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Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels

Voltage-gated Kv7 potassium channels, encoded by KCNQ genes, have major physiological impacts cardiac myocytes, neurons, epithelial cells, and smooth muscle cells. Cyclic adenosine monophosphate (cAMP), a well-known intracellular secondary messenger, can activate numerous downstream effector protein...

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Autores principales: van der Horst, Jennifer, Greenwood, Iain A., Jepps, Thomas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338754/
https://www.ncbi.nlm.nih.gov/pubmed/32695022
http://dx.doi.org/10.3389/fphys.2020.00727
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author van der Horst, Jennifer
Greenwood, Iain A.
Jepps, Thomas A.
author_facet van der Horst, Jennifer
Greenwood, Iain A.
Jepps, Thomas A.
author_sort van der Horst, Jennifer
collection PubMed
description Voltage-gated Kv7 potassium channels, encoded by KCNQ genes, have major physiological impacts cardiac myocytes, neurons, epithelial cells, and smooth muscle cells. Cyclic adenosine monophosphate (cAMP), a well-known intracellular secondary messenger, can activate numerous downstream effector proteins, generating downstream signaling pathways that regulate many functions in cells. A role for cAMP in ion channel regulation has been established, and recent findings show that cAMP signaling plays a role in Kv7 channel regulation. Although cAMP signaling is recognized to regulate Kv7 channels, the precise molecular mechanism behind the cAMP-dependent regulation of Kv7 channels is complex. This review will summarize recent research findings that support the mechanisms of cAMP-dependent regulation of Kv7 channels.
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spelling pubmed-73387542020-07-20 Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels van der Horst, Jennifer Greenwood, Iain A. Jepps, Thomas A. Front Physiol Physiology Voltage-gated Kv7 potassium channels, encoded by KCNQ genes, have major physiological impacts cardiac myocytes, neurons, epithelial cells, and smooth muscle cells. Cyclic adenosine monophosphate (cAMP), a well-known intracellular secondary messenger, can activate numerous downstream effector proteins, generating downstream signaling pathways that regulate many functions in cells. A role for cAMP in ion channel regulation has been established, and recent findings show that cAMP signaling plays a role in Kv7 channel regulation. Although cAMP signaling is recognized to regulate Kv7 channels, the precise molecular mechanism behind the cAMP-dependent regulation of Kv7 channels is complex. This review will summarize recent research findings that support the mechanisms of cAMP-dependent regulation of Kv7 channels. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7338754/ /pubmed/32695022 http://dx.doi.org/10.3389/fphys.2020.00727 Text en Copyright © 2020 van der Horst, Greenwood and Jepps. 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) and the copyright owner(s) 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 Physiology
van der Horst, Jennifer
Greenwood, Iain A.
Jepps, Thomas A.
Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels
title Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels
title_full Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels
title_fullStr Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels
title_full_unstemmed Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels
title_short Cyclic AMP-Dependent Regulation of Kv7 Voltage-Gated Potassium Channels
title_sort cyclic amp-dependent regulation of kv7 voltage-gated potassium channels
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338754/
https://www.ncbi.nlm.nih.gov/pubmed/32695022
http://dx.doi.org/10.3389/fphys.2020.00727
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