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Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension
Hyperproliferation of pulmonary arterial smooth muscle cells is a key component of vascular remodeling in the setting of pulmonary hypertension (PH). Numerous studies have explored factors governing the changes in smooth muscle cell phenotype that lead to the increased wall thickness, and have ident...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466559/ https://www.ncbi.nlm.nih.gov/pubmed/30841544 http://dx.doi.org/10.3390/antiox8030056 |
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author | Huetsch, John C. Suresh, Karthik Shimoda, Larissa A. |
author_facet | Huetsch, John C. Suresh, Karthik Shimoda, Larissa A. |
author_sort | Huetsch, John C. |
collection | PubMed |
description | Hyperproliferation of pulmonary arterial smooth muscle cells is a key component of vascular remodeling in the setting of pulmonary hypertension (PH). Numerous studies have explored factors governing the changes in smooth muscle cell phenotype that lead to the increased wall thickness, and have identified various potential candidates. A role for reactive oxygen species (ROS) has been well documented in PH. ROS can be generated from a variety of sources, including mitochondria, uncoupled nitric oxide synthase, xanthine oxidase, and reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. In this article, we will review recent data supporting a role for ROS generated from NADPH oxidases in promoting pulmonary arterial smooth muscle cell proliferation during PH. |
format | Online Article Text |
id | pubmed-6466559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64665592019-04-18 Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension Huetsch, John C. Suresh, Karthik Shimoda, Larissa A. Antioxidants (Basel) Review Hyperproliferation of pulmonary arterial smooth muscle cells is a key component of vascular remodeling in the setting of pulmonary hypertension (PH). Numerous studies have explored factors governing the changes in smooth muscle cell phenotype that lead to the increased wall thickness, and have identified various potential candidates. A role for reactive oxygen species (ROS) has been well documented in PH. ROS can be generated from a variety of sources, including mitochondria, uncoupled nitric oxide synthase, xanthine oxidase, and reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. In this article, we will review recent data supporting a role for ROS generated from NADPH oxidases in promoting pulmonary arterial smooth muscle cell proliferation during PH. MDPI 2019-03-05 /pmc/articles/PMC6466559/ /pubmed/30841544 http://dx.doi.org/10.3390/antiox8030056 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 Huetsch, John C. Suresh, Karthik Shimoda, Larissa A. Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension |
title | Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension |
title_full | Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension |
title_fullStr | Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension |
title_full_unstemmed | Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension |
title_short | Regulation of Smooth Muscle Cell Proliferation by NADPH Oxidases in Pulmonary Hypertension |
title_sort | regulation of smooth muscle cell proliferation by nadph oxidases in pulmonary hypertension |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466559/ https://www.ncbi.nlm.nih.gov/pubmed/30841544 http://dx.doi.org/10.3390/antiox8030056 |
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