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Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo

β-Glucans are known for their ability to trigger both protective and damaging immune responses. Here we have explored the role of the beta-glucan receptor Dectin-1 in archetypical models of protective and non-protective immunomodulation induced by beta-glucan rich ligands. In the first model, we exp...

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Detalles Bibliográficos
Autores principales: Marakalala, Mohlopheni J., Williams, David L., Hoving, Jennifer C., Engstad, Rolf, Netea, Mihai G., Brown, Gordon D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839404/
https://www.ncbi.nlm.nih.gov/pubmed/23518266
http://dx.doi.org/10.1016/j.micinf.2013.03.002
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author Marakalala, Mohlopheni J.
Williams, David L.
Hoving, Jennifer C.
Engstad, Rolf
Netea, Mihai G.
Brown, Gordon D.
author_facet Marakalala, Mohlopheni J.
Williams, David L.
Hoving, Jennifer C.
Engstad, Rolf
Netea, Mihai G.
Brown, Gordon D.
author_sort Marakalala, Mohlopheni J.
collection PubMed
description β-Glucans are known for their ability to trigger both protective and damaging immune responses. Here we have explored the role of the beta-glucan receptor Dectin-1 in archetypical models of protective and non-protective immunomodulation induced by beta-glucan rich ligands. In the first model, we explored the role of Dectin-1 in the ability of soluble purified β-glucans to mediate protection against systemic Staphylococcus aureus infection in mice. In the second model, we explored the role of Dectin-1 in zymosan induced multiple organ dysfunction syndrome. In both cases, these β-glucan rich compounds had marked effects in vivo which were unaltered by Dectin-1 deficiency, suggesting that this receptor has a redundant role in these murine models.
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spelling pubmed-38394042013-11-26 Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo Marakalala, Mohlopheni J. Williams, David L. Hoving, Jennifer C. Engstad, Rolf Netea, Mihai G. Brown, Gordon D. Microbes Infect Short Communication β-Glucans are known for their ability to trigger both protective and damaging immune responses. Here we have explored the role of the beta-glucan receptor Dectin-1 in archetypical models of protective and non-protective immunomodulation induced by beta-glucan rich ligands. In the first model, we explored the role of Dectin-1 in the ability of soluble purified β-glucans to mediate protection against systemic Staphylococcus aureus infection in mice. In the second model, we explored the role of Dectin-1 in zymosan induced multiple organ dysfunction syndrome. In both cases, these β-glucan rich compounds had marked effects in vivo which were unaltered by Dectin-1 deficiency, suggesting that this receptor has a redundant role in these murine models. Elsevier 2013-06 /pmc/articles/PMC3839404/ /pubmed/23518266 http://dx.doi.org/10.1016/j.micinf.2013.03.002 Text en © 2013 Elsevier Masson SAS. https://creativecommons.org/licenses/by/4.0/ Open Access under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) license
spellingShingle Short Communication
Marakalala, Mohlopheni J.
Williams, David L.
Hoving, Jennifer C.
Engstad, Rolf
Netea, Mihai G.
Brown, Gordon D.
Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
title Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
title_full Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
title_fullStr Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
title_full_unstemmed Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
title_short Dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
title_sort dectin-1 plays a redundant role in the immunomodulatory activities of β-glucan-rich ligands in vivo
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839404/
https://www.ncbi.nlm.nih.gov/pubmed/23518266
http://dx.doi.org/10.1016/j.micinf.2013.03.002
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