Role of HGF/c-Met in serum-starved ARPE-19 cells

Korean J Ophthalmol. 2007 Dec;21(4):244-50. doi: 10.3341/kjo.2007.21.4.244.

Abstract

Purpose: Hepatocyte growth factor (HGF) and its receptor (HGFR/c-Met) regulate motility, mitogenesis, and morphogenesis in a cell type-dependent fashion. We report the role of HGF and c-Met on stress-induced ARPE-19 human retinal pigment epithelial (RPE) cells in this study.

Methods: The cells were cultured either with or without serum. Southern and Western blot analyses were done to determine the expression patterns of HGF/c-Met in serum-starved ARPE-19 cells. The cell proliferation pattern in serum-starved condition was analyzed using MTS assay. Inhibition level of cell proliferation was analyzed using a neutralizing monoclonal antibody against c-Met (2 microg/ml).

Results: Abnormal cell proliferation and scattering of ARPE-19 cells was observed under serum starvation. HGF/c-Met were expressed in serum-starved ARPE-19 cells. ARPE-19 cell proliferation was also enhanced with recombinant HGF treatment. Neutralization against c-Met inhibited the proliferation of serum-deprived ARPE-19 by 64.5% (n=9, S.D. 5.5%). Serum starvation appears to induce epithelial-mesenchymal transition of ARPE-19 cells, resulting in scatter, and the expression of alpha-smooth muscle actin (alpha-SMA), a marker for fibrosis.

Conclusions: In conclusion, c-Met induced under non-physiologic conditions has significant effects on the activation of RPE cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Southern
  • Blotting, Western
  • Cell Movement / physiology
  • Cell Proliferation
  • Cells, Cultured
  • Culture Media, Serum-Free
  • Gene Expression*
  • Hepatocyte Growth Factor / biosynthesis
  • Hepatocyte Growth Factor / genetics*
  • Humans
  • Mitosis / physiology
  • Pigment Epithelium of Eye / cytology
  • Pigment Epithelium of Eye / metabolism*
  • Polymerase Chain Reaction
  • Proto-Oncogene Proteins c-met / biosynthesis
  • Proto-Oncogene Proteins c-met / genetics*
  • RNA / genetics*

Substances

  • Culture Media, Serum-Free
  • RNA
  • Hepatocyte Growth Factor
  • Proto-Oncogene Proteins c-met