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New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry

Several studies have shown the importance of oxidative stress (OS) in respiratory disease pathogenesis. It has been reported that the nasal epithelium may act as a surrogate for the bronchial epithelium in several respiratory diseases involving OS. However, the sample yields obtained from nasal biop...

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Autores principales: Reula, Ana, Pellicer, Daniel, Castillo, Silvia, Magallón, María, Armengot, Miguel, Herrera, Guadalupe, O’Connor, José-Enrique, Bañuls, Lucía, Navarro-García, María Mercedes, Escribano, Amparo, Dasí, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998408/
https://www.ncbi.nlm.nih.gov/pubmed/33799667
http://dx.doi.org/10.3390/jcm10061172
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author Reula, Ana
Pellicer, Daniel
Castillo, Silvia
Magallón, María
Armengot, Miguel
Herrera, Guadalupe
O’Connor, José-Enrique
Bañuls, Lucía
Navarro-García, María Mercedes
Escribano, Amparo
Dasí, Francisco
author_facet Reula, Ana
Pellicer, Daniel
Castillo, Silvia
Magallón, María
Armengot, Miguel
Herrera, Guadalupe
O’Connor, José-Enrique
Bañuls, Lucía
Navarro-García, María Mercedes
Escribano, Amparo
Dasí, Francisco
author_sort Reula, Ana
collection PubMed
description Several studies have shown the importance of oxidative stress (OS) in respiratory disease pathogenesis. It has been reported that the nasal epithelium may act as a surrogate for the bronchial epithelium in several respiratory diseases involving OS. However, the sample yields obtained from nasal biopsies are modest, limiting the number of parameters that can be determined. Flow cytometry has been widely used to evaluate cellular OS profiles. It has the advantage that analyses can be performed using a small amount of sample. Therefore, we aimed to set up a new method based on flow cytometry to assess the oxidative profile of human nasal epithelial cells which could be used in research on respiratory diseases. Levels of total nitric oxide, superoxide anion, peroxynitrite, and intracellular peroxides were measured. Reduced thiol levels, such as antioxidant-reduced glutathione and oxidative damaged lipids and proteins, were also analysed. The intracellular calcium levels, plasma membrane potential, apoptosis, and percentage of live cells were also studied. Finally, a strategy to evaluate the mitochondrial function, including mitochondrial hydrogen peroxide, superoxide anion, mitochondrial mass, and membrane potential, was set up. Using small amounts of sample and a non-invasive sampling technique, the described method enables the measurement of a comprehensive set of OS parameters in nasal epithelial cells, which could be useful in research on respiratory diseases.
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spelling pubmed-79984082021-03-28 New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry Reula, Ana Pellicer, Daniel Castillo, Silvia Magallón, María Armengot, Miguel Herrera, Guadalupe O’Connor, José-Enrique Bañuls, Lucía Navarro-García, María Mercedes Escribano, Amparo Dasí, Francisco J Clin Med Article Several studies have shown the importance of oxidative stress (OS) in respiratory disease pathogenesis. It has been reported that the nasal epithelium may act as a surrogate for the bronchial epithelium in several respiratory diseases involving OS. However, the sample yields obtained from nasal biopsies are modest, limiting the number of parameters that can be determined. Flow cytometry has been widely used to evaluate cellular OS profiles. It has the advantage that analyses can be performed using a small amount of sample. Therefore, we aimed to set up a new method based on flow cytometry to assess the oxidative profile of human nasal epithelial cells which could be used in research on respiratory diseases. Levels of total nitric oxide, superoxide anion, peroxynitrite, and intracellular peroxides were measured. Reduced thiol levels, such as antioxidant-reduced glutathione and oxidative damaged lipids and proteins, were also analysed. The intracellular calcium levels, plasma membrane potential, apoptosis, and percentage of live cells were also studied. Finally, a strategy to evaluate the mitochondrial function, including mitochondrial hydrogen peroxide, superoxide anion, mitochondrial mass, and membrane potential, was set up. Using small amounts of sample and a non-invasive sampling technique, the described method enables the measurement of a comprehensive set of OS parameters in nasal epithelial cells, which could be useful in research on respiratory diseases. MDPI 2021-03-11 /pmc/articles/PMC7998408/ /pubmed/33799667 http://dx.doi.org/10.3390/jcm10061172 Text en © 2021 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 Article
Reula, Ana
Pellicer, Daniel
Castillo, Silvia
Magallón, María
Armengot, Miguel
Herrera, Guadalupe
O’Connor, José-Enrique
Bañuls, Lucía
Navarro-García, María Mercedes
Escribano, Amparo
Dasí, Francisco
New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry
title New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry
title_full New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry
title_fullStr New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry
title_full_unstemmed New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry
title_short New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry
title_sort new laboratory protocol to determine the oxidative stress profile of human nasal epithelial cells using flow cytometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998408/
https://www.ncbi.nlm.nih.gov/pubmed/33799667
http://dx.doi.org/10.3390/jcm10061172
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