Akeo Kiyoshi, Hiramitsu Tadahisa, Yorifuji Hiroshi, Okisaka Shigekuni
Department of Ophthalmology, Takasaki National Hospital, Takasaki-shi, Gunma, Japan.
Pigment Cell Res. 2002 Oct;15(5):341-7. doi: 10.1034/j.1600-0749.2002.02054.x.
The ferrous ions released from haemoglobin and storage-transferrin ions cause oxidative stress in the eyes. We observed the phagocytotic process of the photoreceptor outer segment discs peroxidized by ferrous ions in the retinal pigment epithelial (RPE) cells in vitro, and investigated how the ferrous ions influenced RPE in vitro and the photoreceptor outer segment discs. We obtained isolated photoreceptor outer segment discs using sucrose gradient of specific gravity after homogenizing porcine retinas. After bovine RPE cells were cultured with isolated photoreceptor outer segment discs containing FeCl2 for 5 and 24 h, we incubated the specimens with rhodamine phalloidin, antimouse alpha-tubulin antibody and antimouse Ig G (FITC and rhodamine labelled). We observed the specimens by a laser scanning microscopy, and made the ultrathin sections with or without 2% uranyl acetate and 2% lead acetate for examination by transmission electron microscopy. Actin filaments and microtubules of specialized cells such as RPE cells were actively involved in phagocytosis of the photoreceptor outer segment discs. Microtubules were damaged during the phagocytotic process of the photoreceptor outer segment discs peroxidized by ferrous ions. The peroxidation increased the granular and aggregated autofluorescence of the photoreceptor outer segment discs. The membranes of the disc and the phagosomes, and lysosomes in RPE cells were damaged by ferrous ions and had fine particles with high electron density staining without uranium acetate and lead citrate. The cytoskeletons such as actin filaments and microtubules, and the membranes of the phagosomes and the lysosomes in RPE cells in vitro were damaged during the phagocytotic process of the photoreceptor outer segment discs peroxidized by ferrous ions.
血红蛋白和储存转铁蛋白离子释放的亚铁离子会在眼睛中引发氧化应激。我们在体外观察了视网膜色素上皮(RPE)细胞中被亚铁离子过氧化的光感受器外节盘的吞噬过程,并研究了亚铁离子如何在体外影响RPE和光感受器外节盘。我们通过对猪视网膜进行匀浆后使用特定比重的蔗糖梯度获得了分离的光感受器外节盘。在用含有FeCl2的分离光感受器外节盘培养牛RPE细胞5小时和24小时后,我们用罗丹明鬼笔环肽、抗小鼠α-微管蛋白抗体和抗小鼠Ig G(FITC和罗丹明标记)孵育标本。我们通过激光扫描显微镜观察标本,并制作有或没有2%醋酸铀和2%醋酸铅的超薄切片,用于透射电子显微镜检查。RPE细胞等特化细胞的肌动蛋白丝和微管积极参与光感受器外节盘的吞噬作用。在被亚铁离子过氧化的光感受器外节盘的吞噬过程中,微管受到损伤。过氧化增加了光感受器外节盘的颗粒状和聚集性自发荧光。光感受器外节盘以及RPE细胞中的吞噬体和溶酶体的膜被亚铁离子损伤,在没有醋酸铀和柠檬酸铅的情况下有高电子密度染色的细颗粒。在体外,被亚铁离子过氧化的光感受器外节盘的吞噬过程中,RPE细胞中的肌动蛋白丝和微管等细胞骨架以及吞噬体和溶酶体的膜受到损伤。