Department of Immunology and Stem Cell Biology, Aravind Medical Research Foundation, Madurai, Tamil Nadu, India.
Department of Cornea and Refractive Surgery, Aravind Eye Hospital and Post Graduate Institute of Ophthalmology, Madurai, Tamil Nadu, India.
Indian J Ophthalmol. 2019 Oct;67(10):1579-1584. doi: 10.4103/ijo.IJO_2026_18.
To compare the structural integrity and functional status of the donor corneas stored in Cornisol and Optisol-GS.
Fifteen optical grade corneal donor buttons (6 pairs; 3 individual) obtained from Rotary Aravind International Eye Bank were used for the study. The left eye of the paired sample was preserved in Cornisol and the right in Optisol-GS. The three individual buttons were used for the baseline data. The corneas were assessed with slit lamp and specular microscope before and after storage time (7, 10, or 14 days). They were then immunostained for markers of structural integrity (ZO-1, Phalloidin) and functionality (Na/K ATPase). The images were acquired using confocal microscope and analyzed using ImageJ software.
There was no difference in the clinical evaluation of the corneal layers between the two media. No marked variation was observed in the immunostaining data with reference to the storage period. Intact cellular integrity was identified in 91% (51%, 98%) [Median (min, max)] of cells in Cornisol and 94% (38%, 98%) cells in Optisol based on ZO-1 staining, comparable to the baseline data [87% (76%, 97%)]. Stress fibers were detected in 42.5% (1%, 88%) cells in Cornisol stored corneas and in 55% (11%, 94%) in Optisol when stained for actin cytoskeleton, which correlated with the presence of epithelial defect before storage and vacuolated endothelial cells after storage. No difference was observed between the two media based on the staining pattern for Na/K ATPase.
Cornisol and Optisol-GS are equivalent in maintaining the structural integrity and functionality of the donor corneas.
比较 Cornisol 和 Optisol-GS 保存的供体角膜的结构完整性和功能状态。
本研究使用了来自 Rotary Aravind 国际眼库的 15 个光学级角膜供体纽扣(6 对;3 个个体)。配对样本的左眼保存在 Cornisol 中,右眼保存在 Optisol-GS 中。三个个体纽扣用于基线数据。在储存时间(7、10 或 14 天)前后,使用裂隙灯和共聚焦显微镜评估角膜。然后,用标记结构完整性(ZO-1、鬼笔环肽)和功能(Na/K ATPase)的抗体对角膜进行免疫染色。使用共聚焦显微镜获取图像,并使用 ImageJ 软件进行分析。
两种培养基之间角膜各层的临床评估无差异。参照储存期,免疫染色数据无明显变化。用 ZO-1 染色,Cornisol 中 91%(51%,98%)[中位数(最小,最大)]的细胞和 Optisol 中 94%(38%,98%)的细胞具有完整的细胞完整性,与基线数据(87%(76%,97%))相当。在 Cornisol 储存的角膜中,用肌动蛋白细胞骨架染色检测到 42.5%(1%,88%)的细胞存在应激纤维,在 Optisol 中则为 55%(11%,94%),这与储存前上皮缺陷和储存后内皮细胞空泡化有关。基于 Na/K ATPase 的染色模式,两种培养基之间没有差异。
Cornisol 和 Optisol-GS 在维持供体角膜的结构完整性和功能方面等效。