DJ-1/park7 modulates vasorelaxation and blood pressure via epigenetic modification of endothelial nitric oxide synthase

Cardiovasc Res. 2014 Mar 1;101(3):473-81. doi: 10.1093/cvr/cvt274. Epub 2013 Dec 9.

Abstract

Aims: DJ-1/park7, a multifunctional protein, may play essential roles in the vascular system. However, the function of DJ-1/park7 in vascular contractility has remained unclear. The present study was designed to investigate whether the DJ-1/park7 is involved in the regulation of vascular contractility and systolic blood pressure (SBP).

Methods and results: Norepinephrine (NE) elevated contraction in endothelium-intact vessels in a dose-dependent manner, to a greater extent in DJ-1/park7 knockout (DJ-1/park7(-/-)) mice than in wild-type (DJ-1/park7(+/+)) mice. Acetylcholine inhibited NE-evoked contraction in endothelium-intact vessels, and this was markedly impaired in DJ-1/park7(-/-) mice compared with DJ-1/park7(+/+). Nitric oxide (NO) production (82.1 ± 2.8% of control) and endothelial NO synthase (eNOS) expression (61.7 ± 8.9%) were lower, but H2O2 production (126.4 ± 8.6%) was higher, in endothelial cells from DJ-1/park7(-/-) mice than in those from DJ-1/park7(+/+) controls; these effects were reversed by DJ-1/park7-overexpressing endothelial cells from DJ-1/park7(-/-) mice. Histone deacetylase (HDAC)-1 recruitment and H3 histone acetylation at the eNOS promoter were elevated and diminished, respectively, in DJ-1/park7(-/-) mice compared with DJ-1/park7(+/+) controls. Moreover, SBP was significantly elevated in DJ-1/park7(-/-) mice compared with DJ-1/park7(+/+) controls, but this elevation was inhibited in mice treated with valproic acid, an inhibitor of Class I HDACs including HDAC-1.

Conclusion: These results demonstrate that DJ-1/park7 protein may be implicated in the regulation of vascular contractility and blood pressure, probably by the impairment of NO production through H2O2-mediated epigenetic inhibition of eNOS expression.

Keywords: DJ-1/park7; Epigenetic modification; Vascular contractility; eNOS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure
  • Endothelium, Vascular / metabolism*
  • Epigenesis, Genetic / genetics
  • Epigenesis, Genetic / physiology*
  • Hydrogen Peroxide / metabolism
  • Male
  • Mice
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase Type III / genetics*
  • Nitric Oxide Synthase Type III / metabolism
  • Oncogene Proteins / genetics
  • Oncogene Proteins / metabolism*
  • Peroxiredoxins
  • Protein Deglycase DJ-1
  • Vasodilation* / genetics
  • Vasodilation* / physiology

Substances

  • Oncogene Proteins
  • Nitric Oxide
  • Hydrogen Peroxide
  • Peroxiredoxins
  • Nitric Oxide Synthase Type III
  • Nos3 protein, mouse
  • PARK7 protein, mouse
  • Protein Deglycase DJ-1