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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...

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Detalles Bibliográficos
Autores principales: Lee, Jacob S., Cella, Marina, Colonna, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
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.
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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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