期刊
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY
卷 2, 期 5, 页码 540-547出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCEP.109.872309
关键词
K-channel; arrhythmia (mechanisms); long QT syndrome; Andersen-Tawil syndrome; catecholaminergic polymorphic ventricular tachycardia
资金
- University of Wisconsin Cellular and Molecular Arrhythmia Research Program
- Mayo Clinic Windland Smith Rice Comprehensive Sudden Cardiac Death Research program
- National Heart, Lung, and Blood Institute [T32 HL07936]
- Graduate School of the University of Wisconsin
Background-KCNJ2 encodes Kir2.1, a pore-forming subunit of the cardiac inward rectifier current, I-K1. KCNJ2 mutations are associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia. The aim of this study was to characterize the biophysical and cellular phenotype of a KCNJ2 missense mutation, V227F, found in a patient with catecholaminergic polymorphic ventricular tachycardia. Methods and Results-Kir2.1-wild-type (WT) and V227F channels were expressed individually and together in Cos-1 cells to measure I-K1 by voltage clamp. Unlike typical Andersen-Tawil syndrome-associated KCNJ2 mutations, which show dominant negative loss of function, Kir2.1WT+V227F coexpression yielded I-K1 indistinguishable from Kir2.1-WT under basal conditions. To simulate catecholamine activity, a protein kinase A (PKA)-stimulating cocktail composed of forskolin and 3-isobutyl-1-methylxanthine was used to increase PKA activity. This PKA-simulated catecholaminergic stimulation caused marked reduction of outward I-K1 compared with Kir2.1-WT. PKA-induced reduction in I-K1 was eliminated by mutating the phosphorylation site at serine 425 (S425N). Conclusions-Heteromeric Kir2.1-V227F and WT channels showed an unusual latent loss of function biophysical phenotype that depended on PKA-dependent Kir2.1 phosphorylation. This biophysical phenotype, distinct from typical Andersen-Tawil syndrome mutations, suggests a specific mechanism for PKA-dependent I-K1 dysfunction for this KCNJ2 mutation, which correlates with adrenergic conditions underlying the clinical arrhythmia. (Circ Arrhythmia Electrophysiol. 2009; 2: 540-547.)
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