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Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist
Eosinophils play proinflammatory roles in helminth infections and allergic diseases. Under steady-state conditions, eosinophils are abundantly found in the small intestinal lamina propria, but their physiological function is largely unexplored. In this study, we found that small intestinal eosinophi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821642/ https://www.ncbi.nlm.nih.gov/pubmed/26951334 http://dx.doi.org/10.1084/jem.20141388 |
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author | Sugawara, Reiko Lee, Eun-Jung Jang, Min Seong Jeun, Eun-Ji Hong, Chun-Pyo Kim, Jung-Hwan Park, Areum Yun, Chang Ho Hong, Sung-Wook Kim, You-Me Seoh, Ju-Young Jung, YunJae Surh, Charles D. Miyasaka, Masayuki Yang, Bo-Gie Jang, Myoung Ho |
author_facet | Sugawara, Reiko Lee, Eun-Jung Jang, Min Seong Jeun, Eun-Ji Hong, Chun-Pyo Kim, Jung-Hwan Park, Areum Yun, Chang Ho Hong, Sung-Wook Kim, You-Me Seoh, Ju-Young Jung, YunJae Surh, Charles D. Miyasaka, Masayuki Yang, Bo-Gie Jang, Myoung Ho |
author_sort | Sugawara, Reiko |
collection | PubMed |
description | Eosinophils play proinflammatory roles in helminth infections and allergic diseases. Under steady-state conditions, eosinophils are abundantly found in the small intestinal lamina propria, but their physiological function is largely unexplored. In this study, we found that small intestinal eosinophils down-regulate Th17 cells. Th17 cells in the small intestine were markedly increased in the ΔdblGATA-1 mice lacking eosinophils, and an inverse correlation was observed between the number of eosinophils and that of Th17 cells in the small intestine of wild-type mice. In addition, small intestinal eosinophils suppressed the in vitro differentiation of Th17 cells, as well as IL-17 production by small intestinal CD4(+) T cells. Unlike other small intestinal immune cells or circulating eosinophils, we found that small intestinal eosinophils have a unique ability to constitutively secrete high levels of IL-1 receptor antagonist (IL-1Ra), a natural inhibitor of IL-1β. Moreover, small intestinal eosinophils isolated from IL-1Ra−deficient mice failed to suppress Th17 cells. Collectively, our results demonstrate that small intestinal eosinophils play a pivotal role in the maintenance of intestinal homeostasis by regulating Th17 cells via production of IL-1Ra. |
format | Online Article Text |
id | pubmed-4821642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48216422016-10-04 Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist Sugawara, Reiko Lee, Eun-Jung Jang, Min Seong Jeun, Eun-Ji Hong, Chun-Pyo Kim, Jung-Hwan Park, Areum Yun, Chang Ho Hong, Sung-Wook Kim, You-Me Seoh, Ju-Young Jung, YunJae Surh, Charles D. Miyasaka, Masayuki Yang, Bo-Gie Jang, Myoung Ho J Exp Med Research Articles Eosinophils play proinflammatory roles in helminth infections and allergic diseases. Under steady-state conditions, eosinophils are abundantly found in the small intestinal lamina propria, but their physiological function is largely unexplored. In this study, we found that small intestinal eosinophils down-regulate Th17 cells. Th17 cells in the small intestine were markedly increased in the ΔdblGATA-1 mice lacking eosinophils, and an inverse correlation was observed between the number of eosinophils and that of Th17 cells in the small intestine of wild-type mice. In addition, small intestinal eosinophils suppressed the in vitro differentiation of Th17 cells, as well as IL-17 production by small intestinal CD4(+) T cells. Unlike other small intestinal immune cells or circulating eosinophils, we found that small intestinal eosinophils have a unique ability to constitutively secrete high levels of IL-1 receptor antagonist (IL-1Ra), a natural inhibitor of IL-1β. Moreover, small intestinal eosinophils isolated from IL-1Ra−deficient mice failed to suppress Th17 cells. Collectively, our results demonstrate that small intestinal eosinophils play a pivotal role in the maintenance of intestinal homeostasis by regulating Th17 cells via production of IL-1Ra. The Rockefeller University Press 2016-04-04 /pmc/articles/PMC4821642/ /pubmed/26951334 http://dx.doi.org/10.1084/jem.20141388 Text en © 2016 Sugawara et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Sugawara, Reiko Lee, Eun-Jung Jang, Min Seong Jeun, Eun-Ji Hong, Chun-Pyo Kim, Jung-Hwan Park, Areum Yun, Chang Ho Hong, Sung-Wook Kim, You-Me Seoh, Ju-Young Jung, YunJae Surh, Charles D. Miyasaka, Masayuki Yang, Bo-Gie Jang, Myoung Ho Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist |
title | Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist |
title_full | Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist |
title_fullStr | Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist |
title_full_unstemmed | Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist |
title_short | Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist |
title_sort | small intestinal eosinophils regulate th17 cells by producing il-1 receptor antagonist |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821642/ https://www.ncbi.nlm.nih.gov/pubmed/26951334 http://dx.doi.org/10.1084/jem.20141388 |
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