Journal article
A sodium channel pore mutation causing Brugada syndrome
Heart rhythm, Vol.4(1), pp.46-53
2007
DOI: 10.1016/j.hrthm.2006.09.031
PMCID: PMC1779366
PMID: 17198989
Abstract
Brugada and long QT type 3 syndromes are linked to sodium channel mutations and clinically cause arrhythmias that lead to sudden death. We have identified a novel threonine-to-isoleucine missense mutation at position 353 (T353I) adjacent to the pore-lining region of domain I of the cardiac sodium channel (SCN5A) in a family with Brugada syndrome. Both male and female carriers are symptomatic at young ages, have typical Brugada-type electrocardiogram changes, and have relatively normal corrected QT intervals.
To characterize the properties of the newly identified cardiac sodium channel (SCN5A) mutation at the cellular level.
Using whole-cell voltage clamp, we found that heterologous expression of SCN5A containing the T353I mutation resulted in 74% ± 6% less peak macroscopic sodium current when compared with wild-type channels. A construct of the T353I mutant channel fused with green fluorescent protein failed to traffic properly to the sarcolemma, with a large proportion of channels sequestered intracellularly. Overnight exposure to 0.1 mM mexiletine, a Na
+ channel blocking agent, increased T353I channel trafficking to the membrane to near normal levels, but the mutant channels showed a significant late current that was 1.6% ± 0.2% of peak sodium current at 200 ms, a finding seen with long QT mutations.
The clinical presentation of patients carrying the T353I mutation is that of Brugada syndrome and could be explained by a cardiac Na
+ channel trafficking defect. However, when the defect was ameliorated, the mutated channels had biophysical properties consistent with long QT syndrome. The lack of phenotypic changes associated with the long QT syndrome could be explained by a T353I-induced trafficking defect reducing the number of mutant channels with persistent currents present at the sarcolemma.
Details
- Title: Subtitle
- A sodium channel pore mutation causing Brugada syndrome
- Creators
- Arnold E Pfahnl - Division of Cardiology, Atlanta Veterans Affairs Medical Center and Emory University, Atlanta, GeorgiaPrakash C Viswanathan - Cardiovascular Institute, University of Pittsburgh, Pittsburgh, PennsylvaniaRaul Weiss - Ohio State University, Dorothy M. Davis Heart and Lung Institute, Columbus, OhioLijuan L Shang - Division of Cardiology, Atlanta Veterans Affairs Medical Center and Emory University, Atlanta, GeorgiaShamarendra Sanyal - Division of Cardiology, Atlanta Veterans Affairs Medical Center and Emory University, Atlanta, GeorgiaVladimir Shusterman - Cardiovascular Institute, University of Pittsburgh, Pittsburgh, PennsylvaniaCari Kornblit - Cardiovascular Institute, University of Pittsburgh, Pittsburgh, PennsylvaniaBarry London - Cardiovascular Institute, University of Pittsburgh, Pittsburgh, PennsylvaniaSamuel C Dudley - Division of Cardiology, Atlanta Veterans Affairs Medical Center and Emory University, Atlanta, Georgia
- Resource Type
- Journal article
- Publication Details
- Heart rhythm, Vol.4(1), pp.46-53
- DOI
- 10.1016/j.hrthm.2006.09.031
- PMID
- 17198989
- PMCID
- PMC1779366
- NLM abbreviation
- Heart Rhythm
- ISSN
- 1547-5271
- eISSN
- 1556-3871
- Publisher
- Elsevier Inc
- Language
- English
- Date published
- 2007
- Academic Unit
- Molecular Physiology and Biophysics; Cardiovascular Medicine; Internal Medicine
- Record Identifier
- 9984025451702771
Metrics
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