期刊
HEART RHYTHM
卷 11, 期 6, 页码 1015-1023出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.hrthm.2014.02.021
关键词
Arrhythmia; Atrial fibrillation; Na(v)1.5; SCN5A; Sodium; PITX2; Polymorphism; SNP
资金
- Universite Pierre et Marie Curie
- INSERM
- Agence Nationale de la Recherche [ANR-09-GENO-003-CaR-NaC]
- French Ministry of Health [PHRC AOR04070, P040411]
- NIE [R01 HL094450]
BACKGROUND Mutations in the SCN5A gene, encoding the alpha subunit of the cardiac Na+ channel, Na(v)1.5, can result in several Life-threatening arrhythmias. OBJECTIVE To characterize a distal truncating SCN5A mutation, R1860Gfs*12, identified in a family with different phenotypes including sick sinus syndrome, atrial fibrillation (AF), atrial flutter, and atrioventricular block. METHODS Patch-clamp and biochemical analyses were performed in human embryonic kidney 293 cells transfected with wild-type (WT) and/or mutant channels. RESULTS The mutant channel expressed atone caused a 70% reduction in inward sodium current (I-Na) density compared to WT currents, which was consistent with its partial proteasomal degradation. It also Led to a negative shift of steady-state inactivation and to a persistent current. When mimicking the heterozygous state of the patients by coexpressing WT and R1860Gfs*12 channels, the biophysical properties of I-Na were still altered and the mutant channel a subunits still interacted with the WT channels. Since the proband developed paroxysmal AF at a young age, we screened 17 polymorphisms associated with AF risk in this family and showed that the proband carries at-risk polymorphisms upstream of PITX2, a gene widely associated with AF development. In addition, when mimicking the difference in resting membrane potentials between cardiac atria and ventricles in human embryonic kidney 293 cells or when using computer model simulations, R1860Gfs*12 induced a more drastic decrease in I-Na at the atrial potential. CONCLUSION We have identified a distal truncated SCN5A mutant associated with gain- and Loss-of-function effects, Leading to sick sinus syndrome and atrial arrhythmias. A constitutively higher susceptibility to arrhythmias of atrial tissues and genetic variability could explain the complex phenotype observed in this family.
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