The NADPH oxidase Nox4 has anti-atherosclerotic functions

Eur Heart J. 2015 Dec 21;36(48):3447-56. doi: 10.1093/eurheartj/ehv460. Epub 2015 Sep 17.


Aims: Oxidative stress is thought to be a risk for cardiovascular disease and NADPH oxidases of the Nox family are important producers of reactive oxygen species. Within the Nox family, the NADPH oxidase Nox4 has a unique position as it is constitutively active and produces H2O2 rather than [Formula: see text] . Nox4 is therefore incapable of scavenging NO and its low constitutive H2O2 production might even be beneficial. We hypothesized that Nox4 acts as an endogenous anti-atherosclerotic enzyme.

Methods and results: Tamoxifen-induced Nox4-knockout mice were crossed with ApoE⁻/⁻ mice and spontaneous atherosclerosis under regular chow as well as accelerated atherosclerosis in response to partial carotid artery ligation under high-fat diet were determined. Deletion of Nox4 resulted in increased atherosclerosis formation in both models. Mechanistically, pro-atherosclerotic and pro-inflammatory changes in gene expression were observed prior to plaque development. Moreover, inhibition of Nox4 or deletion of the enzyme in the endothelium but not in macrophages resulted in increased adhesion of macrophages to the endothelial surface.

Conclusions: The H2O2-producing NADPH oxidase Nox4 is an endogenous anti-atherosclerotic enzyme. Nox4 inhibitors, currently under clinical evaluation, should be carefully monitored for cardiovascular side-effects.

Keywords: ApoE; Arteriosclerosis; Inflammation; Lipids; NADPH oxidase; Reactive oxygen species; Remodelling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apolipoproteins E / metabolism
  • Atherosclerosis / physiopathology*
  • Carotid Arteries / metabolism
  • Cell Adhesion / physiology
  • Hydrogen Peroxide / metabolism
  • Leukocytes / physiology
  • Ligation
  • Mice
  • Mice, Knockout
  • Microarray Analysis
  • NADPH Oxidase 4
  • NADPH Oxidases / physiology*
  • Oxidative Stress / physiology
  • Reactive Oxygen Species / metabolism


  • Apolipoproteins E
  • Reactive Oxygen Species
  • Hydrogen Peroxide
  • NADPH Oxidase 4
  • NADPH Oxidases
  • Nox4 protein, mouse