Oxidized Ca(2+)/calmodulin-dependent protein kinase II triggers atrial fibrillation

Circulation. 2013 Oct 15;128(16):1748-57. doi: 10.1161/CIRCULATIONAHA.113.003313. Epub 2013 Sep 12.

Abstract

Background: Atrial fibrillation (AF) is a growing public health problem without adequate therapies. Angiotensin II and reactive oxygen species are validated risk factors for AF in patients, but the molecular pathways connecting reactive oxygen species and AF are unknown. The Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) has recently emerged as a reactive oxygen species-activated proarrhythmic signal, so we hypothesized that oxidized CaMKIIδ could contribute to AF.

Methods and results: We found that oxidized CaMKII was increased in atria from AF patients compared with patients in sinus rhythm and from mice infused with angiotensin II compared with mice infused with saline. Angiotensin II-treated mice had increased susceptibility to AF compared with saline-treated wild-type mice, establishing angiotensin II as a risk factor for AF in mice. Knock-in mice lacking critical oxidation sites in CaMKIIδ (MM-VV) and mice with myocardium-restricted transgenic overexpression of methionine sulfoxide reductase A, an enzyme that reduces oxidized CaMKII, were resistant to AF induction after angiotensin II infusion.

Conclusions: Our studies suggest that CaMKII is a molecular signal that couples increased reactive oxygen species with AF and that therapeutic strategies to decrease oxidized CaMKII may prevent or reduce AF.

Keywords: angiotensin II; arrhythmias, cardiac; atrial fibrillation; calcium-calmodulin-dependent protein kinase type II; reactive oxygen species.

Publication types

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

MeSH terms

  • Aged
  • Angiotensin II / metabolism
  • Angiotensin II / pharmacology
  • Animals
  • Atrial Fibrillation / etiology*
  • Atrial Fibrillation / metabolism*
  • Atrial Fibrillation / prevention & control
  • Calcium Signaling / physiology
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism*
  • Feedback, Physiological / drug effects
  • Feedback, Physiological / physiology
  • Female
  • Heart Conduction System / metabolism*
  • Humans
  • Male
  • Methionine Sulfoxide Reductases / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Middle Aged
  • NADPH Oxidases / genetics
  • NADPH Oxidases / metabolism
  • Oxidation-Reduction
  • Ryanodine Receptor Calcium Release Channel / metabolism

Substances

  • Ryanodine Receptor Calcium Release Channel
  • Angiotensin II
  • NADPH Oxidases
  • neutrophil cytosolic factor 1
  • Methionine Sulfoxide Reductases
  • methionine sulfoxide reductase
  • CAMK2D protein, human
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Camk2d protein, mouse