Berkman N, Robichaud A, Robbins R A, Roesems G, Haddad E B, Barnes P J, Chung K F
Department of Thoracic Medicine, National Heart & Lung Institute, Imperial College of Science, Technology & Medicine, London, UK.
Immunology. 1996 Nov;89(3):363-7. doi: 10.1046/j.1365-2567.1996.d01-745.x.
Nitric oxide produced by the inducible enzyme, nitric oxide synthase (iNOS), is implicated in immunological and inflammatory processes. We determined the effects of T-helper (Th)2-derived cytokines on the induction of iNOS from an epithelial A549 cell line and human airway epithelial cells stimulated by a mixture of interleukin-1 beta (IL-1 beta), interferon-gamma (IFN-gamma) and tumour necrosis factor-alpha (TNF-alpha). Interleukin-4 (IL-4) and interleukin-13 (IL-13) but not interleukin-10 (IL-10) inhibited both iNOS mRNA expression and nitrite release in A549 cells. On human airway epithelial cells, IL-4 and IL-13 reduced iNOS mRNA expression. Dexamethasone also inhibited both iNOS expression and nitrite release. Th2 cytokines, IL-4 and IL-13, inhibit iNOS upregulation by Th1 cytokines, indicating an important reciprocal role of Th1 and Th2 T-cell subsets on lung epithelial cells.
由诱导型酶一氧化氮合酶(iNOS)产生的一氧化氮与免疫和炎症过程有关。我们测定了辅助性T细胞2(Th2)衍生的细胞因子对上皮A549细胞系和受到白细胞介素-1β(IL-1β)、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)混合物刺激的人气道上皮细胞中iNOS诱导的影响。白细胞介素-4(IL-4)和白细胞介素-13(IL-13)而非白细胞介素-10(IL-10)抑制了A549细胞中iNOS mRNA的表达和亚硝酸盐的释放。在人气道上皮细胞上,IL-4和IL-13降低了iNOS mRNA的表达。地塞米松也抑制了iNOS的表达和亚硝酸盐的释放。Th2细胞因子IL-4和IL-13抑制Th1细胞因子对iNOS的上调作用,表明Th1和Th2 T细胞亚群在肺上皮细胞上具有重要的相互作用。