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Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells
The intestinal tract contains over half of all immune cells and peripheral nerves and manages the beneficial interactions between food compounds and the host. Paramylon is a β-1,3-glucan storage polysaccharide from Euglena gracilis (Euglena) that exerts immunostimulatory activities by affecting cyto...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468862/ https://www.ncbi.nlm.nih.gov/pubmed/32751743 http://dx.doi.org/10.3390/nu12082293 |
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author | Yasuda, Kosuke Nakashima, Ayaka Murata, Ako Suzuki, Kengo Adachi, Takahiro |
author_facet | Yasuda, Kosuke Nakashima, Ayaka Murata, Ako Suzuki, Kengo Adachi, Takahiro |
author_sort | Yasuda, Kosuke |
collection | PubMed |
description | The intestinal tract contains over half of all immune cells and peripheral nerves and manages the beneficial interactions between food compounds and the host. Paramylon is a β-1,3-glucan storage polysaccharide from Euglena gracilis (Euglena) that exerts immunostimulatory activities by affecting cytokine production. This study investigated the signaling mechanisms that regulate the beneficial interactions between food compounds and the intestinal tract using cell type-specific calcium (Ca(2+)) imaging in vivo and in vitro. We successfully visualized Euglena- and paramylon-mediated Ca(2+) signaling in vivo in intestinal epithelial cells from mice ubiquitously expressing the Yellow Cameleon 3.60 (YC3.60) Ca(2+) biosensor. Moreover, in vivo Ca(2+) imaging demonstrated that the intraperitoneal injection of both Euglena and paramylon stimulated dendritic cells (DCs) in Peyer’s patches, indicating that paramylon is an active component of Euglena that affects the immune system. In addition, in vitro Ca(2+) imaging in dorsal root ganglia indicated that Euglena, but not paramylon, triggers Ca(2+) signaling in the sensory nervous system innervating the intestine. Thus, this study is the first to successfully visualize the direct effect of β-1,3-glucan on DCs in vivo and will help elucidate the mechanisms via which Euglena and paramylon exert various effects in the intestinal tract. |
format | Online Article Text |
id | pubmed-7468862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74688622020-09-04 Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells Yasuda, Kosuke Nakashima, Ayaka Murata, Ako Suzuki, Kengo Adachi, Takahiro Nutrients Article The intestinal tract contains over half of all immune cells and peripheral nerves and manages the beneficial interactions between food compounds and the host. Paramylon is a β-1,3-glucan storage polysaccharide from Euglena gracilis (Euglena) that exerts immunostimulatory activities by affecting cytokine production. This study investigated the signaling mechanisms that regulate the beneficial interactions between food compounds and the intestinal tract using cell type-specific calcium (Ca(2+)) imaging in vivo and in vitro. We successfully visualized Euglena- and paramylon-mediated Ca(2+) signaling in vivo in intestinal epithelial cells from mice ubiquitously expressing the Yellow Cameleon 3.60 (YC3.60) Ca(2+) biosensor. Moreover, in vivo Ca(2+) imaging demonstrated that the intraperitoneal injection of both Euglena and paramylon stimulated dendritic cells (DCs) in Peyer’s patches, indicating that paramylon is an active component of Euglena that affects the immune system. In addition, in vitro Ca(2+) imaging in dorsal root ganglia indicated that Euglena, but not paramylon, triggers Ca(2+) signaling in the sensory nervous system innervating the intestine. Thus, this study is the first to successfully visualize the direct effect of β-1,3-glucan on DCs in vivo and will help elucidate the mechanisms via which Euglena and paramylon exert various effects in the intestinal tract. MDPI 2020-07-30 /pmc/articles/PMC7468862/ /pubmed/32751743 http://dx.doi.org/10.3390/nu12082293 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yasuda, Kosuke Nakashima, Ayaka Murata, Ako Suzuki, Kengo Adachi, Takahiro Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells |
title | Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells |
title_full | Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells |
title_fullStr | Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells |
title_full_unstemmed | Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells |
title_short | Euglena Gracilis and β-Glucan Paramylon Induce Ca(2+) Signaling in Intestinal Tract Epithelial, Immune, and Neural Cells |
title_sort | euglena gracilis and β-glucan paramylon induce ca(2+) signaling in intestinal tract epithelial, immune, and neural cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468862/ https://www.ncbi.nlm.nih.gov/pubmed/32751743 http://dx.doi.org/10.3390/nu12082293 |
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