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Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells

Tolerogenic dendritic cells (DCs) have the ability to induce regulatory T cells and play an important role in preventing chronic inflammatory and autoimmune diseases. We have identified a novel compound, 14-dehydroergosterol, from Koji, a Japanese traditional food material fermented with fungi. 14-d...

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Autores principales: Ano, Yasuhisa, Ikado, Kumiko, Shindo, Kazutoshi, Koizumi, Hideki, Fujiwara, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654777/
https://www.ncbi.nlm.nih.gov/pubmed/29066789
http://dx.doi.org/10.1038/s41598-017-14446-1
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author Ano, Yasuhisa
Ikado, Kumiko
Shindo, Kazutoshi
Koizumi, Hideki
Fujiwara, Daisuke
author_facet Ano, Yasuhisa
Ikado, Kumiko
Shindo, Kazutoshi
Koizumi, Hideki
Fujiwara, Daisuke
author_sort Ano, Yasuhisa
collection PubMed
description Tolerogenic dendritic cells (DCs) have the ability to induce regulatory T cells and play an important role in preventing chronic inflammatory and autoimmune diseases. We have identified a novel compound, 14-dehydroergosterol, from Koji, a Japanese traditional food material fermented with fungi. 14-dehydroergosterol is an ergosterol analogue with a conjugated double bond, but the activity of 14-dehydroergosterol is much higher than that of ergosterol. 14-dehydroergosterol induces the conversion of murine bone marrow (BM)-derived DCs and differentiated DCs into tolerogenic DCs, in which the production of IL-12 is suppressed and that of IL-10 is increased. In a co-culture experiment, DCs treated with 14-dehydroergosterol induced the conversion of naïve CD4-positive T cells into regulatory T cells. In a murine model of multiple sclerosis, experimental autoimmune encephalopathy, 14-dehydroergosterol suppressed the clinical score and inflammatory responses of myeloid DCs and T cells to myelin oligodendrocyte glycoprotein. 14-dehydroergosterol-treated human DCs induced from PBMCs also showed a tolerogenic phenotype. This is the first report to identify a novel compound, 14-dehydroergosterol, that induces DCs to convert to a tolerogenic type. 14-dehydroergosterol is contained in various fermented foods based on Koji, so 14-dehydroergosterol might be a helpful aid to prevent chronic inflammatory and autoimmune diseases.
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spelling pubmed-56547772017-10-31 Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells Ano, Yasuhisa Ikado, Kumiko Shindo, Kazutoshi Koizumi, Hideki Fujiwara, Daisuke Sci Rep Article Tolerogenic dendritic cells (DCs) have the ability to induce regulatory T cells and play an important role in preventing chronic inflammatory and autoimmune diseases. We have identified a novel compound, 14-dehydroergosterol, from Koji, a Japanese traditional food material fermented with fungi. 14-dehydroergosterol is an ergosterol analogue with a conjugated double bond, but the activity of 14-dehydroergosterol is much higher than that of ergosterol. 14-dehydroergosterol induces the conversion of murine bone marrow (BM)-derived DCs and differentiated DCs into tolerogenic DCs, in which the production of IL-12 is suppressed and that of IL-10 is increased. In a co-culture experiment, DCs treated with 14-dehydroergosterol induced the conversion of naïve CD4-positive T cells into regulatory T cells. In a murine model of multiple sclerosis, experimental autoimmune encephalopathy, 14-dehydroergosterol suppressed the clinical score and inflammatory responses of myeloid DCs and T cells to myelin oligodendrocyte glycoprotein. 14-dehydroergosterol-treated human DCs induced from PBMCs also showed a tolerogenic phenotype. This is the first report to identify a novel compound, 14-dehydroergosterol, that induces DCs to convert to a tolerogenic type. 14-dehydroergosterol is contained in various fermented foods based on Koji, so 14-dehydroergosterol might be a helpful aid to prevent chronic inflammatory and autoimmune diseases. Nature Publishing Group UK 2017-10-24 /pmc/articles/PMC5654777/ /pubmed/29066789 http://dx.doi.org/10.1038/s41598-017-14446-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ano, Yasuhisa
Ikado, Kumiko
Shindo, Kazutoshi
Koizumi, Hideki
Fujiwara, Daisuke
Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
title Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
title_full Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
title_fullStr Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
title_full_unstemmed Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
title_short Identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
title_sort identification of 14-dehydroergosterol as a novel anti-inflammatory compound inducing tolerogenic dendritic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654777/
https://www.ncbi.nlm.nih.gov/pubmed/29066789
http://dx.doi.org/10.1038/s41598-017-14446-1
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