Literature DB >> 26361848

The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology.

Christiaan C Veerman1, Arthur A M Wilde2, Elisabeth M Lodder3.   

Abstract

The gene SCN5A encodes the main cardiac sodium channel NaV1.5. This channel predominates the cardiac sodium current, INa, which underlies the fast upstroke of the cardiac action potential. As such, it plays a crucial role in cardiac electrophysiology. Over the last 60years a tremendous amount of knowledge regarding its function at the electrophysiological and molecular level has been acquired. Furthermore, genetic studies have shown that mutations in SCN5A are associated with multiple cardiac diseases (e.g. Brugada syndrome, Long QT syndrome, conduction disease and cardiomyopathy), while genetic variation in the general population has been associated with differences in cardiac conduction and risk of arrhythmia through genome wide association studies. In this review we aim to give an overview of the current knowledge (and the gaps therein) on SCN5A and NaV1.5.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26361848      PMCID: PMC6636349          DOI: 10.1016/j.gene.2015.08.062

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  134 in total

Review 1.  The cardiac sodium channel: gating function and molecular pharmacology.

Authors:  J R Balser
Journal:  J Mol Cell Cardiol       Date:  2001-04       Impact factor: 5.000

2.  Cardiac conduction defects associate with mutations in SCN5A.

Authors:  J J Schott; C Alshinawi; F Kyndt; V Probst; T M Hoorntje; M Hulsbeek; A A Wilde; D Escande; M M Mannens; H Le Marec
Journal:  Nat Genet       Date:  1999-09       Impact factor: 38.330

3.  A molecular link between the sudden infant death syndrome and the long-QT syndrome.

Authors:  P J Schwartz; S G Priori; R Dumaine; C Napolitano; C Antzelevitch; M Stramba-Badiale; T A Richard; M R Berti; R Bloise
Journal:  N Engl J Med       Date:  2000-07-27       Impact factor: 91.245

4.  A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

Authors:  C Bezzina; M W Veldkamp; M P van Den Berg; A V Postma; M B Rook; J W Viersma; I M van Langen; G Tan-Sindhunata; M T Bink-Boelkens; A H van Der Hout; M M Mannens; A A Wilde
Journal:  Circ Res       Date:  1999 Dec 3-17       Impact factor: 17.367

5.  Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

Authors:  M J Ackerman; B L Siu; W Q Sturner; D J Tester; C R Valdivia; J C Makielski; J A Towbin
Journal:  JAMA       Date:  2001-11-14       Impact factor: 56.272

6.  A sodium-channel mutation causes isolated cardiac conduction disease.

Authors:  H L Tan; M T Bink-Boelkens; C R Bezzina; P C Viswanathan; G C Beaufort-Krol; P J van Tintelen; M P van den Berg; A A Wilde; J R Balser
Journal:  Nature       Date:  2001-02-22       Impact factor: 49.962

7.  Sodium current in human jejunal circular smooth muscle cells.

Authors:  Adrian N Holm; Adam Rich; Steven M Miller; Peter Strege; Yijun Ou; SimonJ Gibbons; Michael G Sarr; Joseph H Szurszewski; James L Rae; Gianrico Farrugia
Journal:  Gastroenterology       Date:  2002-01       Impact factor: 22.682

8.  Contractile adaptations preserving cardiac output predispose the hypertrophied canine heart to delayed afterdepolarization-dependent ventricular arrhythmias.

Authors:  S H de Groot; M Schoenmakers; M M Molenschot; J D Leunissen; H J Wellens; M A Vos
Journal:  Circulation       Date:  2000-10-24       Impact factor: 29.690

9.  Distribution of a persistent sodium current across the ventricular wall in guinea pigs.

Authors:  B F Sakmann; A J Spindler; S M Bryant; K W Linz; D Noble
Journal:  Circ Res       Date:  2000-11-10       Impact factor: 17.367

10.  A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.

Authors:  J Akai; N Makita; H Sakurada; N Shirai; K Ueda; A Kitabatake; K Nakazawa; A Kimura; M Hiraoka
Journal:  FEBS Lett       Date:  2000-08-11       Impact factor: 4.124

View more
  52 in total

1.  Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval.

