Nitric Oxide Increases Cardiac IK1 by Nitrosylation of Cysteine 76 of Kir2.1 Channels

• Published in: Circulation research 2009-08, Vol.105 (4), p.383-392
• Main Authors: Gómez, Ricardo, Caballero, Ricardo, Barana, Adriana, Amorós, Irene, Calvo, Enrique, López, Juan Antonio, Klein, Helene, Vaquero, Miguel, Osuna, Lourdes, Atienza, Felipe, Almendral, Jesús, Pinto, Ángel, Tamargo, Juan, Delpón, Eva
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; CHO Cells; Cricetinae; Cricetulus; Cysteine - genetics; Cysteine - metabolism; Endothelium-Dependent Relaxing Factors - metabolism; Endothelium-Dependent Relaxing Factors - pharmacology; Female; Fundamental and applied biological sciences. Psychology; Heart Atria - cytology; Heart Atria - metabolism; Humans; Intermediate-Conductance Calcium-Activated Potassium Channels - genetics; Intermediate-Conductance Calcium-Activated Potassium Channels - metabolism; Male; Membrane Potentials - drug effects; Membrane Potentials - physiology; Mutagenesis, Site-Directed; Myocytes, Cardiac - cytology; Myocytes, Cardiac - metabolism; Nitric Oxide - metabolism; Nitric Oxide - pharmacology; Oxidation-Reduction - drug effects; Potassium Channels, Inwardly Rectifying - genetics; Potassium Channels, Inwardly Rectifying - metabolism; Vertebrates: cardiovascular system
• ISSN: 0009-7330; 1524-4571
• DOI: 10.1161/CIRCRESAHA.109.197558

RATIONALE:The cardiac inwardly rectifying K current (IK1) plays a critical role in modulating excitability by setting the resting membrane potential and shaping phase 3 of the cardiac action potential. OBJECTIVE:This study aims to analyze the effects of nitric oxide (NO) on human atrial IK1 and on Kir2.1 channels, the major isoform of inwardly rectifying channels present in the human heart. METHODS AND RESULTS:Currents were recorded in enzymatically isolated myocytes and in transiently transfected CHO cells, respectively. NO at myocardial physiological concentrations (25 to 500 nmol/L) increased inward and outward IK1 and IKir2.1. These effects were accompanied by hyperpolarization of the resting membrane potential and a shortening of the duration of phase 3 of the human atrial action potential. The IKir2.1 increase was attributable to an increase in the open probability of the channel. Site-directed mutagenesis analysis demonstrated that NO effects were mediated by the selective S-nitrosylation of Kir2.1 Cys76 residue. Single ion monitoring experiments performed by liquid chromatography/tandem mass spectrometry suggested that the primary sequence that surrounds Cys76 determines its selective S-nitrosylation. Chronic atrial fibrillation, which produces a decrease in NO bioavailability, decreased the S-nitrosylation of Kir2.1 channels in human atrial samples as demonstrated by a biotin-switch assay, followed by Western blot. CONCLUSIONS:The results demonstrated that, under physiological conditions, NO regulates human cardiac IK1 through a redox-related process.