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DOI: 10.3791/67326-v
Porcine corneal ex vivo organ culture and epithelial wound healing provide an economical, ethical, reproducible, and quantitative means for testing the ocular toxicity of chemicals. They also aid in elucidating mechanisms underlying the regulation of epithelialization and tissue repair, and in evaluating therapeutics for treating diabetic keratopathy and delayed wound healing.
We are investigating cornea innate immunity in diabetic wound healing. Specifically, we aim to understand why diabetic patients are more susceptible to bacterial infection and what causes delayed wound healing associated with hyperglycemia. We identified that the balance between IL-1 beta and IL-1 receptor antagonist, as well as TGF beta one and TGF beta three, is important for corneal wound healing.
This could lead to new treatment for diabetic keratopathy. Our model mimic human delayed wound healing in diabetic patients. This allows us to study programmed cell death pathway and develop targeted therapies.
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