Regional Institute of Ophthalmology, Egmore, Chennai, Tamilnadu, India.
The Light Eye Hospital, Salem Main Rd, Dharmapuri, Tamil Nadu, 636701, India.
Biotechnol Lett. 2021 Jun;43(6):1241-1251. doi: 10.1007/s10529-021-03116-y. Epub 2021 Mar 25.
McCarey-Kaufman's (MK) medium and Optisol-GS medium are the most commonly employed media for human donor corneal preservation. In this study, we evaluated the preservation efficacy of discarded human donor corneas using a Thermo-reversible gelation polymer (TGP) added to these two media.
Thirteen human corneal buttons collected from deceased donors, which were otherwise discarded due to low endothelial cell density (ECD) were used. They were stored in four groups: MK medium, MK medium with TGP, Optisol-GS and Optisol-GS with TGP at 4 °C for 96 h. Slit lamp examination and specular microscopy were performed. Corneal limbal tissues from these corneas were then cultured using explant methodology one with and the other without TGP scaffold, for 21 days.
MK + TGP and Optisol-GS + TGP preserved corneas better than without TGP, which was observed by maintenance of ECD which was significantly higher in Optisol-GS + TGP than MK + TGP (p-value = 0.000478) and corneal thickness remaining the same for 96 h. Viable corneal epithelial cells could be grown from the corneas stored only in MK + TGP and Optisol-GS + TGP. During culture, the TGP scaffold helped maintain the native epithelial phenotype and progenitor/stem cell growth was confirmed by RT-PCR characterization.
TGP reconstituted with MK and Optisol-GS media yields better preservation of human corneal buttons in terms of relatively higher ECD maintenance and better in vitro culture outcome of corneal limbal tissue. This method has the potential to become a standard donor corneal transportation-preservation methodology and it can also be extended to other tissue or organ transportation upon further validation.
麦卡利-考夫曼(MK)培养基和 Optisol-GS 培养基是最常用于人类供体角膜保存的培养基。在这项研究中,我们评估了在这两种培养基中添加热可逆凝胶聚合物(TGP)对废弃人类供体角膜的保存效果。
使用从已故供体收集的 13 个角膜纽扣,由于内皮细胞密度(ECD)低而被丢弃。将它们分别储存在四个组中:MK 培养基、MK 培养基中添加 TGP、Optisol-GS 和 Optisol-GS 中添加 TGP,在 4°C 下保存 96 小时。进行裂隙灯检查和共焦显微镜检查。然后,使用组织外植体方法,在一个组中培养这些角膜的角膜缘组织,另一个组中不添加 TGP 支架,培养 21 天。
MK+TGP 和 Optisol-GS+TGP 比没有 TGP 更好地保存角膜,这可以通过维持 ECD 观察到,Optisol-GS+TGP 中的 ECD 明显高于 MK+TGP(p 值=0.000478),并且角膜厚度在 96 小时内保持不变。仅在 MK+TGP 和 Optisol-GS+TGP 中储存的角膜可以生长出有活力的角膜上皮细胞。在培养过程中,TGP 支架有助于维持天然上皮表型,通过 RT-PCR 特征证实了祖细胞/干细胞的生长。
TGP 与 MK 和 Optisol-GS 培养基重构可在相对较高的 ECD 维持和更好的角膜缘组织体外培养结果方面更好地保存人类角膜纽扣。这种方法有可能成为一种标准的供体角膜运输保存方法,并且可以在进一步验证后扩展到其他组织或器官的运输。