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Coeal wounds usually heal quickly;but diabetic patients have more fragile coeas and experience delayed and painful healing.In the present study,we compared the healing capacity of coeal epithelial cells (CECs)between normal and diabetic conditions and the potential mechanisms.Primary murine CEC derived from wild-type and diabetic (db/db) mice,as well as primary human CEC were prepared.Human CEC were exposed to high glucose (30 mM) to mimic diabetic conditions.Cell migration and proliferation were assessed using Scratch test and MTT assays,respectively.Reactive oxygen species (ROS) production in the cells was measured using dichlorofluorescein reagent.Weste blot was used to evaluate the expression levels of Akt.Transepithelial electrical resistance (TEER) and zonula occludens-1 (ZO-1) expression were used to determine tight junction integrity.We found that the diabetic CEC displayed significantly slower cell proliferation and migration compared with the normal CEC from both mice and humans.Furthermore,ROS production was markedly increased in CEC grown under diabetic conditions.Treatment with an antioxidant N-acetyl cysteine (NAC,100 μM) significantly decreased ROS production and increased wound healing in diabetic CEC.Barrier function was significantly reduced in both diabetic mouse and human CEC,while NAC treatment mitigated these effects.We further showed that Akt signaling was impaired in diabetic CEC,which was partially improved by NAC treatment.These results show that diabetic conditions lead to delayed wound-healing capacity of CEC and impaired tight junction formation in both mice and human.Increased ROS production and inhibited Akt signaling may contribute to this outcome,implicating these as potential targets for treating coeal wounds in diabetic patients.