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Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro .

Authors :
Nishihara F
Nakagome K
Kobayashi T
Noguchi T
Araki R
Uchida Y
Soma T
Nagata M
Source :
ERJ open research [ERJ Open Res] 2015 Dec 22; Vol. 1 (2). Date of Electronic Publication: 2015 Dec 22 (Print Publication: 2015).
Publication Year :
2015

Abstract

In the airways of severe asthmatics, an increase of neutrophils and eosinophils is often observed despite high-dose corticosteroid therapy. We previously reported that interleukin-8-stimulated neutrophils induced trans-basement membrane migration (TBM) of eosinophils, suggesting the link between neutrophils and eosinophils. Concentrations of lipopolysaccharide (LPS) in the airway increase in severe asthma. As neutrophils express Toll-like receptor (TLR)4 and can release chemoattractants for eosinophils, we investigated whether LPS-stimulated neutrophils modify eosinophil TBM. Neutrophils and eosinophils were isolated from peripheral blood of healthy volunteers and severe asthmatics. Eosinophil TBM was examined using a modified Boyden's chamber technique. Eosinophils were added to the upper compartment, and neutrophils and LPS were added to the lower compartment. Migrated eosinophils were measured by eosinophil peroxidase assays. LPS-stimulated neutrophils induced eosinophil TBM (about 10-fold increase), although LPS or neutrophils alone did not. A leukotriene B <subscript>4</subscript> receptor antagonist, a platelet-activating factor receptor antagonist or an anti-TLR4 antibody decreased eosinophil TBM enhanced by LPS-stimulated neutrophils by almost half. Neutrophils from severe asthmatics induced eosinophil TBM and lower concentrations of LPS augmented neutrophil-induced eosinophil TBM. These results suggest that the combination of neutrophils and LPS leads eosinophils to accumulate in the airways, possibly involved the pathogenesis of severe asthma.<br />Competing Interests: Conflicts of Interest: None declared.

Details

Language :
English
ISSN :
2312-0541
Volume :
1
Issue :
2
Database :
MEDLINE
Journal :
ERJ open research
Publication Type :
Academic Journal
Accession number :
27730145
Full Text :
https://doi.org/10.1183/23120541.00003-2015