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IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake
Interleukin-22 (IL-22) acts protectively and harmfully on intestinal tissue depending on the situation; therefore, IL-22 signaling needs to be tightly regulated. IL-22 binding protein (IL-22BP) binds IL-22 to inhibit IL-22 signaling. It is expressed in intestinal and lymphoid tissues, although its p...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460992/ https://www.ncbi.nlm.nih.gov/pubmed/28512157 http://dx.doi.org/10.1084/jem.20160770 |
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author | Jinnohara, Toshi Kanaya, Takashi Hase, Koji Sakakibara, Sayuri Kato, Tamotsu Tachibana, Naoko Sasaki, Takaharu Hashimoto, Yusuke Sato, Toshiro Watarai, Hiroshi Kunisawa, Jun Shibata, Naoko Williams, Ifor R. Kiyono, Hiroshi Ohno, Hiroshi |
author_facet | Jinnohara, Toshi Kanaya, Takashi Hase, Koji Sakakibara, Sayuri Kato, Tamotsu Tachibana, Naoko Sasaki, Takaharu Hashimoto, Yusuke Sato, Toshiro Watarai, Hiroshi Kunisawa, Jun Shibata, Naoko Williams, Ifor R. Kiyono, Hiroshi Ohno, Hiroshi |
author_sort | Jinnohara, Toshi |
collection | PubMed |
description | Interleukin-22 (IL-22) acts protectively and harmfully on intestinal tissue depending on the situation; therefore, IL-22 signaling needs to be tightly regulated. IL-22 binding protein (IL-22BP) binds IL-22 to inhibit IL-22 signaling. It is expressed in intestinal and lymphoid tissues, although its precise distribution and roles have remained unclear. In this study, we show that IL-22BP is highly expressed by CD11b(+)CD8α(−) dendritic cells in the subepithelial dome region of Peyer’s patches (PPs). We found that IL-22BP blocks IL-22 signaling in the follicle-associated epithelium (FAE) covering PPs, indicating that IL-22BP plays a role in regulating the characteristics of the FAE. As expected, FAE of IL-22BP–deficient (Il22ra2(−)(/−)) mice exhibited altered properties such as the enhanced expression of mucus and antimicrobial proteins as well as prominent fucosylation, which are normally suppressed in FAE. Additionally, Il22ra2(−)(/−) mice exhibited the decreased uptake of bacterial antigens into PPs without affecting M cell function. Our present study thus demonstrates that IL-22BP promotes bacterial uptake into PPs by influencing FAE gene expression and function. |
format | Online Article Text |
id | pubmed-5460992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54609922017-12-05 IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake Jinnohara, Toshi Kanaya, Takashi Hase, Koji Sakakibara, Sayuri Kato, Tamotsu Tachibana, Naoko Sasaki, Takaharu Hashimoto, Yusuke Sato, Toshiro Watarai, Hiroshi Kunisawa, Jun Shibata, Naoko Williams, Ifor R. Kiyono, Hiroshi Ohno, Hiroshi J Exp Med Research Articles Interleukin-22 (IL-22) acts protectively and harmfully on intestinal tissue depending on the situation; therefore, IL-22 signaling needs to be tightly regulated. IL-22 binding protein (IL-22BP) binds IL-22 to inhibit IL-22 signaling. It is expressed in intestinal and lymphoid tissues, although its precise distribution and roles have remained unclear. In this study, we show that IL-22BP is highly expressed by CD11b(+)CD8α(−) dendritic cells in the subepithelial dome region of Peyer’s patches (PPs). We found that IL-22BP blocks IL-22 signaling in the follicle-associated epithelium (FAE) covering PPs, indicating that IL-22BP plays a role in regulating the characteristics of the FAE. As expected, FAE of IL-22BP–deficient (Il22ra2(−)(/−)) mice exhibited altered properties such as the enhanced expression of mucus and antimicrobial proteins as well as prominent fucosylation, which are normally suppressed in FAE. Additionally, Il22ra2(−)(/−) mice exhibited the decreased uptake of bacterial antigens into PPs without affecting M cell function. Our present study thus demonstrates that IL-22BP promotes bacterial uptake into PPs by influencing FAE gene expression and function. The Rockefeller University Press 2017-06-05 /pmc/articles/PMC5460992/ /pubmed/28512157 http://dx.doi.org/10.1084/jem.20160770 Text en © 2017 Jinnohara et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/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 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Jinnohara, Toshi Kanaya, Takashi Hase, Koji Sakakibara, Sayuri Kato, Tamotsu Tachibana, Naoko Sasaki, Takaharu Hashimoto, Yusuke Sato, Toshiro Watarai, Hiroshi Kunisawa, Jun Shibata, Naoko Williams, Ifor R. Kiyono, Hiroshi Ohno, Hiroshi IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake |
title | IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake |
title_full | IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake |
title_fullStr | IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake |
title_full_unstemmed | IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake |
title_short | IL-22BP dictates characteristics of Peyer’s patch follicle-associated epithelium for antigen uptake |
title_sort | il-22bp dictates characteristics of peyer’s patch follicle-associated epithelium for antigen uptake |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460992/ https://www.ncbi.nlm.nih.gov/pubmed/28512157 http://dx.doi.org/10.1084/jem.20160770 |
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