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The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death

The p38 mitogen-activated protein kinase (MAPK) is involved in a multitude of essential cellular processes. The kinase is activated in response to environmental stresses, including bacterial infections and inflammation, to regulate the immune response of the host. However, recent studies have demons...

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Detalles Bibliográficos
Autores principales: Gräb, Jessica, Rybniker, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657118/
https://www.ncbi.nlm.nih.gov/pubmed/31384128
http://dx.doi.org/10.1177/1178636119864594
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author Gräb, Jessica
Rybniker, Jan
author_facet Gräb, Jessica
Rybniker, Jan
author_sort Gräb, Jessica
collection PubMed
description The p38 mitogen-activated protein kinase (MAPK) is involved in a multitude of essential cellular processes. The kinase is activated in response to environmental stresses, including bacterial infections and inflammation, to regulate the immune response of the host. However, recent studies have demonstrated that pathogens can manipulate p38 MAPK signaling for their own benefit to either prevent or induce host cell apoptosis. In addition, there is evidence demonstrating that p38 MAPK is a potent trigger of pathogen-induced necrosis driven by mitochondrial membrane disruption. Given the large number of p38 MAPK inhibitors that have been tested in clinical trials, these findings provide an opportunity to repurpose these drugs for improved control of infectious diseases.
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spelling pubmed-66571182019-08-05 The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death Gräb, Jessica Rybniker, Jan Microbiol Insights Commentary The p38 mitogen-activated protein kinase (MAPK) is involved in a multitude of essential cellular processes. The kinase is activated in response to environmental stresses, including bacterial infections and inflammation, to regulate the immune response of the host. However, recent studies have demonstrated that pathogens can manipulate p38 MAPK signaling for their own benefit to either prevent or induce host cell apoptosis. In addition, there is evidence demonstrating that p38 MAPK is a potent trigger of pathogen-induced necrosis driven by mitochondrial membrane disruption. Given the large number of p38 MAPK inhibitors that have been tested in clinical trials, these findings provide an opportunity to repurpose these drugs for improved control of infectious diseases. SAGE Publications 2019-07-24 /pmc/articles/PMC6657118/ /pubmed/31384128 http://dx.doi.org/10.1177/1178636119864594 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Commentary
Gräb, Jessica
Rybniker, Jan
The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death
title The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death
title_full The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death
title_fullStr The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death
title_full_unstemmed The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death
title_short The Expanding Role of p38 Mitogen-Activated Protein Kinase in Programmed Host Cell Death
title_sort expanding role of p38 mitogen-activated protein kinase in programmed host cell death
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657118/
https://www.ncbi.nlm.nih.gov/pubmed/31384128
http://dx.doi.org/10.1177/1178636119864594
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