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The Role of TSLP in IL-13-Induced Atopic March
Although atopic dermatitis (AD) is the initial step of the “atopic march”, a progression from AD to asthma, the underlying mechanism remains unknown. Selective expression of IL-13 in the skin of mice caused an AD phenotype resembling human AD, and the disorder was associated with enhanced production...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251897/ https://www.ncbi.nlm.nih.gov/pubmed/22355542 http://dx.doi.org/10.1038/srep00023 |
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author | Zhu, Zhou Oh, Min-Hee Yu, Jinho Liu, Yong Jun Zheng, Tao |
author_facet | Zhu, Zhou Oh, Min-Hee Yu, Jinho Liu, Yong Jun Zheng, Tao |
author_sort | Zhu, Zhou |
collection | PubMed |
description | Although atopic dermatitis (AD) is the initial step of the “atopic march”, a progression from AD to asthma, the underlying mechanism remains unknown. Selective expression of IL-13 in the skin of mice caused an AD phenotype resembling human AD, and the disorder was associated with enhanced production of thymic stromal lymphopoietin (TSLP) in the AD skin with a systemic Th2 immunity. Here we show that IL-13 transgenic mice with AD had significantly enhanced lung inflammation, mucus hypersecretion, and airway hyperresponsiveness (AHR) when sensitized and challenged by allergen. In addition, the level of TSLP was significantly higher in acute AD than in chronic AD. Furthermore, elimination of TSLP signaling significantly diminished the allergic asthma responses, immune cell production of Th2 cytokines (IL-4, IL-13), and serum IgE. These studies indicate that IL-13 induces AD and atopic march via a TSLP dependent mechanism. |
format | Online Article Text |
id | pubmed-3251897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32518972012-01-10 The Role of TSLP in IL-13-Induced Atopic March Zhu, Zhou Oh, Min-Hee Yu, Jinho Liu, Yong Jun Zheng, Tao Sci Rep Article Although atopic dermatitis (AD) is the initial step of the “atopic march”, a progression from AD to asthma, the underlying mechanism remains unknown. Selective expression of IL-13 in the skin of mice caused an AD phenotype resembling human AD, and the disorder was associated with enhanced production of thymic stromal lymphopoietin (TSLP) in the AD skin with a systemic Th2 immunity. Here we show that IL-13 transgenic mice with AD had significantly enhanced lung inflammation, mucus hypersecretion, and airway hyperresponsiveness (AHR) when sensitized and challenged by allergen. In addition, the level of TSLP was significantly higher in acute AD than in chronic AD. Furthermore, elimination of TSLP signaling significantly diminished the allergic asthma responses, immune cell production of Th2 cytokines (IL-4, IL-13), and serum IgE. These studies indicate that IL-13 induces AD and atopic march via a TSLP dependent mechanism. Nature Publishing Group 2011-07-15 /pmc/articles/PMC3251897/ /pubmed/22355542 http://dx.doi.org/10.1038/srep00023 Text en Copyright © 2011, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Zhu, Zhou Oh, Min-Hee Yu, Jinho Liu, Yong Jun Zheng, Tao The Role of TSLP in IL-13-Induced Atopic March |
title | The Role of TSLP in IL-13-Induced Atopic March |
title_full | The Role of TSLP in IL-13-Induced Atopic March |
title_fullStr | The Role of TSLP in IL-13-Induced Atopic March |
title_full_unstemmed | The Role of TSLP in IL-13-Induced Atopic March |
title_short | The Role of TSLP in IL-13-Induced Atopic March |
title_sort | role of tslp in il-13-induced atopic march |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251897/ https://www.ncbi.nlm.nih.gov/pubmed/22355542 http://dx.doi.org/10.1038/srep00023 |
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