Goureau O, Hicks D, Courtois Y
Unité de Recherches Gérontologiques, INSERM U 118, Association Claude Bernard, Paris, France.
Biochem Biophys Res Commun. 1994 Jan 14;198(1):120-6. doi: 10.1006/bbrc.1994.1017.
The present study demonstrates that human retinal pigmented epithelial cells produce nitric oxide (NO) upon co-treatment with interferon gamma (IFN gamma) and interleukin-1 beta (IL-1 beta). The biosynthesis of NO, which was measured by the accumulation of the stable end-product nitrite, requires an induction period of approximately 12 hours and continues for at least three days. The synthesis was abolished by the stereoselective inhibitors of NO synthase (NOS), NG-monomethyl-L-arginine, N omega-nitro-L-arginine and N omega-nitro-L-arginine methyl ester and by cycloheximide. Transforming growth factor beta suppressed cytokine-induced NOS. The results indicate that cytokines such as IFN gamma and IL-1 beta are capable of inducing NOS, while TGF beta prevents this induction, in subcultured pigmented epithelial cells from the human retina.
本研究表明,人视网膜色素上皮细胞在与干扰素γ(IFNγ)和白细胞介素-1β(IL-1β)共同处理后会产生一氧化氮(NO)。通过稳定终产物亚硝酸盐的积累来测量的NO生物合成需要约12小时的诱导期,并持续至少三天。NO合酶(NOS)的立体选择性抑制剂NG-单甲基-L-精氨酸、Nω-硝基-L-精氨酸和Nω-硝基-L-精氨酸甲酯以及环己酰亚胺可消除该合成。转化生长因子β抑制细胞因子诱导的NOS。结果表明,在来自人视网膜的传代培养色素上皮细胞中,诸如IFNγ和IL-1β等细胞因子能够诱导NOS,而TGFβ可阻止这种诱导。