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

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 neu...

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Autores principales: Nishihara, Fuyumi, Nakagome, Kazuyuki, Kobayashi, Takehito, Noguchi, Toru, Araki, Ryuichiro, Uchida, Yoshitaka, Soma, Tomoyuki, Nagata, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005110/
https://www.ncbi.nlm.nih.gov/pubmed/27730145
http://dx.doi.org/10.1183/23120541.00003-2015
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author Nishihara, Fuyumi
Nakagome, Kazuyuki
Kobayashi, Takehito
Noguchi, Toru
Araki, Ryuichiro
Uchida, Yoshitaka
Soma, Tomoyuki
Nagata, Makoto
author_facet Nishihara, Fuyumi
Nakagome, Kazuyuki
Kobayashi, Takehito
Noguchi, Toru
Araki, Ryuichiro
Uchida, Yoshitaka
Soma, Tomoyuki
Nagata, Makoto
author_sort Nishihara, Fuyumi
collection PubMed
description 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(4) 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.
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spelling pubmed-50051102016-10-11 Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro Nishihara, Fuyumi Nakagome, Kazuyuki Kobayashi, Takehito Noguchi, Toru Araki, Ryuichiro Uchida, Yoshitaka Soma, Tomoyuki Nagata, Makoto ERJ Open Res Original Articles 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(4) 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. European Respiratory Society 2015-12-22 /pmc/articles/PMC5005110/ /pubmed/27730145 http://dx.doi.org/10.1183/23120541.00003-2015 Text en Copyright ©ERS 2015 http://creativecommons.org/licenses/by-nc/4.0/ This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0
spellingShingle Original Articles
Nishihara, Fuyumi
Nakagome, Kazuyuki
Kobayashi, Takehito
Noguchi, Toru
Araki, Ryuichiro
Uchida, Yoshitaka
Soma, Tomoyuki
Nagata, Makoto
Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro
title Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro
title_full Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro
title_fullStr Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro
title_full_unstemmed Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro
title_short Trans-basement membrane migration of eosinophils induced by LPS-stimulated neutrophils from human peripheral blood in vitro
title_sort trans-basement membrane migration of eosinophils induced by lps-stimulated neutrophils from human peripheral blood in vitro
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005110/
https://www.ncbi.nlm.nih.gov/pubmed/27730145
http://dx.doi.org/10.1183/23120541.00003-2015
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