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Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation
The control of vascular smooth muscle contractility enables regulation of blood pressure, which is paramount in physiological adaptation to environmental challenges. Maintenance of stable blood pressure is crucial for health as deregulation (caused by high or low blood pressure) leads to disease pro...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274199/ https://www.ncbi.nlm.nih.gov/pubmed/22319269 http://dx.doi.org/10.3390/s100402731 |
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author | Burgoyne, Joseph R. Eaton, Philip |
author_facet | Burgoyne, Joseph R. Eaton, Philip |
author_sort | Burgoyne, Joseph R. |
collection | PubMed |
description | The control of vascular smooth muscle contractility enables regulation of blood pressure, which is paramount in physiological adaptation to environmental challenges. Maintenance of stable blood pressure is crucial for health as deregulation (caused by high or low blood pressure) leads to disease progression. Vasotone is principally controlled by the cyclic nucleotide dependent protein kinases A and G, which regulate intracellular calcium and contractile protein calcium sensitivity. The classical pathways for activation of these two kinases are well established and involve the formation and activation by specific cyclic nucleotide second messengers. Recently we reported that both PKA and PKG can be regulated independently of their respective cyclic nucleotides via a mechanism whereby the kinases sense cellular oxidant production using redox active thiols. This novel redox regulation of these kinases is potentially of physiological importance, and may synergise with the classical regulatory mechanisms. |
format | Online Article Text |
id | pubmed-3274199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-32741992012-02-08 Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation Burgoyne, Joseph R. Eaton, Philip Sensors (Basel) Review The control of vascular smooth muscle contractility enables regulation of blood pressure, which is paramount in physiological adaptation to environmental challenges. Maintenance of stable blood pressure is crucial for health as deregulation (caused by high or low blood pressure) leads to disease progression. Vasotone is principally controlled by the cyclic nucleotide dependent protein kinases A and G, which regulate intracellular calcium and contractile protein calcium sensitivity. The classical pathways for activation of these two kinases are well established and involve the formation and activation by specific cyclic nucleotide second messengers. Recently we reported that both PKA and PKG can be regulated independently of their respective cyclic nucleotides via a mechanism whereby the kinases sense cellular oxidant production using redox active thiols. This novel redox regulation of these kinases is potentially of physiological importance, and may synergise with the classical regulatory mechanisms. Molecular Diversity Preservation International (MDPI) 2010-03-26 /pmc/articles/PMC3274199/ /pubmed/22319269 http://dx.doi.org/10.3390/s100402731 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Burgoyne, Joseph R. Eaton, Philip Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation |
title | Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation |
title_full | Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation |
title_fullStr | Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation |
title_full_unstemmed | Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation |
title_short | Oxidant Sensing by Protein Kinases A and G Enables Integration of Cell Redox State with Phosphoregulation |
title_sort | oxidant sensing by protein kinases a and g enables integration of cell redox state with phosphoregulation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274199/ https://www.ncbi.nlm.nih.gov/pubmed/22319269 http://dx.doi.org/10.3390/s100402731 |
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