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CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production
Eosinophils and their associated cytokines IL-4 and IL-5 are emerging as central orchestrators of the immune-metabolic axis. Herein, we demonstrate that cross-talk between the Ig-superfamily receptor CD300f and IL-5 is a key checkpoint that modifies the ability of eosinophils to regulate metabolic o...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517555/ https://www.ncbi.nlm.nih.gov/pubmed/28725048 http://dx.doi.org/10.1038/s41598-017-06397-4 |
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author | Rozenberg, Perri Reichman, Hadar Zab-Bar, Israel Itan, Michal Pasmanik-Chor, Metsada Bouffi, Carine Qimron, Udi Bachelet, Ido Fulkerson, Patricia C. Rothenberg, Marc E. Munitz, Ariel |
author_facet | Rozenberg, Perri Reichman, Hadar Zab-Bar, Israel Itan, Michal Pasmanik-Chor, Metsada Bouffi, Carine Qimron, Udi Bachelet, Ido Fulkerson, Patricia C. Rothenberg, Marc E. Munitz, Ariel |
author_sort | Rozenberg, Perri |
collection | PubMed |
description | Eosinophils and their associated cytokines IL-4 and IL-5 are emerging as central orchestrators of the immune-metabolic axis. Herein, we demonstrate that cross-talk between the Ig-superfamily receptor CD300f and IL-5 is a key checkpoint that modifies the ability of eosinophils to regulate metabolic outcomes. Generation of Il5 (Tg) /Cd300f (−/−) mice revealed marked and distinct increases in eosinophil levels and their production of IL-4 in the white and brown adipose tissues. Consequently, Il5 (Tg) /Cd300f (−/−) mice had increased alternatively activated macrophage accumulation in the adipose tissue. Cd300f (−/−) mice displayed age-related accumulation of eosinophils and macrophages in the adipose tissue and decreased adipose tissue weight, which was associated with decreased diet-induced weight gain and insulin resistance. Notably, Il5 (Tg) /CD300f (−/−) were protected from diet-induced weight gain and glucose intolerance. These findings highlight the cross-talk between IL-5 receptor and CD300f as a novel pathway regulating adipose tissue eosinophils and offer new entry points for therapeutic intervention for obesity and its complications. |
format | Online Article Text |
id | pubmed-5517555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55175552017-07-20 CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production Rozenberg, Perri Reichman, Hadar Zab-Bar, Israel Itan, Michal Pasmanik-Chor, Metsada Bouffi, Carine Qimron, Udi Bachelet, Ido Fulkerson, Patricia C. Rothenberg, Marc E. Munitz, Ariel Sci Rep Article Eosinophils and their associated cytokines IL-4 and IL-5 are emerging as central orchestrators of the immune-metabolic axis. Herein, we demonstrate that cross-talk between the Ig-superfamily receptor CD300f and IL-5 is a key checkpoint that modifies the ability of eosinophils to regulate metabolic outcomes. Generation of Il5 (Tg) /Cd300f (−/−) mice revealed marked and distinct increases in eosinophil levels and their production of IL-4 in the white and brown adipose tissues. Consequently, Il5 (Tg) /Cd300f (−/−) mice had increased alternatively activated macrophage accumulation in the adipose tissue. Cd300f (−/−) mice displayed age-related accumulation of eosinophils and macrophages in the adipose tissue and decreased adipose tissue weight, which was associated with decreased diet-induced weight gain and insulin resistance. Notably, Il5 (Tg) /CD300f (−/−) were protected from diet-induced weight gain and glucose intolerance. These findings highlight the cross-talk between IL-5 receptor and CD300f as a novel pathway regulating adipose tissue eosinophils and offer new entry points for therapeutic intervention for obesity and its complications. Nature Publishing Group UK 2017-07-19 /pmc/articles/PMC5517555/ /pubmed/28725048 http://dx.doi.org/10.1038/s41598-017-06397-4 Text en © The Author(s) 2017 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 Rozenberg, Perri Reichman, Hadar Zab-Bar, Israel Itan, Michal Pasmanik-Chor, Metsada Bouffi, Carine Qimron, Udi Bachelet, Ido Fulkerson, Patricia C. Rothenberg, Marc E. Munitz, Ariel CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production |
title | CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production |
title_full | CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production |
title_fullStr | CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production |
title_full_unstemmed | CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production |
title_short | CD300f:IL-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent IL-4 production |
title_sort | cd300f:il-5 cross-talk inhibits adipose tissue eosinophil homing and subsequent il-4 production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517555/ https://www.ncbi.nlm.nih.gov/pubmed/28725048 http://dx.doi.org/10.1038/s41598-017-06397-4 |
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