Role of Caspase-3 in acute light damage to retina of rats.

Xiao Wang, Shi-Xing Hu, Wei Li, Shao-Chun Lin
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Abstract

Objective: To investigate the role of Caspase-3 in retinal damage caused by light exposure in rats.

Methods: Light injury to retina was induced by persistent exposure to illumination (intensity: 30 000 +/- 50 lux) of operating microscope for 30 minutes in the right eyes of Sprague-Dawley rats. The pathological changes of retina were observed under optical and electron microscopies at different time points, which were 6 hours, 1, 3, 7, and 15 days after the light exposure. Apoptosis of retinal cells was analyzed by flow cytometry. The activity of Caspase-3 was evaluated by using the Caspase-3 assay kit. At the same time, the expression of Caspase-3 protease was determined with Western blot analysis.

Results: The examination results of optical and transmission electron microscopes showed that edema of inner and outer segments of the retina, especially the chondriosome inside the inner segment, became obvious 6 hours after the light exposure. The change was deteriorated along with the increasing time. The structures of the discoidal valve dissociated in the outer segment simultaneously. Disorderly arranged nuclei, karyopycnosis, and thinning in the outer nuclear layer were observed. The retinal pigment epithelium almost disappeared during the later stage. The staining results of Annexin-V combined with PI demonstrated that the proportion of apoptotic cells increased with time. The proportion between 7th day (82.7%) and 15th day (80.4%), however, showed no significant difference. Caspase-3 became remarkably active with the lapse of time, which increased from 0.02 at 6th hour to the peak of 9.8 at 7th day before it started to descend. The Western blot detected a expression of the active form of Caspase-3 at 7th day and 15th day.

Conclusion: Apoptosis of photoreceptor cells is markedly involved in the light damage and Caspase-3 protease may play an important role in the apoptotic process of the retina after light exposure in rats.

Caspase-3在大鼠视网膜急性光损伤中的作用。
目的:探讨Caspase-3在光致大鼠视网膜损伤中的作用。方法:在30 000 +/- 50勒克斯的操作显微镜下持续照射30分钟,对Sprague-Dawley大鼠右眼视网膜造成光损伤。分别在光照后6 h、1、3、7、15 d的不同时间点,在光学和电子显微镜下观察视网膜的病理变化。流式细胞术检测视网膜细胞凋亡情况。采用Caspase-3检测试剂盒检测Caspase-3活性。同时采用Western blot法检测Caspase-3蛋白酶的表达。结果:光学显微镜和透射电镜检查结果显示,光照6小时后,视网膜内外段水肿明显,尤其是内段线粒体水肿明显。这种变化随着时间的增加而恶化。盘状瓣外段结构同时游离。细胞核排列混乱,核厚缩,外核层变薄。视网膜色素上皮在晚期几乎消失。Annexin-V联合PI染色结果显示,凋亡细胞比例随时间增加而增加。第7天(82.7%)与第15天(80.4%)的比例无显著差异。随着时间的推移,Caspase-3活性显著增强,从第6小时的0.02升高到第7天的9.8,然后开始下降。Western blot检测在第7天和第15天Caspase-3活性形式的表达。结论:大鼠光损伤后视网膜感光细胞凋亡明显参与,Caspase-3蛋白酶可能在视网膜的凋亡过程中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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