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Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling

The cardiac fibroblast is a remarkably versatile cell type that coordinates inflammatory, fibrotic and hypertrophic responses in the heart through a complex array of intracellular and intercellular signaling mechanisms. One important signaling node that has been identified involves p38 MAPK; a famil...

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Detalles Bibliográficos
Autores principales: Turner, Neil A., Blythe, Nicola M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787752/
https://www.ncbi.nlm.nih.gov/pubmed/31394846
http://dx.doi.org/10.3390/jcdd6030027
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author Turner, Neil A.
Blythe, Nicola M.
author_facet Turner, Neil A.
Blythe, Nicola M.
author_sort Turner, Neil A.
collection PubMed
description The cardiac fibroblast is a remarkably versatile cell type that coordinates inflammatory, fibrotic and hypertrophic responses in the heart through a complex array of intracellular and intercellular signaling mechanisms. One important signaling node that has been identified involves p38 MAPK; a family of kinases activated in response to stress and inflammatory stimuli that modulates multiple aspects of cardiac fibroblast function, including inflammatory responses, myofibroblast differentiation, extracellular matrix turnover and the paracrine induction of cardiomyocyte hypertrophy. This review explores the emerging importance of the p38 MAPK pathway in cardiac fibroblasts, describes the molecular mechanisms by which it regulates the expression of key genes, and highlights its potential as a therapeutic target for reducing adverse myocardial remodeling.
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spelling pubmed-67877522019-10-16 Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling Turner, Neil A. Blythe, Nicola M. J Cardiovasc Dev Dis Review The cardiac fibroblast is a remarkably versatile cell type that coordinates inflammatory, fibrotic and hypertrophic responses in the heart through a complex array of intracellular and intercellular signaling mechanisms. One important signaling node that has been identified involves p38 MAPK; a family of kinases activated in response to stress and inflammatory stimuli that modulates multiple aspects of cardiac fibroblast function, including inflammatory responses, myofibroblast differentiation, extracellular matrix turnover and the paracrine induction of cardiomyocyte hypertrophy. This review explores the emerging importance of the p38 MAPK pathway in cardiac fibroblasts, describes the molecular mechanisms by which it regulates the expression of key genes, and highlights its potential as a therapeutic target for reducing adverse myocardial remodeling. MDPI 2019-08-07 /pmc/articles/PMC6787752/ /pubmed/31394846 http://dx.doi.org/10.3390/jcdd6030027 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Turner, Neil A.
Blythe, Nicola M.
Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
title Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
title_full Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
title_fullStr Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
title_full_unstemmed Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
title_short Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
title_sort cardiac fibroblast p38 mapk: a critical regulator of myocardial remodeling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787752/
https://www.ncbi.nlm.nih.gov/pubmed/31394846
http://dx.doi.org/10.3390/jcdd6030027
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