Arginase 2 deficiency prevents oxidative stress and limits hyperoxia-induced retinal vascular degeneration

PLoS One. 2014 Nov 6;9(11):e110604. doi: 10.1371/journal.pone.0110604. eCollection 2014.

Abstract

Background: Hyperoxia exposure of premature infants causes obliteration of the immature retinal microvessels, leading to a condition of proliferative vitreoretinal neovascularization termed retinopathy of prematurity (ROP). Previous work has demonstrated that the hyperoxia-induced vascular injury is mediated by dysfunction of endothelial nitric oxide synthase resulting in peroxynitrite formation. This study was undertaken to determine the involvement of the ureahydrolase enzyme arginase in this pathology.

Methods and findings: Studies were performed using hyperoxia-treated bovine retinal endothelial cells (BRE) and mice with oxygen-induced retinopathy (OIR) as experimental models of ROP. Treatment with the specific arginase inhibitor 2(S)-amino-6-boronohexanoic acid (ABH) prevented hyperoxia-induced apoptosis of BRE cells and reduced vaso-obliteration in the OIR model. Furthermore, deletion of the arginase 2 gene protected against hyperoxia-induced vaso-obliteration, enhanced physiological vascular repair, and reduced retinal neovascularization in the OIR model. Additional deletion of one copy of arginase 1 did not improve the vascular pathology. Analyses of peroxynitrite by quantitation of its biomarker nitrotyrosine, superoxide by dihydroethidium imaging and NO formation by diaminofluoroscein imaging showed that the protective actions of arginase 2 deletion were associated with blockade of superoxide and peroxynitrite formation and normalization of NOS activity.

Conclusions: Our data demonstrate the involvement of arginase activity and arginase 2 expression in hyperoxia-induced vascular injury. Arginase 2 deletion prevents hyperoxia-induced retinal vascular injury by preventing NOS uncoupling resulting in decreased reactive oxygen species formation and increased nitric oxide bioavailability.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis
  • Arginase / antagonists & inhibitors
  • Arginase / genetics*
  • Arginase / metabolism
  • Cattle
  • Disease Models, Animal
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Humans
  • Hyperoxia / complications*
  • Infant, Newborn
  • Mice
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type III / metabolism
  • Oxidative Stress / drug effects
  • Oxidative Stress / genetics*
  • Peroxynitrous Acid / metabolism
  • Reactive Oxygen Species / metabolism
  • Retina / drug effects
  • Retina / metabolism
  • Retina / pathology
  • Retinal Degeneration / etiology
  • Retinal Degeneration / genetics
  • Retinal Degeneration / pathology
  • Retinal Degeneration / prevention & control*
  • Retinal Neovascularization / etiology
  • Retinal Neovascularization / genetics
  • Retinal Neovascularization / pathology
  • Retinal Neovascularization / prevention & control*
  • Retinopathy of Prematurity / genetics
  • Retinopathy of Prematurity / pathology
  • Retinopathy of Prematurity / prevention & control*
  • Superoxides / metabolism

Substances

  • Reactive Oxygen Species
  • Superoxides
  • Peroxynitrous Acid
  • Nitric Oxide
  • Nitric Oxide Synthase Type III
  • Arg2 protein, mouse
  • Arginase