Ryanodine receptor phosphorylation by oxidized CaMKII contributes to the cardiotoxic effects of cardiac glycosides

Hsiang Ting Ho, Bin Liu, Jedidiah S. Snyder, Qing Lou, Elizabeth A. Brundage, Florencia Velez-Cortes, Honglan Wang, Mark T. Ziolo, Mark E. Anderson, Chandan K. Sen, Xander H.T. Wehrens, Vadim V. Fedorov, Brandon J. Biesiadecki, Thomas J. Hund, Sándor Györke

Research output: Contribution to journalArticlepeer-review

Abstract

AimsRecent studies suggest that proarrhythmic effects of cardiac glycosides (CGs) on cardiomyocyte Ca2+ handling involve generation of reactive oxygen species (ROS). However, the specific pathway(s) of ROS production and the subsequent downstream molecular events that mediate CG-dependent arrhythmogenesis remain to be defined.Methods and resultsWe examined the effects of digitoxin (DGT) on Ca2+ handling and ROS production in cardiomyocytes using a combination of pharmacological approaches and genetic mouse models. Myocytes isolated from mice deficient in NADPH oxidase type 2 (NOX2KO) and mice transgenically overexpressing mitochondrial superoxide dismutase displayed markedly increased tolerance to the proarrhythmic action of DGT as manifested by the inhibition of DGT-dependent ROS and spontaneous Ca 2+ waves (SCW). Additionally, DGT-induced mitochondrial membrane potential depolarization was abolished in NOX2KO cells. DGT-dependent ROS was suppressed by the inhibition of PI3K, PKC, and the mitochondrial KATP channel, suggesting roles for these proteins, respectively, in activation of NOX2 and in mitochondrial ROS generation. Western blot analysis revealed increased levels of oxidized CaMKII in WT but not in NOX2KO hearts treated with DGT. The DGT-induced increase in SCW frequency was abolished in myocytes isolated from mice in which the Ser 2814 CaMKII phosphorylation site on RyR2 is constitutively inactivated.ConclusionThese results suggest that the arrhythmogenic adverse effects of CGs on Ca2+ handling involve PI3K-and PKC-mediated stimulation of NOX2 and subsequent NOX2-dependent ROS release from the mitochondria; mitochondria-derived ROS then activate CaMKII with consequent phosphorylation of RyR2 at Ser 2814.

Original languageEnglish (US)
Pages (from-to)165-174
Number of pages10
JournalCardiovascular research
Volume101
Issue number1
DOIs
StatePublished - Jan 1 2014
Externally publishedYes

Keywords

  • CaMKII
  • Calcium
  • Mitochondria
  • NADPH oxidase
  • Reactive oxygen species

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

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