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Novel roles of PAK1 in the heart

Our work and others’ over the past few years have led to the identification of new roles of PAK1 in cardiac physiology, such as the regulation of cardiac ion channel and actomyosin function. More recent studies have revealed that PAK1-deficient mice were vulnerable to cardiac hypertrophy and readily...

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Detalles Bibliográficos
Autores principales: Ke, Yunbo, Lei, Ming, Wang, Xin, Solaro, R. John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490967/
https://www.ncbi.nlm.nih.gov/pubmed/23162741
http://dx.doi.org/10.4161/cl.21497
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author Ke, Yunbo
Lei, Ming
Wang, Xin
Solaro, R. John
author_facet Ke, Yunbo
Lei, Ming
Wang, Xin
Solaro, R. John
author_sort Ke, Yunbo
collection PubMed
description Our work and others’ over the past few years have led to the identification of new roles of PAK1 in cardiac physiology, such as the regulation of cardiac ion channel and actomyosin function. More recent studies have revealed that PAK1-deficient mice were vulnerable to cardiac hypertrophy and readily progress to failure under sustained pressure overload and susceptible to ischemia/reperfusion injury. Our further study indicated that the PAK1 activator FTY720 was able to prevent this pressure overload-induced hypertrophy in wild-type mice without compromising their cardiac functions. A cardiac protective effect against ischemia/reperfusion injury by FTY720 was also observed in both rat and mouse models by us and others. Thus, these studies suggest that PAK1 is more important in the heart than previously thought, in particular a therapeutic potential of PAK1 activators. In the future, in-depth investigations are required to further substantiate our hypotheses on mechanisms for PAK1 function in the heart and to explore a therapeutic potential of FTY720 and other PAK1 activators in heart disease conditions.
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spelling pubmed-34909672012-11-16 Novel roles of PAK1 in the heart Ke, Yunbo Lei, Ming Wang, Xin Solaro, R. John Cell Logist Review Our work and others’ over the past few years have led to the identification of new roles of PAK1 in cardiac physiology, such as the regulation of cardiac ion channel and actomyosin function. More recent studies have revealed that PAK1-deficient mice were vulnerable to cardiac hypertrophy and readily progress to failure under sustained pressure overload and susceptible to ischemia/reperfusion injury. Our further study indicated that the PAK1 activator FTY720 was able to prevent this pressure overload-induced hypertrophy in wild-type mice without compromising their cardiac functions. A cardiac protective effect against ischemia/reperfusion injury by FTY720 was also observed in both rat and mouse models by us and others. Thus, these studies suggest that PAK1 is more important in the heart than previously thought, in particular a therapeutic potential of PAK1 activators. In the future, in-depth investigations are required to further substantiate our hypotheses on mechanisms for PAK1 function in the heart and to explore a therapeutic potential of FTY720 and other PAK1 activators in heart disease conditions. Landes Bioscience 2012-04-01 /pmc/articles/PMC3490967/ /pubmed/23162741 http://dx.doi.org/10.4161/cl.21497 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Ke, Yunbo
Lei, Ming
Wang, Xin
Solaro, R. John
Novel roles of PAK1 in the heart
title Novel roles of PAK1 in the heart
title_full Novel roles of PAK1 in the heart
title_fullStr Novel roles of PAK1 in the heart
title_full_unstemmed Novel roles of PAK1 in the heart
title_short Novel roles of PAK1 in the heart
title_sort novel roles of pak1 in the heart
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490967/
https://www.ncbi.nlm.nih.gov/pubmed/23162741
http://dx.doi.org/10.4161/cl.21497
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