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Eosinophils Promote Epithelial to Mesenchymal Transition of Bronchial Epithelial Cells

Authors :
Yasukawa, Atsushi
Hosoki, Koa
Toda, Masaaki
Miyake, Yasushi
Matsushima, Yuki
Matsumoto, Takahiro
Boveda-Ruiz, Daniel
Gil-Bernabe, Paloma
Nagao, Mizuho
Sugimoto, Mayumi
Hiraguchi, Yukiko
Tokuda, Reiko
Naito, Masahiro
Takagi, Takehiro
D'Alessandro-Gabazza, Corina N.
Suga, Shigeru
Kobayashi, Tetsu
Fujisawa, Takao
Taguchi, Osamu
Gabazza, Esteban C.
Source :
PLoS ONE. May2013, Vol. 8 Issue 5, p1-12. 12p.
Publication Year :
2013

Abstract

Eosinophilic inflammation and remodeling of the airways including subepithelial fibrosis and myofibroblast hyperplasia are characteristic pathological findings of bronchial asthma. Epithelial to mesenchymal transition (EMT) plays a critical role in airway remodelling. In this study, we hypothesized that infiltrating eosinophils promote airway remodelling in bronchial asthma. To demonstrate this hypothesis we evaluated the effect of eosinophils on EMT by in vitro and in vivo studies. EMT was assessed in mice that received intra-tracheal instillation of mouse bone marrow derived eosinophils and in human bronchial epithelial cells co-cultured with eosinophils freshly purified from healthy individuals or with eosinophilic leukemia cell lines. Intra-tracheal instillation of eosinophils was associated with enhanced bronchial inflammation and fibrosis and increased lung concentration of growth factors. Mice instilled with eosinophils pre-treated with transforming growth factor(TGF)-β1 siRNA had decreased bronchial wall fibrosis compared to controls. EMT was induced in bronchial epithelial cells co-cultured with human eosinophils and it was associated with increased expression of TGF-β1 and Smad3 phosphorylation in the bronchial epithelial cells. Treatment with anti-TGF-β1 antibody blocked EMT in bronchial epithelial cells. Eosinophils induced EMT in bronchial epithelial cells, suggesting their contribution to the pathogenesis of airway remodelling. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
8
Issue :
5
Database :
Academic Search Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
88376643
Full Text :
https://doi.org/10.1371/journal.pone.0064281