The cKit Inhibitor, Masitinib, Prevents Diabetes-Induced Retinal Vascular Leakage

Invest Ophthalmol Vis Sci. 2016 Mar;57(3):1201-6. doi: 10.1167/iovs.15-18065.

Abstract

Purpose: Stem cell factor (SCF) has recently demonstrated activity as a novel endothelial permeability factor that contributes to the development of diabetes-induced hyperpermeable retinal vasculature. This study investigated the therapeutic potential of masitinib, a pharmacologic inhibitor of the SCF receptor cKit, for prevention of diabetes-induced breakdown of blood retinal barrier (BRB).

Methods: Permeability assays were performed with human retinal microvascular endothelial cells (HRMECs) and murine retinal vasculature. Localization of vascular endothelial (VE)-cadherin and activation of SCF signaling pathway was determined by immunofluorescence and Western blotting assays. Mice and rats with streptozotocin (STZ)-induced diabetes were used to investigate the role of cKit and masitinib in diabetes-induced retinal vascular hyperpermeability.

Results: Masitinib substantially blocked SCF-induced phosphorylation of cKit in HRMECs. In vitro and in vivo vascular permeability assays showed that masitinib significantly inhibited SCF-induced endothelial hyperpermeability and junctional loss of VE-cadherin. Streptozotocin-induced diabetes was induced in cKit-mutant mice with low cKit expression in their endothelial cells. Although diabetic wild-type mice exhibited enhanced retinal vascular leakage, diabetic cKit-mutant mice showed no increase in retinal vascular leakage or alteration in the distribution of VE-cadherin; this indicates the crucial role of cKit in diabetes-induced breakdown of BRB. Moreover, in vivo prevention experiments showed that an intravitreal injection of masitinib substantially inhibited the development of hyperpermeable retinal vasculature.

Conclusions: These results provide the first demonstration that cKit inhibitors, such as masitinib, might be promising therapeutics for prevention of diabetes-induced breakdown of the BRB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzamides
  • Blood-Retinal Barrier / drug effects
  • Blotting, Western
  • Capillary Permeability / drug effects*
  • Cells, Cultured
  • Diabetes Mellitus, Experimental*
  • Diabetic Retinopathy / complications*
  • Diabetic Retinopathy / drug therapy
  • Diabetic Retinopathy / metabolism
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology
  • Gene Expression Regulation / drug effects
  • Humans
  • Immunohistochemistry
  • Intravitreal Injections
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Piperidines
  • Protein Kinase Inhibitors / administration & dosage
  • Pyridines
  • RNA / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Retinal Diseases / etiology
  • Retinal Diseases / metabolism
  • Retinal Diseases / prevention & control*
  • Retinal Vessels / drug effects
  • Retinal Vessels / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / drug effects
  • Stem Cell Factor / biosynthesis
  • Stem Cell Factor / genetics
  • Thiazoles / administration & dosage*
  • Vascular Resistance / drug effects*

Substances

  • Benzamides
  • Piperidines
  • Protein Kinase Inhibitors
  • Pyridines
  • Stem Cell Factor
  • Thiazoles
  • RNA
  • masitinib