Excessive Corneal Endothelial Single Cell Loss Following Endothelial Injuries

Yuan-Kai Fu, Matthew Lin, Kuo-Hsuan Hung, Lung-Kun Yeh, HsinYuan Tan
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Abstract

Corneal endothelial dysfunction is the main cause for more than 50% of corneal transplantations. Human corneal endothelial cells are generally viewed as non-proliferative in vivo. Any injury that results in endothelial loss exceeding the critical threshold can cause irreversible endothelial functional decompensation, leading to corneal edema and vision loss. Currently, the mainstay treatment for irreversible corneal dysfunction is corneal transplantation. In this work, using well-established imaging technique of specular microscopy, we revisited the endothelial damage following three common corneal endothelial injury scenarios: post-cataract surgery, endothelial dystrophy, and corneal penetrating injury. We identified unexpected, stochastic single-cell loss in the corneal endothelium following primary injuries, persisting well beyond the expected wound healing period, a phenomenon that has not been previously highlighted. This finding offers a potential explanation for the chronic endothelial cell loss following a primary injury. Further investigation could provide valuable insights for improving clinical management strategies for corneal endothelial dysfunction.
角膜内皮损伤后角膜内皮单细胞丢失过多
角膜内皮功能障碍是 50%以上角膜移植手术的主要原因。人类角膜内皮细胞在体内一般被视为非增殖性细胞。任何导致内皮损失超过临界阈值的损伤都会引起不可逆的内皮功能失调,导致角膜水肿和视力丧失。目前,治疗不可逆角膜功能障碍的主要方法是角膜移植。在这项研究中,我们利用成熟的镜面显微成像技术,重新研究了三种常见角膜内皮损伤情况下的内皮损伤:白内障手术后、内皮营养不良和角膜穿透性损伤。我们发现原发性损伤后,角膜内皮会出现意想不到的随机单细胞损失,且持续时间远远超过预期的伤口愈合期,这是以前从未强调过的现象。这一发现为原发性损伤后内皮细胞的慢性丢失提供了潜在的解释。进一步的研究可为改进角膜内皮功能障碍的临床管理策略提供有价值的见解。
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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