳糜泻患者肠道黏膜病变的发展。