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Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model

BACKGROUND: Airway obstruction (AO) in asthma is driven by airway smooth muscle (ASM) contraction. AO can be induced extrinsically by direct stimulation of ASM with contractile agonists as histamine, or by indirect provocation with antigens as ovalbumin, while the airway tone is dependent on intrins...

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Autores principales: Álvarez-Santos, Mayra D., Álvarez-González, Marisol, Eslava-De-Jesus, Elizabeth, González-López, Angel, Pacheco-Alba, Ivonne, Pérez-Del-Valle, Yazmín, Rojas-Madrid, Rodrigo, Bazán-Perkins, Blanca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753847/
https://www.ncbi.nlm.nih.gov/pubmed/35016714
http://dx.doi.org/10.1186/s13223-022-00645-7
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author Álvarez-Santos, Mayra D.
Álvarez-González, Marisol
Eslava-De-Jesus, Elizabeth
González-López, Angel
Pacheco-Alba, Ivonne
Pérez-Del-Valle, Yazmín
Rojas-Madrid, Rodrigo
Bazán-Perkins, Blanca
author_facet Álvarez-Santos, Mayra D.
Álvarez-González, Marisol
Eslava-De-Jesus, Elizabeth
González-López, Angel
Pacheco-Alba, Ivonne
Pérez-Del-Valle, Yazmín
Rojas-Madrid, Rodrigo
Bazán-Perkins, Blanca
author_sort Álvarez-Santos, Mayra D.
collection PubMed
description BACKGROUND: Airway obstruction (AO) in asthma is driven by airway smooth muscle (ASM) contraction. AO can be induced extrinsically by direct stimulation of ASM with contractile agonists as histamine, or by indirect provocation with antigens as ovalbumin, while the airway tone is dependent on intrinsic mechanisms. The association of the ASM phenotypes involved in different types of AO and airway tone in guinea pigs was evaluated. METHODS: Guinea pigs were sensitized to ovalbumin and challenged with antigen. In each challenge, the maximum OA response to ovalbumin was determined, and before the challenges, the tone of the airways. At third challenge, airway responsiveness (AR) to histamine was evaluated and ASM cells from trachea were disaggregated to determinate: (a) by flow cytometry, the percentage of cells that express transforming growth factor-β1 (TGF-β1), interleukin-13 (IL-13) and sarco-endoplasmic Ca(2+) ATPase-2b (SERCA2b), (b) by RT-PCR, the SERCA2B gene expression, (c) by ELISA, reduced glutathione (GSH) and, (d) Ca(2+) sarcoplasmic reticulum refilling rate by microfluorometry. Control guinea pig group received saline instead ovalbumin. RESULTS: Antigenic challenges in sensitized guinea pigs induced indirect AO, AR to histamine and increment in airway tone at third challenge. No relationship was observed between AO induced by antigen and AR to histamine with changes in airway tone. The extent of antigen-induced AO was associated with both, TGF-β1 expression in ASM and AR degree. The magnitude of AR and antigen-induced AO showed an inverse correlation with GSH levels in ASM. The airway tone showed an inverse association with SERCA2b expression. CONCLUSIONS: Our data suggest that each type of AO and airway tone depends on different ASM phenotypes: direct and indirect AO seems to be sensitive to the level of oxidative stress; indirect obstruction induced by antigen appears to be influenced by the expression of TGF-β1 and the SERCA2b expression level plays a role in the airway tone.
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spelling pubmed-87538472022-01-12 Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model Álvarez-Santos, Mayra D. Álvarez-González, Marisol Eslava-De-Jesus, Elizabeth González-López, Angel Pacheco-Alba, Ivonne Pérez-Del-Valle, Yazmín Rojas-Madrid, Rodrigo Bazán-Perkins, Blanca Allergy Asthma Clin Immunol Research BACKGROUND: Airway obstruction (AO) in asthma is driven by airway smooth muscle (ASM) contraction. AO can be induced extrinsically by direct stimulation of ASM with contractile agonists as histamine, or by indirect provocation with antigens as ovalbumin, while the airway tone is dependent on intrinsic mechanisms. The association of the ASM phenotypes involved in different types of AO and airway tone in guinea pigs was evaluated. METHODS: Guinea pigs were sensitized to ovalbumin and challenged with antigen. In each challenge, the maximum OA response to ovalbumin was determined, and before the challenges, the tone of the airways. At third challenge, airway responsiveness (AR) to histamine was evaluated and ASM cells from trachea were disaggregated to determinate: (a) by flow cytometry, the percentage of cells that express transforming growth factor-β1 (TGF-β1), interleukin-13 (IL-13) and sarco-endoplasmic Ca(2+) ATPase-2b (SERCA2b), (b) by RT-PCR, the SERCA2B gene expression, (c) by ELISA, reduced glutathione (GSH) and, (d) Ca(2+) sarcoplasmic reticulum refilling rate by microfluorometry. Control guinea pig group received saline instead ovalbumin. RESULTS: Antigenic challenges in sensitized guinea pigs induced indirect AO, AR to histamine and increment in airway tone at third challenge. No relationship was observed between AO induced by antigen and AR to histamine with changes in airway tone. The extent of antigen-induced AO was associated with both, TGF-β1 expression in ASM and AR degree. The magnitude of AR and antigen-induced AO showed an inverse correlation with GSH levels in ASM. The airway tone showed an inverse association with SERCA2b expression. CONCLUSIONS: Our data suggest that each type of AO and airway tone depends on different ASM phenotypes: direct and indirect AO seems to be sensitive to the level of oxidative stress; indirect obstruction induced by antigen appears to be influenced by the expression of TGF-β1 and the SERCA2b expression level plays a role in the airway tone. BioMed Central 2022-01-11 /pmc/articles/PMC8753847/ /pubmed/35016714 http://dx.doi.org/10.1186/s13223-022-00645-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Álvarez-Santos, Mayra D.
Álvarez-González, Marisol
Eslava-De-Jesus, Elizabeth
González-López, Angel
Pacheco-Alba, Ivonne
Pérez-Del-Valle, Yazmín
Rojas-Madrid, Rodrigo
Bazán-Perkins, Blanca
Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
title Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
title_full Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
title_fullStr Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
title_full_unstemmed Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
title_short Role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
title_sort role of airway smooth muscle cell phenotypes in airway tone and obstruction in guinea pig asthma model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753847/
https://www.ncbi.nlm.nih.gov/pubmed/35016714
http://dx.doi.org/10.1186/s13223-022-00645-7
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