Zeb1 facilitates corneal epithelial wound healing by maintaining corneal epithelial cell viability and mobility

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作者
Yingnan Zhang
Khoi K. Do
Fuhua Wang
Xiaoqin Lu
John Y. Liu
Chi Li
Brian P. Ceresa
Lijun Zhang
Douglas C. Dean
Yongqing Liu
机构
[1] University of Louisville School of Medicine,Department of Medicine
[2] University of the Incarnate Word,The Rosenberg School of Optometry
[3] Eye Institute and Eye Hospital of Shangdong First Medical University,James Brown Cancer Center
[4] University of Louisville School of Medicine,Department of Pharmacology and Toxicology
[5] University of Louisville School of Medicine,Department of Ophthalmology, Third People’s Hospital of Dalian
[6] Dalian Medical University,Department of Ophthalmology and Visual Sciences
[7] University of Louisville School of Medicine,undefined
来源
Communications Biology | / 6卷
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摘要
The cornea is the outmost ocular tissue and plays an important role in protecting the eye from environmental insults. Corneal epithelial wounding provokes pain and fear and contributes to the most ocular trauma emergency assessments worldwide. ZEB1 is an essential transcription factor in development; but its roles in adult tissues are not clear. We identify Zeb1 is an intrinsic factor that facilitates corneal epithelial wound healing. In this study, we demonstrate that monoallelic deletion of Zeb1 significantly expedites corneal cell death and inhibits corneal epithelial EMT-related cell migration upon an epithelial debridement. We provide evidence that Zeb1-regulation of corneal epithelial wound healing is through the repression of genes required for Tnfa-induced epithelial cell death and the induction of genes beneficial for epithelial cell migration. We suggest utilizing TNF-α antagonists would reduce TNF/TNFR1-induced cell death in the corneal epithelium and inflammation in the corneal stroma to help corneal wound healing.
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