Literature DB >> 25721215

Nav1.5 channels can reach the plasma membrane through distinct N-glycosylation states.

Aurélie Mercier1, Romain Clément1, Thomas Harnois2, Nicolas Bourmeyster2, Patrick Bois1, Aurélien Chatelier3.   

Abstract

BACKGROUND: Like many voltage-gated sodium channels, the cardiac isoform Nav1.5 is well known as a glycoprotein which necessarily undergoes N-glycosylation processing during its transit to the plasma membrane. In some cardiac disorders, especially the Brugada syndrome (BrS), mutations in Nav1.5 encoding gene lead to intracellular retention and consequently trafficking defect of these proteins. We used two BrS mutants as tools to clarify both Nav1.5 glycosylation states and associated secretory behaviors.
METHODS: Patch-clamp recordings and surface biotinylation assays of HEK293T cells expressing wild-type (WT) and/or mutant Nav1.5 proteins were performed to assess the impact of mutant co-expression on the membrane activity and localization of WT channels. Enzymatic deglycosylation assays and brefeldin A (BFA) treatments were also employed to further characterize recombinant and native Nav1.5 maturation.
RESULTS: The present data demonstrate that Nav1.5 channels mainly exist as two differentially glycosylated forms. We reveal that dominant negative effects induced by BrS mutants upon WT channel current result from the abnormal surface expression of the fully-glycosylated forms exclusively. Furthermore, we show that core-glycosylated channels can be found at the surface membrane of BFA-treated or untreated cells, but obviously without generating any sodium current.
CONCLUSIONS: Our findings provide evidence that native and recombinant Nav1.5 subunits are expressed as two distinct matured forms. Fully-glycosylated state of Nav1.5 seems to determine its functionality whereas core-glycosylated forms might be transported to the plasma membrane through an unconventional Golgi-independent secretory route. GENERAL SIGNIFICANCE: This work highlights that N-linked glycosylation processing would be critical for Nav1.5 membrane trafficking and function.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Brugada syndrome; N-glycosylation; Na(v)1.5; Negative dominance; Secretory pathway; Voltage-gated sodium channel

Mesh:

Substances:

Year:  2015        PMID: 25721215     DOI: 10.1016/j.bbagen.2015.02.009

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  20 in total

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2.  Cardiac Kir2.1 and NaV1.5 Channels Traffic Together to the Sarcolemma to Control Excitability.

Authors:  Daniela Ponce-Balbuena; Guadalupe Guerrero-Serna; Carmen R Valdivia; Ricardo Caballero; F Javier Diez-Guerra; Eric N Jiménez-Vázquez; Rafael J Ramírez; André Monteiro da Rocha; Todd J Herron; Katherine F Campbell; B Cicero Willis; Francisco J Alvarado; Manuel Zarzoso; Kuljeet Kaur; Marta Pérez-Hernández; Marcos Matamoros; Héctor H Valdivia; Eva Delpón; José Jalife
Journal:  Circ Res       Date:  2018-03-07       Impact factor: 17.367

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.  N-Glycosylation of the voltage-gated sodium channel β2 subunit is required for efficient trafficking of NaV1.5/β2 to the plasma membrane.

Authors:  Eric Cortada; Ramon Brugada; Marcel Verges
Journal:  J Biol Chem       Date:  2019-09-11       Impact factor: 5.157

5.  SCN2A-related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects.

Authors:  Xiao-Ru Yang; Vamsi Krishna Murthy Ginjupalli; Olivier Theriault; Hugo Poulin; Juan Pablo Appendino; Ping Yee Billie Au; Mohamed Chahine
Journal:  J Neurophysiol       Date:  2022-04-13       Impact factor: 2.974

6.  Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder.

Authors:  Julie M Jones; Louise Dionne; James Dell'Orco; Rachel Parent; Jamie N Krueger; Xiaoyang Cheng; Sulayman D Dib-Hajj; Rosie K Bunton-Stasyshyn; Lisa M Sharkey; James J Dowling; Geoffrey G Murphy; Vikram G Shakkottai; Peter Shrager; Miriam H Meisler
Journal:  Neurobiol Dis       Date:  2016-01-22       Impact factor: 5.996

Review 7.  Endoplasmic reticulum stress in the heart: insights into mechanisms and drug targets.

Authors:  Shunyao Wang; Pablo Binder; Qiru Fang; Zhenzhong Wang; Wei Xiao; Wei Liu; Xin Wang
Journal:  Br J Pharmacol       Date:  2017-06-27       Impact factor: 8.739

Review 8.  Role for the Unfolded Protein Response in Heart Disease and Cardiac Arrhythmias.

Authors:  Man Liu; Samuel C Dudley
Journal:  Int J Mol Sci       Date:  2015-12-31       Impact factor: 5.923

9.  Molecular Chaperone Calnexin Regulates the Function of Drosophila Sodium Channel Paralytic.

Authors:  Xi Xiao; Changyan Chen; Tian-Ming Yu; Jiayao Ou; Menglong Rui; Yuanfen Zhai; Yijing He; Lei Xue; Margaret S Ho
Journal:  Front Mol Neurosci       Date:  2017-03-07       Impact factor: 5.639

Review 10.  An update on transcriptional and post-translational regulation of brain voltage-gated sodium channels.

Authors:  Donatus O Onwuli; Pedro Beltran-Alvarez
Journal:  Amino Acids       Date:  2015-10-27       Impact factor: 3.520

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