Institute of Clinical Medicine, School ofMedicine, National Yang-Ming University, Taipei, Taiwan.
Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6832-41. doi: 10.1167/iovs.11-7815.
Genetic variation in complement factor H (CFH) has been implicated as a major risk factor for age-related macular degeneration (AMD). The reduction in CFH amount or its complement-modulating activity may lead to inadequate control of complement-driven inflammation at the outer retina. We explored the effect of photo-oxidative stress and inflammatory cytokine on the expression of CFH in retinal pigment epithelial (RPE) cells.
Cultured human RPE cells were exposed to blue light in the presence of interferon-γ (IFN-γ). CFH expression in cell lysate was examined by Western blot and the secretory CFH in culture medium was analyzed by ELISA. RPE cells were treated with vitamin C and exogenous superoxide dismutase mimetic (Tempol) before photo-oxidative treatments. The intracellular reactive oxygen species were examined by flow cytometry.
IFN-γ increased CFH expression in RPE and the expression was suppressed significantly under concomitant blue light illumination. The secretory CFH level also decreased significantly under blue light illumination, which was related to the decreased intracellular mRNA and protein expressions of CFH. The suppression was mediated through an oxidative mechanism, and was particularly related to superoxide anion generation. The suppression of CFH expression in RPE under blue light illumination was abrogated by vitamin C and Tempol.
Photo-oxidative stress reduces the ability of IFN-γ to increase CFH expression in RPE. Apart from reducing the oxidative damage, vitamin C reduces the suppression of CFH under photo-oxidative stress. These results suggest a new perspective of the interaction between oxidative stress and inflammation, and provide a potential novel treatment strategy for age-related macular degeneration.
补体因子 H(CFH)的遗传变异被认为是年龄相关性黄斑变性(AMD)的主要危险因素。CFH 数量或其补体调节活性的减少可能导致对外层视网膜补体驱动的炎症的控制不足。我们探讨了光氧化应激和炎症细胞因子对视网膜色素上皮(RPE)细胞 CFH 表达的影响。
培养的人 RPE 细胞在存在干扰素-γ(IFN-γ)的情况下暴露于蓝光下。通过 Western blot 检测细胞裂解物中 CFH 的表达,通过 ELISA 分析培养上清液中分泌型 CFH。在光氧化处理之前,用维生素 C 和外源性超氧化物歧化酶模拟物(Tempol)处理 RPE 细胞。通过流式细胞术检测细胞内活性氧物种。
IFN-γ增加了 RPE 中的 CFH 表达,并且在伴随的蓝光照射下表达显著受到抑制。在蓝光照射下,分泌型 CFH 水平也显著降低,这与 CFH 的细胞内 mRNA 和蛋白表达减少有关。这种抑制是通过氧化机制介导的,与超氧阴离子的产生特别相关。维生素 C 和 Tempol 可消除蓝光照射下 RPE 中 CFH 表达的抑制。
光氧化应激降低了 IFN-γ 增加 RPE 中 CFH 表达的能力。除了减少氧化损伤外,维生素 C 还减少了光氧化应激下 CFH 的抑制。这些结果为氧化应激和炎症之间的相互作用提供了一个新的视角,并为年龄相关性黄斑变性提供了一种潜在的新的治疗策略。