Hepatocyte Growth Factor Suppresses Inflammation and Promotes Epithelium Repair in Corneal Injury

Mol Ther. 2017 Aug 2;25(8):1881-1888. doi: 10.1016/j.ymthe.2017.04.020. Epub 2017 May 11.

Abstract

Corneal injuries are among the major causes of ocular morbidity and vision impairment. Optimal epithelial wound healing is critical for the integrity and transparency of the cornea after injury. Hepatocyte growth factor (HGF) is a mitogen and motility factor that primarily regulates epithelial cell function. Herein, we investigate the effect of HGF on proliferation of corneal epithelial cells (CECs) in inflamed conditions both in vitro and in vivo. We demonstrate that HGF not only promotes CEC proliferation in homeostatic conditions but also reverses the anti-proliferative effect of the inflammatory environment on these cells. Furthermore, using a mouse model of ocular injury, we show that HGF treatment suppresses ocular inflammation and actively augments CEC proliferation, leading to improved and accelerated corneal epithelial repair. These findings have potential translational implications and could provide a framework for the development of novel HGF-based therapies for corneal epithelial defects.

Keywords: corneal epithelium; hepatocyte growth factor; injury and inflammation; wound repair.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Biomarkers
  • CD11b Antigen / metabolism
  • Cell Proliferation
  • Corneal Injuries / genetics*
  • Corneal Injuries / metabolism*
  • Corneal Injuries / pathology
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Models, Animal
  • Epithelial Cells / metabolism
  • Epithelium / metabolism*
  • Epithelium / pathology
  • Gene Expression
  • Hepatocyte Growth Factor / genetics*
  • Hepatocyte Growth Factor / metabolism
  • Humans
  • Inflammation / genetics
  • Inflammation / metabolism
  • Inflammation / therapy
  • Inflammation Mediators / metabolism
  • Mice
  • Wound Healing / genetics*

Substances

  • Biomarkers
  • CD11b Antigen
  • Cytokines
  • Inflammation Mediators
  • Hepatocyte Growth Factor