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Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma

Although several studies have demonstrated that mesenchymal stem cells derived from adipose tissue (ASCs) can ameliorate allergic airway inflammation, the immunomodulatory mechanism of ASCs remains unclear. In this study, we investigated whether regulatory T cells (Tregs) induction is a potential me...

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Autores principales: Cho, Kyu-Sup, Park, Mi-Kyung, Kang, Shin-Ae, Park, Hee-Young, Hong, Sung-Lyong, Park, Hye-Kyung, Yu, Hak-Sun, Roh, Hwan-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160627/
https://www.ncbi.nlm.nih.gov/pubmed/25246732
http://dx.doi.org/10.1155/2014/436476
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author Cho, Kyu-Sup
Park, Mi-Kyung
Kang, Shin-Ae
Park, Hee-Young
Hong, Sung-Lyong
Park, Hye-Kyung
Yu, Hak-Sun
Roh, Hwan-Jung
author_facet Cho, Kyu-Sup
Park, Mi-Kyung
Kang, Shin-Ae
Park, Hee-Young
Hong, Sung-Lyong
Park, Hye-Kyung
Yu, Hak-Sun
Roh, Hwan-Jung
author_sort Cho, Kyu-Sup
collection PubMed
description Although several studies have demonstrated that mesenchymal stem cells derived from adipose tissue (ASCs) can ameliorate allergic airway inflammation, the immunomodulatory mechanism of ASCs remains unclear. In this study, we investigated whether regulatory T cells (Tregs) induction is a potential mechanism in immunomodulatory effects of ASCs on allergic airway disease and how these induced Tregs orchestrate allergic inflammation. Intravenous administration of ASCs significantly reduced allergic symptoms and inhibited eosinophilic inflammation. Airway hyperresponsiveness, total immune cell and eosinophils in the bronchoalveolar lavage fluid, mucus production, and serum allergen-specific IgE and IgG1 were significantly reduced after ASCs administration. ASCs significantly inhibited Th2 cytokines (IL-4, IL-5, and IL-13) and enhanced Th1 cytokine (IFN-γ) and regulatory cytokines (IL-10 and TGF-β) in the bronchoalveolar lavage fluid and lung draining lymph nodes. Furthermore, levels of IDO, TGF-β, and PGE(2) were significantly increased after ASCs administration. Interestingly, this upregulation was accompanied by increased Treg populations. In conclusion, ASCs ameliorated allergic airway inflammation and improved lung function through the induction of Treg expansion. The induction of Treg by ASCs involves the secretion of soluble factors such as IDO, TGF-β, and PGE(2) and Treg might be involved in the downregulation of Th2 cytokines and upregulation of Th1 cytokines production.
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spelling pubmed-41606272014-09-22 Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma Cho, Kyu-Sup Park, Mi-Kyung Kang, Shin-Ae Park, Hee-Young Hong, Sung-Lyong Park, Hye-Kyung Yu, Hak-Sun Roh, Hwan-Jung Mediators Inflamm Research Article Although several studies have demonstrated that mesenchymal stem cells derived from adipose tissue (ASCs) can ameliorate allergic airway inflammation, the immunomodulatory mechanism of ASCs remains unclear. In this study, we investigated whether regulatory T cells (Tregs) induction is a potential mechanism in immunomodulatory effects of ASCs on allergic airway disease and how these induced Tregs orchestrate allergic inflammation. Intravenous administration of ASCs significantly reduced allergic symptoms and inhibited eosinophilic inflammation. Airway hyperresponsiveness, total immune cell and eosinophils in the bronchoalveolar lavage fluid, mucus production, and serum allergen-specific IgE and IgG1 were significantly reduced after ASCs administration. ASCs significantly inhibited Th2 cytokines (IL-4, IL-5, and IL-13) and enhanced Th1 cytokine (IFN-γ) and regulatory cytokines (IL-10 and TGF-β) in the bronchoalveolar lavage fluid and lung draining lymph nodes. Furthermore, levels of IDO, TGF-β, and PGE(2) were significantly increased after ASCs administration. Interestingly, this upregulation was accompanied by increased Treg populations. In conclusion, ASCs ameliorated allergic airway inflammation and improved lung function through the induction of Treg expansion. The induction of Treg by ASCs involves the secretion of soluble factors such as IDO, TGF-β, and PGE(2) and Treg might be involved in the downregulation of Th2 cytokines and upregulation of Th1 cytokines production. Hindawi Publishing Corporation 2014 2014-08-26 /pmc/articles/PMC4160627/ /pubmed/25246732 http://dx.doi.org/10.1155/2014/436476 Text en Copyright © 2014 Kyu-Sup Cho et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cho, Kyu-Sup
Park, Mi-Kyung
Kang, Shin-Ae
Park, Hee-Young
Hong, Sung-Lyong
Park, Hye-Kyung
Yu, Hak-Sun
Roh, Hwan-Jung
Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma
title Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma
title_full Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma
title_fullStr Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma
title_full_unstemmed Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma
title_short Adipose-Derived Stem Cells Ameliorate Allergic Airway Inflammation by Inducing Regulatory T Cells in a Mouse Model of Asthma
title_sort adipose-derived stem cells ameliorate allergic airway inflammation by inducing regulatory t cells in a mouse model of asthma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160627/
https://www.ncbi.nlm.nih.gov/pubmed/25246732
http://dx.doi.org/10.1155/2014/436476
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