Abnormalities in intracellular Ca2+ regulation contribute to the pathomechanism of Tako-Tsubo cardiomyopathy

Eur Heart J. 2009 Sep;30(17):2155-64. doi: 10.1093/eurheartj/ehp240. Epub 2009 Jun 13.

Abstract

Aims: The Tako-Tsubo cardiomyopathy (TTC) is characterized by a transient contractile dysfunction that has been assigned to excessive catecholamine levels after episodes of severe emotional or physical stress. Several studies have indicated that beta-adrenoceptor stimulation is associated with alteration in gene expression of Ca(2+)-regulatory proteins. Thus, the present study investigated the gene expression of crucial proteins [sarcoplasmic Ca(2+) ATPase (SERCA2a), sarcolipin (SLN), phospholamban (PLN), ryanodine receptor (RyR2), and sodium-calcium exchanger (NCX)] involved in the Ca(2+)-regulating system in TTC.

Methods and results: In 10 consecutive patients, TTC was diagnosed by coronary angiography, ventriculography, and echocardiography. Endomyocardial biopsies were taken during the phase of severely impaired left ventricular (LV) function and after functional recovery. Non-diseased LV tissue from three donor hearts not used for transplantation served as healthy controls. Expression levels of Ca(2+)-regulatory proteins were analysed by means of real-time PCR, western blot, and immunohistochemistry. SLN, predominantly expressed in the atrial component, showed a remarkable ventricular expression in TTC patients. Gene expression of SERCA2a was significantly down-regulated. Conversely, PLN/SERCA2a ratio was increased. For PLN, dephosphorylation was documented using western blot and immunostaining of PLN-Ser(16) and PLN-Thr(17). No changes could be documented for NCX and RyR2.

Conclusion: In TTC, ventricular expression of SLN and dephosphorylation of PLN potentially result in a reduced SERCA2a activity and its Ca(2+) affinity. Thus, the TTC is associated with specific alteration of Ca(2+)-handling proteins, which might be crucial for contractile dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Calcium-Binding Proteins / metabolism*
  • Case-Control Studies
  • Female
  • Heart Ventricles / metabolism
  • Humans
  • Magnetic Resonance Angiography
  • Male
  • Middle Aged
  • Muscle Proteins / metabolism*
  • Phosphorylation
  • Protein Phosphatase 1 / metabolism
  • Proteolipids / metabolism*
  • Ryanodine Receptor Calcium Release Channel / metabolism*
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism*
  • Sodium-Calcium Exchanger / metabolism*
  • Takotsubo Cardiomyopathy / etiology*
  • Takotsubo Cardiomyopathy / metabolism

Substances

  • Calcium-Binding Proteins
  • Muscle Proteins
  • Proteolipids
  • Ryanodine Receptor Calcium Release Channel
  • Sodium-Calcium Exchanger
  • phospholamban
  • sarcolipin
  • Protein Phosphatase 1
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases