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Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection
Innate immune cells detect pathogens via pattern recognition receptors (PRRs), which signal for initiation of immune responses to infection. Studies with Dectin-1, a PRR for fungi, have defined a novel innate signaling pathway involving Syk kinase and the adaptor CARD9, which is critical for inducin...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737172/ https://www.ncbi.nlm.nih.gov/pubmed/19703985 http://dx.doi.org/10.1084/jem.20082818 |
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author | Robinson, Matthew J. Osorio, Fabiola Rosas, Marcela Freitas, Rui P. Schweighoffer, Edina Groß, Olaf Verbeek, J. Sjef Ruland, Jürgen Tybulewicz, Victor Brown, Gordon D. Moita, Luis Ferreira Taylor, Philip R. Reis e Sousa, Caetano |
author_facet | Robinson, Matthew J. Osorio, Fabiola Rosas, Marcela Freitas, Rui P. Schweighoffer, Edina Groß, Olaf Verbeek, J. Sjef Ruland, Jürgen Tybulewicz, Victor Brown, Gordon D. Moita, Luis Ferreira Taylor, Philip R. Reis e Sousa, Caetano |
author_sort | Robinson, Matthew J. |
collection | PubMed |
description | Innate immune cells detect pathogens via pattern recognition receptors (PRRs), which signal for initiation of immune responses to infection. Studies with Dectin-1, a PRR for fungi, have defined a novel innate signaling pathway involving Syk kinase and the adaptor CARD9, which is critical for inducing Th17 responses to fungal infection. We show that another C-type lectin, Dectin-2, also signals via Syk and CARD9, and contributes to dendritic cell (DC) activation by fungal particles. Unlike Dectin-1, Dectin-2 couples to Syk indirectly, through association with the FcRγ chain. In a model of Candida albicans infection, blockade of Dectin-2 did not affect innate immune resistance but abrogated Candida-specific T cell production of IL-17 and, in combination with the absence of Dectin-1, decreased Th1 responses to the organism. Thus, Dectin-2 constitutes a major fungal PRR that can couple to the Syk–CARD9 innate signaling pathway to activate DCs and regulate adaptive immune responses to fungal infection. |
format | Text |
id | pubmed-2737172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27371722010-02-28 Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection Robinson, Matthew J. Osorio, Fabiola Rosas, Marcela Freitas, Rui P. Schweighoffer, Edina Groß, Olaf Verbeek, J. Sjef Ruland, Jürgen Tybulewicz, Victor Brown, Gordon D. Moita, Luis Ferreira Taylor, Philip R. Reis e Sousa, Caetano J Exp Med Article Innate immune cells detect pathogens via pattern recognition receptors (PRRs), which signal for initiation of immune responses to infection. Studies with Dectin-1, a PRR for fungi, have defined a novel innate signaling pathway involving Syk kinase and the adaptor CARD9, which is critical for inducing Th17 responses to fungal infection. We show that another C-type lectin, Dectin-2, also signals via Syk and CARD9, and contributes to dendritic cell (DC) activation by fungal particles. Unlike Dectin-1, Dectin-2 couples to Syk indirectly, through association with the FcRγ chain. In a model of Candida albicans infection, blockade of Dectin-2 did not affect innate immune resistance but abrogated Candida-specific T cell production of IL-17 and, in combination with the absence of Dectin-1, decreased Th1 responses to the organism. Thus, Dectin-2 constitutes a major fungal PRR that can couple to the Syk–CARD9 innate signaling pathway to activate DCs and regulate adaptive immune responses to fungal infection. The Rockefeller University Press 2009-08-31 /pmc/articles/PMC2737172/ /pubmed/19703985 http://dx.doi.org/10.1084/jem.20082818 Text en © 2009 Robinson et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article Robinson, Matthew J. Osorio, Fabiola Rosas, Marcela Freitas, Rui P. Schweighoffer, Edina Groß, Olaf Verbeek, J. Sjef Ruland, Jürgen Tybulewicz, Victor Brown, Gordon D. Moita, Luis Ferreira Taylor, Philip R. Reis e Sousa, Caetano Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection |
title | Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection |
title_full | Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection |
title_fullStr | Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection |
title_full_unstemmed | Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection |
title_short | Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection |
title_sort | dectin-2 is a syk-coupled pattern recognition receptor crucial for th17 responses to fungal infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737172/ https://www.ncbi.nlm.nih.gov/pubmed/19703985 http://dx.doi.org/10.1084/jem.20082818 |
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