4.5 Article

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

Journal

INFLAMMATION
Volume 44, Issue 3, Pages 1060-1068

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10753-020-01401-y

Keywords

allergic asthma; airway smooth muscle; beta-dystroglycan; eosinophil; inflammation; remodeling

Funding

  1. Uppsala University
  2. University of Sulaimani, College of Medicine, Sulaimani, Iraq
  3. Uppsala University, Faculty of Medical Sciences, Department of Respiratory Medicine, Uppsala, Sweden
  4. Bror Hjerpstedts Foundation

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In individuals with allergic asthma, there is an increased expression of beta-dystroglycan in airway smooth muscle and a higher number of eosinophils compared to healthy individuals. This suggests a potential role for eosinophils in airway remodeling 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 associated with ASM modulation are still elusive. The objective of this study is to compare the expression level of beta-dystroglycan (beta-DG) in ASM in AA subjects and a healthy control group and to investigate the relationship between eosinophils and beta-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 beta-DG and eosinophil cationic protein (ECP) using immunohistochemistry. The proportion of ASM with beta-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 beta-DG expression in ASM (r = 0.77, P = 0.002). There is an increased beta-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 beta-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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