A C-terminal fragment BIGH3 protein with an RGDRGD motif inhibits corneal neovascularization in vitro and in vivo

Exp Eye Res. 2013 Jul:112:10-20. doi: 10.1016/j.exer.2013.03.014. Epub 2013 Apr 3.

Abstract

An Arg-Gly-Asp (RGD) motif in the fourth FAS1 domain of the human BIGH3 (transforming growth factor-β1-inducible gene-h3) protein has been reported to play an important role in mediating tumor angiogenesis. The aim of this study was to investigate the inhibitory effect of a modified C-terminal fragment BIGH3 protein with an RGDRGD motif on corneal neovascularization in vitro and in vivo. Recombinant C-terminal fragment BIGH3 protein with wild-type sequence and modified C-terminal fragment BIGH3 protein containing an RGDRGD motif were successfully expressed and purified. We demonstrated that both proteins significantly inhibited vascular endothelial growth factor (VEGF)-induced human umbilical vein endothelial cell (HUVEC) adhesion, migration, and tube formation and induced cell apoptosis but failed to inhibit HUVEC proliferation. We determined that the mechanism underlying this activity was an interaction between BIGH3 and αvβ3 integrin, which blocked the phosphorylation of PI3K/Akt and ERK signaling pathways. The inhibitory effects of wild-type and modified C-terminal fragment BIGH3 proteins on angiogenesis were confirmed by a rabbit corneal neovascularization assay. More importantly, we provided evidence that the modified C-terminal fragment BIGH3 protein with an RGDRGD motif inhibited angiogenic activity far more effectively than did wild-type C-terminal fragment BIGH3. Collectively, our data show that a C-terminal fragment BIGH3 protein containing an RGDRGD motif might be promising as an effective drug in treating corneal neovascularization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Angiogenesis Inhibitors / chemistry
  • Angiogenesis Inhibitors / genetics
  • Angiogenesis Inhibitors / pharmacology*
  • Animals
  • Apoptosis / drug effects
  • Blood Vessels / drug effects
  • Blotting, Western
  • Caspases / metabolism
  • Cell Adhesion / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Corneal Neovascularization / metabolism
  • Corneal Neovascularization / prevention & control*
  • Disease Models, Animal
  • Extracellular Matrix Proteins / chemistry
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / pharmacology*
  • Flow Cytometry
  • Human Umbilical Vein Endothelial Cells
  • Integrin alphaVbeta3 / metabolism
  • Mutagenesis, Site-Directed
  • Oligopeptides / chemistry
  • Oligopeptides / genetics
  • Oligopeptides / pharmacology*
  • Peptide Fragments / chemistry
  • Peptide Fragments / genetics
  • Peptide Fragments / pharmacology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation
  • Plasmids
  • Protein Folding
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rabbits
  • Transforming Growth Factor beta / chemistry
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / pharmacology*
  • Vascular Endothelial Growth Factor A / pharmacology

Substances

  • Angiogenesis Inhibitors
  • Extracellular Matrix Proteins
  • Integrin alphaVbeta3
  • Oligopeptides
  • Peptide Fragments
  • Transforming Growth Factor beta
  • Vascular Endothelial Growth Factor A
  • betaIG-H3 protein
  • arginyl-glycyl-aspartic acid
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • Caspases