Garner B, Roberg K, Qian M, Eaton J W, Truscott R J
Australian Cataract Research Foundation, Department of Chemistry, University of Wollongong, NSW 2522, Australia.
Exp Eye Res. 2000 Dec;71(6):599-607. doi: 10.1006/exer.2000.0912.
Previous studies have shown that lenticular levels of Fe and Cu are elevated in age-related cataract. However, it is not known if these metals are present in a state that is permissive for redox reactions that may lead to the formation of free radicals. In addition, there is little data available concerning the concentration and lenticular distribution of ferritin, the major intracellular Fe-sequestering protein, in the lens. The aim of the present work was therefore to determine the distribution of ferritin and the redox-availability of Fe and Cu in healthy and cataractous lenses. Lens ferritin distribution was assessed by ELISA and immunohistochemistry. A modified ELISA detected ferritin in an 'insoluble' lens protein fraction. Ferritin levels were not significantly different in the cortex vs nucleus of healthy lenses. In contrast, ferritin levels in the cataractous lens nuclei appeared to be 70% lower compared to the cortex. This was at least partially due to the presence of ferritin within an insoluble protein fraction of the homogenized lenses. In normal lenses, ferritin staining was most intense in the epithelium, with diffuse staining observed throughout the cortex and nucleus. The redox-availability of lenticular metals was determined using: (1) autometallography; (2) Ferene-S as a chromogenic Fe chelator; and (3) NO release from nitrosocysteine to probe for redox-active Cu. The autometallography studies showed that the cataractous lenses stained more heavily for redox-active metals in both the nucleus and cortex when compared to age-matched control lenses. Chelatable Fe was detected in homogenized control lenses after incubation with Ferene-S, with almost three-fold higher levels detected in the cataractous lenses on average. The Cu-catalysed liberation of NO from added nitrosocysteine was not demonstrated in any lens sample. When exogenous Cu (50 n M) was added to the lenses, it was rapidly chelated. The cataractous samples were approximately twice as effective at redox-inactivation of added Cu. These studies provide evidence that a chelatable pool of potentially redox-active Fe is present at increased concentrations in human cataractous lenses. In contrast, it seems that lenticular Cu may not be readily available for participation in redox reactions.
以往研究表明,与年龄相关的白内障患者晶状体中铁和铜的含量会升高。然而,目前尚不清楚这些金属是否以一种能够促进可能导致自由基形成的氧化还原反应的状态存在。此外,关于晶状体中主要的细胞内铁螯合蛋白铁蛋白的浓度和晶状体分布,现有数据很少。因此,本研究的目的是确定健康晶状体和白内障晶状体中铁蛋白的分布以及铁和铜的氧化还原活性。通过酶联免疫吸附测定(ELISA)和免疫组织化学评估晶状体铁蛋白分布。一种改良的ELISA法检测到“不溶性”晶状体蛋白组分中的铁蛋白。健康晶状体皮质和核中的铁蛋白水平无显著差异。相比之下,白内障晶状体核中的铁蛋白水平似乎比皮质低70%。这至少部分是由于匀浆晶状体的不溶性蛋白组分中存在铁蛋白。在正常晶状体中,铁蛋白染色在上皮细胞中最为强烈,在整个皮质和核中均观察到弥漫性染色。使用以下方法测定晶状体金属的氧化还原活性:(1)自动金属显影术;(2)Ferene-S作为显色性铁螯合剂;(3)从亚硝基半胱氨酸释放一氧化氮以探测氧化还原活性铜。自动金属显影术研究表明,与年龄匹配的对照晶状体相比,白内障晶状体的核和皮质中氧化还原活性金属的染色更深。与Ferene-S孵育后,在匀浆对照晶状体中检测到可螯合铁,白内障晶状体中平均检测到的水平几乎高出三倍。在任何晶状体样品中均未证实添加的亚硝基半胱氨酸在铜催化下释放一氧化氮。当向晶状体中添加外源性铜(50 nM)时,它会迅速被螯合。白内障样品对添加铜的氧化还原失活作用约为对照样品的两倍。这些研究提供了证据,表明在人类白内障晶状体中,具有潜在氧化还原活性的可螯合铁池浓度升高。相比之下,晶状体中的铜似乎不易参与氧化还原反应。