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Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?

Our lungs are exposed daily to airborne pollutants, particulate matter, pathogens as well as lung allergens and irritants. Exposure to these substances can lead to inflammatory responses and may induce endogenous oxidant production, which can cause chronic inflammation, tissue damage and remodeling....

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Autores principales: van de Wetering, Cheryl, Elko, Evan, Berg, Marijn, Schiffers, Caspar H.J., Stylianidis, Vasili, van den Berge, Maarten, Nawijn, Martijn C., Wouters, Emiel F.M., Janssen-Heininger, Yvonne M.W., Reynaert, Niki L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131726/
https://www.ncbi.nlm.nih.gov/pubmed/33979767
http://dx.doi.org/10.1016/j.redox.2021.101995
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author van de Wetering, Cheryl
Elko, Evan
Berg, Marijn
Schiffers, Caspar H.J.
Stylianidis, Vasili
van den Berge, Maarten
Nawijn, Martijn C.
Wouters, Emiel F.M.
Janssen-Heininger, Yvonne M.W.
Reynaert, Niki L.
author_facet van de Wetering, Cheryl
Elko, Evan
Berg, Marijn
Schiffers, Caspar H.J.
Stylianidis, Vasili
van den Berge, Maarten
Nawijn, Martijn C.
Wouters, Emiel F.M.
Janssen-Heininger, Yvonne M.W.
Reynaert, Niki L.
author_sort van de Wetering, Cheryl
collection PubMed
description Our lungs are exposed daily to airborne pollutants, particulate matter, pathogens as well as lung allergens and irritants. Exposure to these substances can lead to inflammatory responses and may induce endogenous oxidant production, which can cause chronic inflammation, tissue damage and remodeling. Notably, the development of asthma and Chronic Obstructive Pulmonary Disease (COPD) is linked to the aforementioned irritants. Some inhaled foreign chemical compounds are rapidly absorbed and processed by phase I and II enzyme systems critical in the detoxification of xenobiotics including the glutathione-conjugating enzymes Glutathione S-transferases (GSTs). GSTs, and in particular genetic variants of GSTs that alter their activities, have been found to be implicated in the susceptibility to and progression of these lung diseases. Beyond their roles in phase II metabolism, evidence suggests that GSTs are also important mediators of normal lung growth. Therefore, the contribution of GSTs to the development of lung diseases in adults may already start in utero, and continues through infancy, childhood, and adult life. GSTs are also known to scavenge oxidants and affect signaling pathways by protein-protein interaction. Moreover, GSTs regulate reversible oxidative post-translational modifications of proteins, known as protein S-glutathionylation. Therefore, GSTs display an array of functions that impact the pathogenesis of asthma and COPD. In this review we will provide an overview of the specific functions of each class of mammalian cytosolic GSTs. This is followed by a comprehensive analysis of their expression profiles in the lung in healthy subjects, as well as alterations that have been described in (epithelial cells of) asthmatics and COPD patients. Particular emphasis is placed on the emerging evidence of the regulatory properties of GSTs beyond detoxification and their contribution to (un)healthy lungs throughout life. By providing a more thorough understanding, tailored therapeutic strategies can be designed to affect specific functions of particular GSTs.
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spelling pubmed-81317262021-05-21 Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility? van de Wetering, Cheryl Elko, Evan Berg, Marijn Schiffers, Caspar H.J. Stylianidis, Vasili van den Berge, Maarten Nawijn, Martijn C. Wouters, Emiel F.M. Janssen-Heininger, Yvonne M.W. Reynaert, Niki L. Redox Biol Articles from the Special Issue on Low Molecular Weight Thiols: Lessons Learned and New Perspectives; Edited by Dr. Barry Halliwell and Dr. Ivan Gout Our lungs are exposed daily to airborne pollutants, particulate matter, pathogens as well as lung allergens and irritants. Exposure to these substances can lead to inflammatory responses and may induce endogenous oxidant production, which can cause chronic inflammation, tissue damage and remodeling. Notably, the development of asthma and Chronic Obstructive Pulmonary Disease (COPD) is linked to the aforementioned irritants. Some inhaled foreign chemical compounds are rapidly absorbed and processed by phase I and II enzyme systems critical in the detoxification of xenobiotics including the glutathione-conjugating enzymes Glutathione S-transferases (GSTs). GSTs, and in particular genetic variants of GSTs that alter their activities, have been found to be implicated in the susceptibility to and progression of these lung diseases. Beyond their roles in phase II metabolism, evidence suggests that GSTs are also important mediators of normal lung growth. Therefore, the contribution of GSTs to the development of lung diseases in adults may already start in utero, and continues through infancy, childhood, and adult life. GSTs are also known to scavenge oxidants and affect signaling pathways by protein-protein interaction. Moreover, GSTs regulate reversible oxidative post-translational modifications of proteins, known as protein S-glutathionylation. Therefore, GSTs display an array of functions that impact the pathogenesis of asthma and COPD. In this review we will provide an overview of the specific functions of each class of mammalian cytosolic GSTs. This is followed by a comprehensive analysis of their expression profiles in the lung in healthy subjects, as well as alterations that have been described in (epithelial cells of) asthmatics and COPD patients. Particular emphasis is placed on the emerging evidence of the regulatory properties of GSTs beyond detoxification and their contribution to (un)healthy lungs throughout life. By providing a more thorough understanding, tailored therapeutic strategies can be designed to affect specific functions of particular GSTs. Elsevier 2021-05-02 /pmc/articles/PMC8131726/ /pubmed/33979767 http://dx.doi.org/10.1016/j.redox.2021.101995 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles from the Special Issue on Low Molecular Weight Thiols: Lessons Learned and New Perspectives; Edited by Dr. Barry Halliwell and Dr. Ivan Gout
van de Wetering, Cheryl
Elko, Evan
Berg, Marijn
Schiffers, Caspar H.J.
Stylianidis, Vasili
van den Berge, Maarten
Nawijn, Martijn C.
Wouters, Emiel F.M.
Janssen-Heininger, Yvonne M.W.
Reynaert, Niki L.
Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?
title Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?
title_full Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?
title_fullStr Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?
title_full_unstemmed Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?
title_short Glutathione S-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: Early life susceptibility?
title_sort glutathione s-transferases and their implications in the lung diseases asthma and chronic obstructive pulmonary disease: early life susceptibility?
topic Articles from the Special Issue on Low Molecular Weight Thiols: Lessons Learned and New Perspectives; Edited by Dr. Barry Halliwell and Dr. Ivan Gout
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131726/
https://www.ncbi.nlm.nih.gov/pubmed/33979767
http://dx.doi.org/10.1016/j.redox.2021.101995
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