Jamie S Rush1, Michael A Boeving2, William L Berry2, Brian P Ceresa3. 1. Department of Pharmacology and Toxicology, University of Louisville, Louisville, Kentucky, United States. 2. Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma, United States. 3. Department of Pharmacology and Toxicology, University of Louisville, Louisville, Kentucky, United States Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma, United States.
Abstract
PURPOSE: In many cell types, the E3 ubiquitin ligase, c-Cbl, induces ligand-dependent ubiquitylation of the epidermal growth factor receptor (EGFR) and targets the receptor for lysosomal degradation. The goal of this study was to determine whether c-Cbl is a negative regulator of EGFR in the corneal epithelium and if it can be inhibited to promote corneal epithelial homeostasis. METHODS: Expression and activity of c-Cbl were blocked in immortalized human corneal epithelial cells (hTCEpi) using RNAi and pharmacological agents ([4-amino-5-(4-methylphenyl)-7-(t-butyl)pyrazolo-d-3,4-pyrimidine] or PP1). Following c-Cbl inhibition, cells were assessed for ligand-dependent receptor ubiquitylation, receptor phosphorylation, and in vitro wound healing. Subsequent experiments used PP1 in hTCEpi cells and monitored in vivo murine corneal epithelial wound healing. RESULTS: Knockdown and inhibition of c-Cbl decreased ligand-dependent ubiquitylation of the EGFR and prolonged receptor activity as measured by tyrosine phosphorylation. Further, these treatments also increased the extent of ligand-dependent corneal epithelial wound healing in vitro and in vivo. CONCLUSION: Manipulating the duration of EGFR activity can enhance the rate of restoration of the corneal epithelial layer. Based on our findings, c-Cbl is a new therapeutic target to enhance EGFR-mediated corneal epithelial homeostasis that bypasses the limitations of previous approaches. Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.
PURPOSE: In many cell types, the E3 ubiquitin ligase, c-Cbl, induces ligand-dependent ubiquitylation of the epidermal growth factor receptor (EGFR) and targets the receptor for lysosomal degradation. The goal of this study was to determine whether c-Cbl is a negative regulator of EGFR in the corneal epithelium and if it can be inhibited to promote corneal epithelial homeostasis. METHODS: Expression and activity of c-Cbl were blocked in immortalized human corneal epithelial cells (hTCEpi) using RNAi and pharmacological agents ([4-amino-5-(4-methylphenyl)-7-(t-butyl)pyrazolo-d-3,4-pyrimidine] or PP1). Following c-Cbl inhibition, cells were assessed for ligand-dependent receptor ubiquitylation, receptor phosphorylation, and in vitro wound healing. Subsequent experiments used PP1 in hTCEpi cells and monitored in vivo murine corneal epithelial wound healing. RESULTS: Knockdown and inhibition of c-Cbl decreased ligand-dependent ubiquitylation of the EGFR and prolonged receptor activity as measured by tyrosine phosphorylation. Further, these treatments also increased the extent of ligand-dependent corneal epithelial wound healing in vitro and in vivo. CONCLUSION: Manipulating the duration of EGFR activity can enhance the rate of restoration of the corneal epithelial layer. Based on our findings, c-Cbl is a new therapeutic target to enhance EGFR-mediated corneal epithelial homeostasis that bypasses the limitations of previous approaches. Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.
Authors: C Kenneth Kassenbrock; Seija Hunter; Pamela Garl; Gary L Johnson; Steven M Anderson Journal: J Biol Chem Date: 2002-05-06 Impact factor: 5.157
Authors: Jamie S Rush; David P Bingaman; Paul G Chaney; Martin B Wax; Brian P Ceresa Journal: Invest Ophthalmol Vis Sci Date: 2016-11-01 Impact factor: 4.799