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On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases
Voltage-gated sodium channels are intrinsic plasma membrane proteins that initiate the action potential in electrically excitable cells. They are composed of a pore-forming α-subunit and associated β-subunits. The β1-subunit was the first accessory subunit to be cloned. It can be important for contr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434899/ https://www.ncbi.nlm.nih.gov/pubmed/26042039 http://dx.doi.org/10.3389/fphar.2015.00108 |
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author | Baroni, Debora Moran, Oscar |
author_facet | Baroni, Debora Moran, Oscar |
author_sort | Baroni, Debora |
collection | PubMed |
description | Voltage-gated sodium channels are intrinsic plasma membrane proteins that initiate the action potential in electrically excitable cells. They are composed of a pore-forming α-subunit and associated β-subunits. The β1-subunit was the first accessory subunit to be cloned. It can be important for controlling cell excitability and modulating multiple aspects of sodium channel physiology. Mutations of β1 are implicated in a wide variety of inherited pathologies, including epilepsy and cardiac conduction diseases. This review summarizes β1-subunit related channelopathies pointing out the current knowledge concerning their genetic background and their underlying molecular mechanisms. |
format | Online Article Text |
id | pubmed-4434899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44348992015-06-03 On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases Baroni, Debora Moran, Oscar Front Pharmacol Pharmacology Voltage-gated sodium channels are intrinsic plasma membrane proteins that initiate the action potential in electrically excitable cells. They are composed of a pore-forming α-subunit and associated β-subunits. The β1-subunit was the first accessory subunit to be cloned. It can be important for controlling cell excitability and modulating multiple aspects of sodium channel physiology. Mutations of β1 are implicated in a wide variety of inherited pathologies, including epilepsy and cardiac conduction diseases. This review summarizes β1-subunit related channelopathies pointing out the current knowledge concerning their genetic background and their underlying molecular mechanisms. Frontiers Media S.A. 2015-05-18 /pmc/articles/PMC4434899/ /pubmed/26042039 http://dx.doi.org/10.3389/fphar.2015.00108 Text en Copyright © 2015 Baroni and Moran. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Baroni, Debora Moran, Oscar On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
title | On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
title_full | On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
title_fullStr | On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
title_full_unstemmed | On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
title_short | On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
title_sort | on the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434899/ https://www.ncbi.nlm.nih.gov/pubmed/26042039 http://dx.doi.org/10.3389/fphar.2015.00108 |
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