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The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma

Allergic asthma (AA) is a complex disorder with heterogeneous features of airway hyperresponsiveness, inflammation, and remodeling. The increase of airway smooth muscle (ASM) mass is a fundamental component of bronchial remodeling in AA, yet the pathophysiological mechanisms and clinical outcomes as...

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Autores principales: Shareef, Suhayla H., Amin, Kawa, Janson, Christer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139938/
https://www.ncbi.nlm.nih.gov/pubmed/33566255
http://dx.doi.org/10.1007/s10753-020-01401-y
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author Shareef, Suhayla H.
Amin, Kawa
Janson, Christer
author_facet Shareef, Suhayla H.
Amin, Kawa
Janson, Christer
author_sort Shareef, Suhayla H.
collection PubMed
description Allergic asthma (AA) is a complex disorder with heterogeneous features of airway hyperresponsiveness, inflammation, and remodeling. The increase of airway smooth muscle (ASM) mass is a fundamental component of bronchial remodeling in AA, yet the pathophysiological mechanisms and clinical outcomes associated with ASM modulation are still elusive. The objective of this study is to compare the expression level of β-dystroglycan (β-DG) in ASM in AA subjects and a healthy control group and to investigate the relationship between eosinophils and β-DG in ASM in patients with AA. Thirteen AA patients and seven control subjects were analyzed for the ASM area and eosinophil cells. Bronchial biopsies were stained by β-DG and eosinophil cationic protein (ECP) using immunohistochemistry. The proportion of ASM with β-DG staining was greater in those with AA than in the healthy control group (mean (95% CI) (28.3% (23.8–32.7%) vs. 16.4% (14.1–18.5%), P < 0.0001). The number of ECP positive cells was higher in patients with AA than in the control group (4056 (3819–4296) vs. 466 (395–537) cells/mm(2) P < 0.0001). In AA, the number of ECP positive cells was significantly correlated to the β-DG expression in ASM (r = 0.77, P = 0.002). There is an increased β-DG expression in ASM and a higher number of ECP positive cells in the bronchial biopsy of those with AA than those in the control group. The increased expression of β-DG in ASM in AA subjects correlates with the number of eosinophils, suggesting a role for this cell in airway remodeling in AA.
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spelling pubmed-81399382021-06-03 The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma Shareef, Suhayla H. Amin, Kawa Janson, Christer Inflammation Original Article Allergic asthma (AA) is a complex disorder with heterogeneous features of airway hyperresponsiveness, inflammation, and remodeling. The increase of airway smooth muscle (ASM) mass is a fundamental component of bronchial remodeling in AA, yet the pathophysiological mechanisms and clinical outcomes associated with ASM modulation are still elusive. The objective of this study is to compare the expression level of β-dystroglycan (β-DG) in ASM in AA subjects and a healthy control group and to investigate the relationship between eosinophils and β-DG in ASM in patients with AA. Thirteen AA patients and seven control subjects were analyzed for the ASM area and eosinophil cells. Bronchial biopsies were stained by β-DG and eosinophil cationic protein (ECP) using immunohistochemistry. The proportion of ASM with β-DG staining was greater in those with AA than in the healthy control group (mean (95% CI) (28.3% (23.8–32.7%) vs. 16.4% (14.1–18.5%), P < 0.0001). The number of ECP positive cells was higher in patients with AA than in the control group (4056 (3819–4296) vs. 466 (395–537) cells/mm(2) P < 0.0001). In AA, the number of ECP positive cells was significantly correlated to the β-DG expression in ASM (r = 0.77, P = 0.002). There is an increased β-DG expression in ASM and a higher number of ECP positive cells in the bronchial biopsy of those with AA than those in the control group. The increased expression of β-DG in ASM in AA subjects correlates with the number of eosinophils, suggesting a role for this cell in airway remodeling in AA. Springer US 2021-02-10 2021 /pmc/articles/PMC8139938/ /pubmed/33566255 http://dx.doi.org/10.1007/s10753-020-01401-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Original Article
Shareef, Suhayla H.
Amin, Kawa
Janson, Christer
The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma
title The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma
title_full The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma
title_fullStr The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma
title_full_unstemmed The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma
title_short The Association Between β-Dystroglycan in Airway Smooth Muscle and Eosinophils in Allergic Asthma
title_sort association between β-dystroglycan in airway smooth muscle and eosinophils in allergic asthma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139938/
https://www.ncbi.nlm.nih.gov/pubmed/33566255
http://dx.doi.org/10.1007/s10753-020-01401-y
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