Hypoxia modulates human eosinophil function

<p>Abstract</p> <p>Background</p> <p>Eosinophils are involved in various inflammatory processes including allergic inflammation during which angiogenesis has been documented. Angiogenesis is most likely connected to the hypoxia which characterizes inflamed tissues. Eosi...

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Main Authors: Levi-Schaffer Francesca, Eliashar Ron, Nissim Ben Efraim Alon H
Format: Article
Language:English
Published: BMC 2010-07-01
Series:Clinical and Molecular Allergy
Online Access:http://www.clinicalmolecularallergy.com/content/8/1/10
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spelling doaj-626da143d53f45c4b42e74ea3d9820272020-11-24T22:24:48ZengBMCClinical and Molecular Allergy1476-79612010-07-01811010.1186/1476-7961-8-10Hypoxia modulates human eosinophil functionLevi-Schaffer FrancescaEliashar RonNissim Ben Efraim Alon H<p>Abstract</p> <p>Background</p> <p>Eosinophils are involved in various inflammatory processes including allergic inflammation during which angiogenesis has been documented. Angiogenesis is most likely connected to the hypoxia which characterizes inflamed tissues. Eosinophils produce VEGF and are pro-angiogenic. However, to the best of our knowledge no study has been performed to verify the existence of a direct link between eosinophils, hypoxia and angiogenesis in allergic inflammation.</p> <p>Objective</p> <p>To characterize eosinophil function and angiogenic potential under hypoxic conditions.</p> <p>Methods</p> <p>Human peripheral blood eosinophils were cultured in normoxic or hypoxic conditions with or without cytokines. Viability and apoptosis were assessed by Annexin V/PI staining. Anti- or pro-apoptotic protein levels, HIF-1α levels and MAPK phosphorylation were analyzed by immunoblot analysis. Angiogenic mediator release was evaluated by ELISA.</p> <p>Results</p> <p>Hypoxic eosinophils were more viable than normoxic ones after up to three days. In addition in hypoxia, anti-apoptotic Bcl-XL protein levels increased more than pro-apoptotic Bax levels. Hypoxia increased VEGF and IL-8 release. In hypoxic eosinophils high levels of HIF-1α were observed, particularly in the presence of GM-CSF. MAPK, particularly ERK1/2 inhibitors, decreased hypoxia-mediated VEGF release and HIF-1α expression.</p> <p>Conclusion</p> <p>Eosinophils respond to hypoxia by up-regulation of survival and of some of their pro-angiogenic functions indicating a correlation between eosinophilic inflammation and angiogenesis.</p> http://www.clinicalmolecularallergy.com/content/8/1/10
collection DOAJ
language English
format Article
sources DOAJ
author Levi-Schaffer Francesca
Eliashar Ron
Nissim Ben Efraim Alon H
spellingShingle Levi-Schaffer Francesca
Eliashar Ron
Nissim Ben Efraim Alon H
Hypoxia modulates human eosinophil function
Clinical and Molecular Allergy
author_facet Levi-Schaffer Francesca
Eliashar Ron
Nissim Ben Efraim Alon H
author_sort Levi-Schaffer Francesca
title Hypoxia modulates human eosinophil function
title_short Hypoxia modulates human eosinophil function
title_full Hypoxia modulates human eosinophil function
title_fullStr Hypoxia modulates human eosinophil function
title_full_unstemmed Hypoxia modulates human eosinophil function
title_sort hypoxia modulates human eosinophil function
publisher BMC
series Clinical and Molecular Allergy
issn 1476-7961
publishDate 2010-07-01
description <p>Abstract</p> <p>Background</p> <p>Eosinophils are involved in various inflammatory processes including allergic inflammation during which angiogenesis has been documented. Angiogenesis is most likely connected to the hypoxia which characterizes inflamed tissues. Eosinophils produce VEGF and are pro-angiogenic. However, to the best of our knowledge no study has been performed to verify the existence of a direct link between eosinophils, hypoxia and angiogenesis in allergic inflammation.</p> <p>Objective</p> <p>To characterize eosinophil function and angiogenic potential under hypoxic conditions.</p> <p>Methods</p> <p>Human peripheral blood eosinophils were cultured in normoxic or hypoxic conditions with or without cytokines. Viability and apoptosis were assessed by Annexin V/PI staining. Anti- or pro-apoptotic protein levels, HIF-1α levels and MAPK phosphorylation were analyzed by immunoblot analysis. Angiogenic mediator release was evaluated by ELISA.</p> <p>Results</p> <p>Hypoxic eosinophils were more viable than normoxic ones after up to three days. In addition in hypoxia, anti-apoptotic Bcl-XL protein levels increased more than pro-apoptotic Bax levels. Hypoxia increased VEGF and IL-8 release. In hypoxic eosinophils high levels of HIF-1α were observed, particularly in the presence of GM-CSF. MAPK, particularly ERK1/2 inhibitors, decreased hypoxia-mediated VEGF release and HIF-1α expression.</p> <p>Conclusion</p> <p>Eosinophils respond to hypoxia by up-regulation of survival and of some of their pro-angiogenic functions indicating a correlation between eosinophilic inflammation and angiogenesis.</p>
url http://www.clinicalmolecularallergy.com/content/8/1/10
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