Authors:  Ashish Kapoor; Dongwon Lee; Luke Zhu; Elsayed Z Soliman; Megan L Grove; Eric Boerwinkle; Dan E Arking; Aravinda Chakravarti
Journal:  Proc Natl Acad Sci U S A       Date:  2019-05-08       Impact factor: 11.205

2.  Feasibility of analysis of the SCN5A gene in paraffin embedded samples in sudden infant death cases at the Pretoria Medico-Legal Laboratory, South Africa.

Authors:  Barbara Ströh van Deventer; Lorraine du Toit-Prinsloo; Chantal van Niekerk
Journal:  Forensic Sci Med Pathol       Date:  2018-06-16       Impact factor: 2.007

3.  Brugada syndrome trafficking-defective Nav1.5 channels can trap cardiac Kir2.1/2.2 channels.

Authors:  Marta Pérez-Hernández; Marcos Matamoros; Silvia Alfayate; Paloma Nieto-Marín; Raquel G Utrilla; David Tinaquero; Raquel de Andrés; Teresa Crespo; Daniela Ponce-Balbuena; B Cicero Willis; Eric N Jiménez-Vazquez; Guadalupe Guerrero-Serna; Andre M da Rocha; Katherine Campbell; Todd J Herron; F Javier Díez-Guerra; Juan Tamargo; José Jalife; Ricardo Caballero; Eva Delpón
Journal:  JCI Insight       Date:  2018-09-20

4.  Complexity of cardiac ion channel macromolecular complexes.

Authors:  Peter J Mohler; Hugues Abriel
Journal:  Cardiovasc Res       Date:  2016-03-16       Impact factor: 10.787

5.  Aberrant Expression of a Non-muscle RBFOX2 Isoform Triggers Cardiac Conduction Defects in Myotonic Dystrophy.

Authors:  Chaitali Misra; Sushant Bangru; Feikai Lin; Kin Lam; Sara N Koenig; Ellen R Lubbers; Jamila Hedhli; Nathaniel P Murphy; Darren J Parker; Lawrence W Dobrucki; Thomas A Cooper; Emad Tajkhorshid; Peter J Mohler; Auinash Kalsotra
Journal:  Dev Cell       Date:  2020-02-27       Impact factor: 12.270

Review 6.  Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.

Authors:  Ali J Marian; Eva van Rooij; Robert Roberts
Journal:  J Am Coll Cardiol       Date:  2016-12-27       Impact factor: 24.094

7.  Cardiomyocyte Expression of ZO-1 Is Essential for Normal Atrioventricular Conduction but Does Not Alter Ventricular Function.

Authors:  Kevin P Vincent; Angela K Peter; Jianlin Zhang; Matthew Klos; Hongqiang Cheng; Selina M Huang; Jordan K Towne; Debbie Ferng; Yusu Gu; Nancy D Dalton; Yunghang Chan; Ruixia Li; Kirk L Peterson; Ju Chen; Andrew D McCulloch; Kirk U Knowlton; Robert S Ross
Journal:  Circ Res       Date:  2020-04-29       Impact factor: 17.367

8.  The citrus flavanone hesperetin preferentially inhibits slow-inactivating currents of a long QT syndrome type 3 syndrome Na+ channel mutation.

Authors:  Julio Alvarez-Collazo; Alejandro López-Requena; Loipa Galán; Ariel Talavera; Julio L Alvarez; Karel Talavera
Journal:  Br J Pharmacol       Date:  2019-03-27       Impact factor: 8.739

9.  αB-Crystallin Interacts with Nav1.5 and Regulates Ubiquitination and Internalization of Cell Surface Nav1.5.

Authors:  Yuan Huang; Zhijie Wang; Yinan Liu; Hongbo Xiong; Yuanyuan Zhao; Ling Wu; Chao Yuan; Longfei Wang; Yuxi Hou; Gang Yu; Zhengrong Huang; Chengqi Xu; Qiuyun Chen; Qing K Wang
Journal:  J Biol Chem       Date:  2016-03-09       Impact factor: 5.157

10.  SCN5A (NaV1.5) Variant Functional Perturbation and Clinical Presentation: Variants of a Certain Significance.

Authors:  Brett M Kroncke; Andrew M Glazer; Derek K Smith; Jeffrey D Blume; Dan M Roden
Journal:  Circ Genom Precis Med       Date:  2018-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.