Hyperphosphorylation of the cardiac ryanodine receptor at serine 2808 is not involved in cardiac dysfunction after myocardial infarction

Circ Res. 2012 Mar 16;110(6):831-40. doi: 10.1161/CIRCRESAHA.111.255158. Epub 2012 Feb 2.

Abstract

Rationale: Abnormal behavior of the cardiac ryanodine receptor (RyR2) has been linked to cardiac arrhythmias and heart failure (HF) after myocardial infarction (MI). It has been proposed that protein kinase A (PKA) hyperphosphorylation of the RyR2 at a single residue, Ser-2808, is a critical mediator of RyR dysfunction, depressed cardiac performance, and HF after MI.

Objective: We used a mouse model (RyRS2808A) in which PKA hyperphosphorylation of the RyR2 at Ser-2808 is prevented to determine whether loss of PKA phosphorylation at this site averts post MI cardiac pump dysfunction.

Methods and results: MI was induced in wild-type (WT) and S2808A mice. Myocyte and cardiac function were compared in WT and S2808A animals before and after MI. The effects of the PKA activator Isoproterenol (Iso) on L-type Ca(2+) current (I(CaL)), contractions, and [Ca(2+)](I) transients were also measured. Both WT and S2808A mice had depressed pump function after MI, and there were no differences between groups. MI size was also identical in both groups. L type Ca(2+) current, contractions, Ca(2+) transients, and SR Ca(2+) load were also not significantly different in WT versus S2808A myocytes either before or after MI. Iso effects on Ca(2+) current, contraction, Ca(2+) transients, and SR Ca(2+) load were identical in WT and S2808A myocytes before and after MI at both low and high concentrations.

Conclusions: These results strongly support the idea that PKA phosphorylation of RyR-S2808 is irrelevant to the development of cardiac dysfunction after MI, at least in the mice used in this study.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Arrhythmias, Cardiac / genetics
  • Arrhythmias, Cardiac / metabolism*
  • Arrhythmias, Cardiac / mortality
  • Calcium / metabolism
  • Calcium Channels, L-Type / physiology
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Fibrosis / genetics
  • Fibrosis / metabolism
  • Heart Failure / genetics
  • Heart Failure / metabolism
  • Heart Failure / mortality
  • Mice
  • Mice, Mutant Strains
  • Myocardial Contraction / physiology
  • Myocardial Infarction / genetics*
  • Myocardial Infarction / metabolism*
  • Myocardial Infarction / mortality
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • Phenotype
  • Phosphorylation / physiology
  • Ryanodine Receptor Calcium Release Channel / genetics*
  • Ryanodine Receptor Calcium Release Channel / metabolism*
  • Sarcoplasmic Reticulum / metabolism
  • Serine / metabolism
  • Ventricular Remodeling / physiology

Substances

  • Calcium Channels, L-Type
  • Ryanodine Receptor Calcium Release Channel
  • Serine
  • Cyclic AMP-Dependent Protein Kinases
  • Calcium