Eph signaling is regulated by miRNA‐210: Implications for corneal epithelial repair. Issue 1 (1st December 2021)

• Record Type: Journal Article
• Authors: Kaplan, Nihal; Liu, Min; Wang, Junyi; Yang, Wending; Fiolek, Elaina; Peng, Han; Lavker, Robert M.
• Is Part Of: FASEB journal. Volume 36:Issue 1(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-12-01
• Subjects: corneal epithelium -- Eph/ephrin signaling -- F‐actin -- microRNAs -- migration -- wound repair; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.202101423R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: A distinct boundary exists between the progenitor cells in the basal limbal epithelium and the more differentiated corneal epithelial basal cells. We have shown that reciprocal expression patterns of EphA2 and Ephrin‐A1 are likely to contribute to normal limbal‐corneal epithelial compartmentalization as well as play a role in response to injury. How this signaling axis is regulated remains unclear. We have demonstrated that microRNAs (miRNAs) play critical roles in corneal epithelial wound healing and several miRNAs (e.g. miR‐210) have been predicted to target ephrins. Previous expression profiling experiments demonstrated that miR‐210 is prominently expressed in corneal epithelial cells. RNA‐seq data acquired from miR‐210‐depleted HCECs showed up‐regulation of genes involved in cellular migration. In addition, miR‐210 is decreased after corneal injury while EphA2 is increased. Moreover, antago‐210‐treated HCECs markedly enhanced wound closure in a scratch wound assay. Antago‐210 treatment resulted in increased EphA2 protein levels as well as pS897‐EphA2, the pro‐migratory form of EphA2. As expected, Ephrin‐A1 levels were reduced, while levels of a well‐known target of miR‐210, Ephrin‐A3, were increased by antago‐210 treatment. The increase in migration with antago‐210 could be inhibited by Ephrin‐A1 overexpression, Ephrin‐A1‐Fc treatment or siRNA depletion of EphA2. However, depletion of Ephrin‐A3 did not have effects on the antago‐210‐induced increase in migration. In addition, Ephrin‐A1 overexpression and siEphA2 dampened EGFR signaling, which is increased by antago‐210. Our data clearly demonstrate a link between miR‐210 and EphA2/Ephrin‐A1 signaling that regulates, in part, corneal epithelial migration. This interaction might potentially control the limbal‐corneal epithelial boundary.