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Eosinophils are key regulators of perivascular adipose tissue and vascular functionality
Obesity impairs the relaxant capacity of adipose tissue surrounding the vasculature (PVAT) and has been implicated in resultant obesity-related hypertension and impaired glucose intolerance. Resident immune cells are thought to regulate adipocyte activity. We investigated the role of eosinophils in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356000/ https://www.ncbi.nlm.nih.gov/pubmed/28303919 http://dx.doi.org/10.1038/srep44571 |
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author | Withers, Sarah B. Forman, Ruth Meza-Perez, Selene Sorobetea, Daniel Sitnik, Kasia Hopwood, Thomas Lawrence, Catherine B. Agace, William W. Else, Kathryn J. Heagerty, Anthony M. Svensson-Frej, Marcus Cruickshank, Sheena M. |
author_facet | Withers, Sarah B. Forman, Ruth Meza-Perez, Selene Sorobetea, Daniel Sitnik, Kasia Hopwood, Thomas Lawrence, Catherine B. Agace, William W. Else, Kathryn J. Heagerty, Anthony M. Svensson-Frej, Marcus Cruickshank, Sheena M. |
author_sort | Withers, Sarah B. |
collection | PubMed |
description | Obesity impairs the relaxant capacity of adipose tissue surrounding the vasculature (PVAT) and has been implicated in resultant obesity-related hypertension and impaired glucose intolerance. Resident immune cells are thought to regulate adipocyte activity. We investigated the role of eosinophils in mediating normal PVAT function. Healthy PVAT elicits an anti-contractile effect, which was lost in mice deficient in eosinophils, mimicking the obese phenotype, and was restored upon eosinophil reconstitution. Ex vivo studies demonstrated that the loss of PVAT function was due to reduced bioavailability of adiponectin and adipocyte-derived nitric oxide, which was restored after eosinophil reconstitution. Mechanistic studies demonstrated that adiponectin and nitric oxide are released after activation of adipocyte-expressed β3 adrenoceptors by catecholamines, and identified eosinophils as a novel source of these mediators. We conclude that adipose tissue eosinophils play a key role in the regulation of normal PVAT anti-contractile function. |
format | Online Article Text |
id | pubmed-5356000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53560002017-03-22 Eosinophils are key regulators of perivascular adipose tissue and vascular functionality Withers, Sarah B. Forman, Ruth Meza-Perez, Selene Sorobetea, Daniel Sitnik, Kasia Hopwood, Thomas Lawrence, Catherine B. Agace, William W. Else, Kathryn J. Heagerty, Anthony M. Svensson-Frej, Marcus Cruickshank, Sheena M. Sci Rep Article Obesity impairs the relaxant capacity of adipose tissue surrounding the vasculature (PVAT) and has been implicated in resultant obesity-related hypertension and impaired glucose intolerance. Resident immune cells are thought to regulate adipocyte activity. We investigated the role of eosinophils in mediating normal PVAT function. Healthy PVAT elicits an anti-contractile effect, which was lost in mice deficient in eosinophils, mimicking the obese phenotype, and was restored upon eosinophil reconstitution. Ex vivo studies demonstrated that the loss of PVAT function was due to reduced bioavailability of adiponectin and adipocyte-derived nitric oxide, which was restored after eosinophil reconstitution. Mechanistic studies demonstrated that adiponectin and nitric oxide are released after activation of adipocyte-expressed β3 adrenoceptors by catecholamines, and identified eosinophils as a novel source of these mediators. We conclude that adipose tissue eosinophils play a key role in the regulation of normal PVAT anti-contractile function. Nature Publishing Group 2017-03-17 /pmc/articles/PMC5356000/ /pubmed/28303919 http://dx.doi.org/10.1038/srep44571 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Withers, Sarah B. Forman, Ruth Meza-Perez, Selene Sorobetea, Daniel Sitnik, Kasia Hopwood, Thomas Lawrence, Catherine B. Agace, William W. Else, Kathryn J. Heagerty, Anthony M. Svensson-Frej, Marcus Cruickshank, Sheena M. Eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
title | Eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
title_full | Eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
title_fullStr | Eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
title_full_unstemmed | Eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
title_short | Eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
title_sort | eosinophils are key regulators of perivascular adipose tissue and vascular functionality |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356000/ https://www.ncbi.nlm.nih.gov/pubmed/28303919 http://dx.doi.org/10.1038/srep44571 |
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