Constitutive overexpression of phosphomimetic phospholemman S68E mutant results in arrhythmias, early mortality, and heart failure: potential involvement of Na+/Ca2+ exchanger.

Abstract

Expression and activity of cardiac Na(+)/Ca(2+) exchanger (NCX1) are altered in many disease states. We engineered mice in which the phosphomimetic phospholemman S68E mutant (inhibits NCX1 but not Na(+)-K(+)-ATPase) was constitutively overexpressed in a cardiac-specific manner (conS68E). At 4-6 wk, conS68E mice exhibited severe bradycardia, ventricular arrhythmias, increased left ventricular (LV) mass, decreased cardiac output (CO), and ∼50% mortality compared with wild-type (WT) littermates. Protein levels of NCX1, calsequestrin, ryanodine receptor, and α(1)- and α(2)-subunits of Na(+)-K(+)-ATPase were similar, but sarco(endo)plasmic reticulum Ca(2+)-ATPase was lower, whereas L-type Ca(2+) channels were higher in conS68E hearts. Resting membrane potential and action potential amplitude were similar, but action potential duration was dramatically prolonged in conS68E myocytes. Diastolic intracellular Ca(2+) ([Ca(2+)](i)) was higher, [Ca(2+)](i) transient and maximal contraction amplitudes were lower, and half-time of [Ca(2+)](i) transient decline was longer in conS68E myocytes. Intracellular Na(+) reached maximum within 3 min after isoproterenol addition, followed by decline in WT but not in conS68E myocytes. Na(+)/Ca(2+) exchange, L-type Ca(2+), Na(+)-K(+)-ATPase, and depolarization-activated K(+) currents were decreased in conS68E myocytes. At 22 wk, bradycardia and increased LV mass persisted in conS68E survivors. Despite comparable baseline CO, conS68E survivors at 22 wk exhibited decreased chronotropic, inotropic, and lusitropic responses to isoproterenol. We conclude that constitutive overexpression of S68E mutant was detrimental, both in terms of depressed cardiac function and increased arrhythmogenesis.

• Authors: Jianliang Song, Erhe Gao, Jufang Wang, Xue-Qian Zhang, Tung O Chan, Walter J Koch, Xiying Shang, Jeffrey I Joseph, Blaise Z Peterson, Arthur M Feldman, Joseph Y Cheung
• Journal: American journal of physiology. Heart and circulatory physiology (Am J Physiol Heart Circ Physiol) Vol. 302 Issue 3 Pg. H770-81 (Feb 01 2012) ISSN: 1522-1539 [Electronic] United States
• PMID: 22081699 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Calcium Channels, L-Type
• Membrane Proteins
• NCX1 protein, mouse
• Phosphoproteins
• Receptors, Adrenergic, beta
• Sodium-Calcium Exchanger
• phospholemman
• Sodium
• Potassium
• Calcium

Topics

• Action Potentials (genetics, physiology)
• Animals
• Arrhythmias, Cardiac (genetics, metabolism, physiopathology)
• Bradycardia (genetics, metabolism, mortality)
• Calcium (metabolism)
• Calcium Channels, L-Type (physiology)
• Female
• Gene Expression (physiology)
• Heart Failure (genetics, metabolism, mortality)
• Male
• Membrane Proteins (genetics, metabolism)
• Mice
• Mice, Inbred Strains
• Mice, Transgenic
• Myocardial Contraction (physiology)
• Myocytes, Cardiac (cytology, physiology)
• Phosphoproteins (genetics, metabolism)
• Potassium (metabolism)
• Receptors, Adrenergic, beta (metabolism)
• Sodium (metabolism)
• Sodium-Calcium Exchanger (genetics, metabolism)