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Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function
Epithelial cells orchestrate pulmonary homeostasis and pathogen defense and play a crucial role in the initiation of allergic immune responses. Maintaining the balance between homeostasis and inappropriate immune activation and associated pathology is particularly complex at mucosal sites that are e...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658339/ https://www.ncbi.nlm.nih.gov/pubmed/26588780 http://dx.doi.org/10.1016/j.immuni.2015.10.012 |
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author | Denney, Laura Byrne, Adam J. Shea, Thomas J. Buckley, James S. Pease, James E. Herledan, Gaelle M.F. Walker, Simone A. Gregory, Lisa G. Lloyd, Clare M. |
author_facet | Denney, Laura Byrne, Adam J. Shea, Thomas J. Buckley, James S. Pease, James E. Herledan, Gaelle M.F. Walker, Simone A. Gregory, Lisa G. Lloyd, Clare M. |
author_sort | Denney, Laura |
collection | PubMed |
description | Epithelial cells orchestrate pulmonary homeostasis and pathogen defense and play a crucial role in the initiation of allergic immune responses. Maintaining the balance between homeostasis and inappropriate immune activation and associated pathology is particularly complex at mucosal sites that are exposed to billions of potentially antigenic particles daily. We demonstrated that epithelial cell-derived cytokine TGF-β had a central role in the generation of the pulmonary immune response. Mice that specifically lacked epithelial cell-derived TGF-β1 displayed a reduction in type 2 innate lymphoid cells (ILCs), resulting in suppression of interleukin-13 and hallmark features of the allergic response including airway hyperreactivity. ILCs in the airway lumen were primed to respond to TGF-β by expressing the receptor TGF-βRII and ILC chemoactivity was enhanced by TGF-β. These data demonstrate that resident epithelial cells instruct immune cells, highlighting the central role of the local environmental niche in defining the nature and magnitude of immune reactions. |
format | Online Article Text |
id | pubmed-4658339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46583392016-01-11 Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function Denney, Laura Byrne, Adam J. Shea, Thomas J. Buckley, James S. Pease, James E. Herledan, Gaelle M.F. Walker, Simone A. Gregory, Lisa G. Lloyd, Clare M. Immunity Article Epithelial cells orchestrate pulmonary homeostasis and pathogen defense and play a crucial role in the initiation of allergic immune responses. Maintaining the balance between homeostasis and inappropriate immune activation and associated pathology is particularly complex at mucosal sites that are exposed to billions of potentially antigenic particles daily. We demonstrated that epithelial cell-derived cytokine TGF-β had a central role in the generation of the pulmonary immune response. Mice that specifically lacked epithelial cell-derived TGF-β1 displayed a reduction in type 2 innate lymphoid cells (ILCs), resulting in suppression of interleukin-13 and hallmark features of the allergic response including airway hyperreactivity. ILCs in the airway lumen were primed to respond to TGF-β by expressing the receptor TGF-βRII and ILC chemoactivity was enhanced by TGF-β. These data demonstrate that resident epithelial cells instruct immune cells, highlighting the central role of the local environmental niche in defining the nature and magnitude of immune reactions. Cell Press 2015-11-17 /pmc/articles/PMC4658339/ /pubmed/26588780 http://dx.doi.org/10.1016/j.immuni.2015.10.012 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Denney, Laura Byrne, Adam J. Shea, Thomas J. Buckley, James S. Pease, James E. Herledan, Gaelle M.F. Walker, Simone A. Gregory, Lisa G. Lloyd, Clare M. Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function |
title | Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function |
title_full | Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function |
title_fullStr | Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function |
title_full_unstemmed | Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function |
title_short | Pulmonary Epithelial Cell-Derived Cytokine TGF-β1 Is a Critical Cofactor for Enhanced Innate Lymphoid Cell Function |
title_sort | pulmonary epithelial cell-derived cytokine tgf-β1 is a critical cofactor for enhanced innate lymphoid cell function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658339/ https://www.ncbi.nlm.nih.gov/pubmed/26588780 http://dx.doi.org/10.1016/j.immuni.2015.10.012 |
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