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Corneal epithelial regeneration pathways" is not the name of a single molecule, receptor, enzyme, or druggable protein. Instead, it refers collectively to the complex network of cellular processes and molecular signaling cascades that govern the renewal and repair of the corneal epithelium. The primary drivers are limbal stem cells (LSCs), which reside at the corneoscleral junction ("limbus") and give rise to transient amplifying cells that proliferate and differentiate into mature corneal epithelial layers. Key regulatory signals include Wnt and Notch signaling for proliferation/differentiation balance; SPARC has been identified as an adaptive regeneration marker upregulated during wound healing. Disruption in these regenerative processes—such as from LSCD—leads to vision loss due to failure of normal surface maintenance. Current therapeutic strategies focus on transplantation/expansion of LSCs using various culture systems; modulation of key signaling networks is under investigation for improving outcomes. Because this entry describes broad biological processes rather than a discrete molecular entity, it should not be considered a canonical therapeutic target but rather an area encompassing multiple potential targets within its component molecules/pathways.
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