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Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice

Eosinophil degranulation is a determining factor in allergy-mediated airway pathology. Receptor-mediated degranulation in eosinophils requires vesicle-associated membrane protein 7 (VAMP-7), a principal component of the SNARE fusion machinery. The specific contribution of eosinophil degranulation to...

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Autores principales: Willetts, Lian, Felix, Lindsey C., Jacobsen, Elizabeth A., Puttagunta, Lakshmi, Condjella, Rachel M., Zellner, Katie R., Ochkur, Sergei I., Kim, John D., Luo, Huijun, Lee, Nancy A., Lee, James J., Moqbel, Redwan, Lacy, Paige
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123774/
https://www.ncbi.nlm.nih.gov/pubmed/30271964
http://dx.doi.org/10.1038/s42003-018-0081-z
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author Willetts, Lian
Felix, Lindsey C.
Jacobsen, Elizabeth A.
Puttagunta, Lakshmi
Condjella, Rachel M.
Zellner, Katie R.
Ochkur, Sergei I.
Kim, John D.
Luo, Huijun
Lee, Nancy A.
Lee, James J.
Moqbel, Redwan
Lacy, Paige
author_facet Willetts, Lian
Felix, Lindsey C.
Jacobsen, Elizabeth A.
Puttagunta, Lakshmi
Condjella, Rachel M.
Zellner, Katie R.
Ochkur, Sergei I.
Kim, John D.
Luo, Huijun
Lee, Nancy A.
Lee, James J.
Moqbel, Redwan
Lacy, Paige
author_sort Willetts, Lian
collection PubMed
description Eosinophil degranulation is a determining factor in allergy-mediated airway pathology. Receptor-mediated degranulation in eosinophils requires vesicle-associated membrane protein 7 (VAMP-7), a principal component of the SNARE fusion machinery. The specific contribution of eosinophil degranulation to allergen-induced airway responses remains poorly understood. We generated mice with VAMP-7 gene deficiency exclusively in eosinophils (eoCRE/V7) from a cross using eosinophil-specific Cre recombinase-expressing mice crossed with VAMP-7(f/f) mice. Eosinophils from eoCRE/V7 mice showed deficient degranulation responses in vitro, and responses continued to be decreased following ex vivo intratracheal adoptive transfer of eoCRE/V7 eosinophils into IL-5/hE2/EPX(−/−) mice. Consistent with diminished degranulation responses, reduced airway hyperresponsiveness was observed in ovalbumin-sensitized and challenged eoCRE/V7 mice following methacholine inhalation. Therefore, VAMP-7 mediates eosinophil degranulation both in vitro and ex vivo, and this event augments airway hyperresponsiveness.
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spelling pubmed-61237742018-09-28 Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice Willetts, Lian Felix, Lindsey C. Jacobsen, Elizabeth A. Puttagunta, Lakshmi Condjella, Rachel M. Zellner, Katie R. Ochkur, Sergei I. Kim, John D. Luo, Huijun Lee, Nancy A. Lee, James J. Moqbel, Redwan Lacy, Paige Commun Biol Article Eosinophil degranulation is a determining factor in allergy-mediated airway pathology. Receptor-mediated degranulation in eosinophils requires vesicle-associated membrane protein 7 (VAMP-7), a principal component of the SNARE fusion machinery. The specific contribution of eosinophil degranulation to allergen-induced airway responses remains poorly understood. We generated mice with VAMP-7 gene deficiency exclusively in eosinophils (eoCRE/V7) from a cross using eosinophil-specific Cre recombinase-expressing mice crossed with VAMP-7(f/f) mice. Eosinophils from eoCRE/V7 mice showed deficient degranulation responses in vitro, and responses continued to be decreased following ex vivo intratracheal adoptive transfer of eoCRE/V7 eosinophils into IL-5/hE2/EPX(−/−) mice. Consistent with diminished degranulation responses, reduced airway hyperresponsiveness was observed in ovalbumin-sensitized and challenged eoCRE/V7 mice following methacholine inhalation. Therefore, VAMP-7 mediates eosinophil degranulation both in vitro and ex vivo, and this event augments airway hyperresponsiveness. Nature Publishing Group UK 2018-06-29 /pmc/articles/PMC6123774/ /pubmed/30271964 http://dx.doi.org/10.1038/s42003-018-0081-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Willetts, Lian
Felix, Lindsey C.
Jacobsen, Elizabeth A.
Puttagunta, Lakshmi
Condjella, Rachel M.
Zellner, Katie R.
Ochkur, Sergei I.
Kim, John D.
Luo, Huijun
Lee, Nancy A.
Lee, James J.
Moqbel, Redwan
Lacy, Paige
Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
title Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
title_full Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
title_fullStr Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
title_full_unstemmed Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
title_short Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
title_sort vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123774/
https://www.ncbi.nlm.nih.gov/pubmed/30271964
http://dx.doi.org/10.1038/s42003-018-0081-z
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