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IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans

IL-33 is a member of the IL-1 cytokine family and plays a role in the host defense against bacteria, viruses, and fungi. In this study, we investigated the function of IL-33 and its receptor in in vitro macrophage responses to Candida albicans. Our results demonstrate that pre-sensitization of isola...

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Detalles Bibliográficos
Autores principales: Tran, Vuvi G., Cho, Hong R., Kwon, Byungsuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148490/
https://www.ncbi.nlm.nih.gov/pubmed/25177252
http://dx.doi.org/10.4110/in.2014.14.4.201
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author Tran, Vuvi G.
Cho, Hong R.
Kwon, Byungsuk
author_facet Tran, Vuvi G.
Cho, Hong R.
Kwon, Byungsuk
author_sort Tran, Vuvi G.
collection PubMed
description IL-33 is a member of the IL-1 cytokine family and plays a role in the host defense against bacteria, viruses, and fungi. In this study, we investigated the function of IL-33 and its receptor in in vitro macrophage responses to Candida albicans. Our results demonstrate that pre-sensitization of isolated peritoneal macrophages with IL-33 enhanced their pro-inflammatory cytokine production and phagocytic activity in response to C. albicans. These macrophage activities were entirely dependent on the ST2-MyD88 signaling pathway. In addition, pre-sensitization with IL-33 also increased ROS production and the subsequent killing ability of macrophages following C. albicans challenge. These results indicate that IL-33 may increase anti-fungal activity against Candida through macrophage-mediated resistance mechanisms.
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spelling pubmed-41484902014-08-29 IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans Tran, Vuvi G. Cho, Hong R. Kwon, Byungsuk Immune Netw Original Article IL-33 is a member of the IL-1 cytokine family and plays a role in the host defense against bacteria, viruses, and fungi. In this study, we investigated the function of IL-33 and its receptor in in vitro macrophage responses to Candida albicans. Our results demonstrate that pre-sensitization of isolated peritoneal macrophages with IL-33 enhanced their pro-inflammatory cytokine production and phagocytic activity in response to C. albicans. These macrophage activities were entirely dependent on the ST2-MyD88 signaling pathway. In addition, pre-sensitization with IL-33 also increased ROS production and the subsequent killing ability of macrophages following C. albicans challenge. These results indicate that IL-33 may increase anti-fungal activity against Candida through macrophage-mediated resistance mechanisms. The Korean Association of Immunologists 2014-08 2014-08-22 /pmc/articles/PMC4148490/ /pubmed/25177252 http://dx.doi.org/10.4110/in.2014.14.4.201 Text en Copyright © 2014 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tran, Vuvi G.
Cho, Hong R.
Kwon, Byungsuk
IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans
title IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans
title_full IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans
title_fullStr IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans
title_full_unstemmed IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans
title_short IL-33 Priming Enhances Peritoneal Macrophage Activity in Response to Candida albicans
title_sort il-33 priming enhances peritoneal macrophage activity in response to candida albicans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148490/
https://www.ncbi.nlm.nih.gov/pubmed/25177252
http://dx.doi.org/10.4110/in.2014.14.4.201
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