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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...

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Detalles Bibliográficos
Autores principales: Huetsch, John C., Suresh, Karthik, Shimoda, Larissa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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