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AHR and the Transcriptional Regulation of Type-17/22 ILC
Mucosal innate lymphoid cells (ILCs) are an emerging population of diverse and heterogeneous immune cells, all with the unique ability to mount a rapid response against invading pathogens. They are further divided into subsets based on their differing cell surface markers as well as in their functio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342302/ https://www.ncbi.nlm.nih.gov/pubmed/22566896 http://dx.doi.org/10.3389/fimmu.2012.00010 |
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author | Lee, Jacob S. Cella, Marina Colonna, Marco |
author_facet | Lee, Jacob S. Cella, Marina Colonna, Marco |
author_sort | Lee, Jacob S. |
collection | PubMed |
description | Mucosal innate lymphoid cells (ILCs) are an emerging population of diverse and heterogeneous immune cells, all with the unique ability to mount a rapid response against invading pathogens. They are further divided into subsets based on their differing cell surface markers as well as in their functional specialization. In this review, we summarize recent reports describing the importance of the transcription factor aryl hydrocarbon receptor (AHR) in regulating the development of one of these subsets, the Type-17/22 ILCs, as well as in the organization of postnatal lymphoid structures. We discuss the mechanisms behind the AHR dependence for development in Type-17/22 ILCs as well as reviewing the proposed physiological ligands that are mediating this effect. |
format | Online Article Text |
id | pubmed-3342302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33423022012-05-07 AHR and the Transcriptional Regulation of Type-17/22 ILC Lee, Jacob S. Cella, Marina Colonna, Marco Front Immunol Immunology Mucosal innate lymphoid cells (ILCs) are an emerging population of diverse and heterogeneous immune cells, all with the unique ability to mount a rapid response against invading pathogens. They are further divided into subsets based on their differing cell surface markers as well as in their functional specialization. In this review, we summarize recent reports describing the importance of the transcription factor aryl hydrocarbon receptor (AHR) in regulating the development of one of these subsets, the Type-17/22 ILCs, as well as in the organization of postnatal lymphoid structures. We discuss the mechanisms behind the AHR dependence for development in Type-17/22 ILCs as well as reviewing the proposed physiological ligands that are mediating this effect. Frontiers Research Foundation 2012-02-06 /pmc/articles/PMC3342302/ /pubmed/22566896 http://dx.doi.org/10.3389/fimmu.2012.00010 Text en Copyright © 2012 Lee, Cella and Colonna. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Immunology Lee, Jacob S. Cella, Marina Colonna, Marco AHR and the Transcriptional Regulation of Type-17/22 ILC |
title | AHR and the Transcriptional Regulation of Type-17/22 ILC |
title_full | AHR and the Transcriptional Regulation of Type-17/22 ILC |
title_fullStr | AHR and the Transcriptional Regulation of Type-17/22 ILC |
title_full_unstemmed | AHR and the Transcriptional Regulation of Type-17/22 ILC |
title_short | AHR and the Transcriptional Regulation of Type-17/22 ILC |
title_sort | ahr and the transcriptional regulation of type-17/22 ilc |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342302/ https://www.ncbi.nlm.nih.gov/pubmed/22566896 http://dx.doi.org/10.3389/fimmu.2012.00010 |
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