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Being there: cellular targeting of voltage-gated sodium channels in the heart

Voltage-gated sodium (Na(v)) channels in cardiomyocytes are localized in specialized membrane domains that optimize their functions in propagating action potentials across cell junctions and in stimulating voltage-gated calcium channels located in T tubules. Mutation of the ankyrin-binding site of N...

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Detalles Bibliográficos
Autores principales: Bennett, Vann, Healy, Jane
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213601/
https://www.ncbi.nlm.nih.gov/pubmed/18180365
http://dx.doi.org/10.1083/jcb.200712098
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author Bennett, Vann
Healy, Jane
author_facet Bennett, Vann
Healy, Jane
author_sort Bennett, Vann
collection PubMed
description Voltage-gated sodium (Na(v)) channels in cardiomyocytes are localized in specialized membrane domains that optimize their functions in propagating action potentials across cell junctions and in stimulating voltage-gated calcium channels located in T tubules. Mutation of the ankyrin-binding site of Na(v)1.5, the principal Na(v) channel in the heart, was previously known to cause cardiac arrhythmia and the retention of Na(v)1.5 in an intracellular compartment in cardiomyocytes. Conclusive evidence is now provided that direct interaction between Na(v)1.5 and ankyrin-G is necessary for the expression of Na(v)1.5 at the cardiomyocyte cell surface.
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spelling pubmed-22136012008-07-14 Being there: cellular targeting of voltage-gated sodium channels in the heart Bennett, Vann Healy, Jane J Cell Biol Reviews Voltage-gated sodium (Na(v)) channels in cardiomyocytes are localized in specialized membrane domains that optimize their functions in propagating action potentials across cell junctions and in stimulating voltage-gated calcium channels located in T tubules. Mutation of the ankyrin-binding site of Na(v)1.5, the principal Na(v) channel in the heart, was previously known to cause cardiac arrhythmia and the retention of Na(v)1.5 in an intracellular compartment in cardiomyocytes. Conclusive evidence is now provided that direct interaction between Na(v)1.5 and ankyrin-G is necessary for the expression of Na(v)1.5 at the cardiomyocyte cell surface. The Rockefeller University Press 2008-01-14 /pmc/articles/PMC2213601/ /pubmed/18180365 http://dx.doi.org/10.1083/jcb.200712098 Text en Copyright © 2008, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Reviews
Bennett, Vann
Healy, Jane
Being there: cellular targeting of voltage-gated sodium channels in the heart
title Being there: cellular targeting of voltage-gated sodium channels in the heart
title_full Being there: cellular targeting of voltage-gated sodium channels in the heart
title_fullStr Being there: cellular targeting of voltage-gated sodium channels in the heart
title_full_unstemmed Being there: cellular targeting of voltage-gated sodium channels in the heart
title_short Being there: cellular targeting of voltage-gated sodium channels in the heart
title_sort being there: cellular targeting of voltage-gated sodium channels in the heart
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213601/
https://www.ncbi.nlm.nih.gov/pubmed/18180365
http://dx.doi.org/10.1083/jcb.200712098
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