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Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease

The accumulation of amyloid-β protein (Aβ) in brain is linked to the early pathogenesis of Alzheimer’s disease (AD). We previously reported that neuron-derived exosomes promote Aβ clearance in the brains of amyloid precursor protein transgenic mice and that exosome production is modulated by ceramid...

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Autores principales: Yuyama, Kohei, Takahashi, Kaori, Usuki, Seigo, Mikami, Daisuke, Sun, Hui, Hanamatsu, Hisatoshi, Furukawa, Junichi, Mukai, Katsuyuki, Igarashi, Yasuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856149/
https://www.ncbi.nlm.nih.gov/pubmed/31727994
http://dx.doi.org/10.1038/s41598-019-53394-w
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author Yuyama, Kohei
Takahashi, Kaori
Usuki, Seigo
Mikami, Daisuke
Sun, Hui
Hanamatsu, Hisatoshi
Furukawa, Junichi
Mukai, Katsuyuki
Igarashi, Yasuyuki
author_facet Yuyama, Kohei
Takahashi, Kaori
Usuki, Seigo
Mikami, Daisuke
Sun, Hui
Hanamatsu, Hisatoshi
Furukawa, Junichi
Mukai, Katsuyuki
Igarashi, Yasuyuki
author_sort Yuyama, Kohei
collection PubMed
description The accumulation of amyloid-β protein (Aβ) in brain is linked to the early pathogenesis of Alzheimer’s disease (AD). We previously reported that neuron-derived exosomes promote Aβ clearance in the brains of amyloid precursor protein transgenic mice and that exosome production is modulated by ceramide metabolism. Here, we demonstrate that plant ceramides derived from Amorphophallus konjac, as well as animal-derived ceramides, enhanced production of extracellular vesicles (EVs) in neuronal cultures. Oral administration of plant glucosylceramide (GlcCer) to APP overexpressing mice markedly reduced Aβ levels and plaque burdens and improved cognition in a Y-maze learning task. Moreover, there were substantial increases in the neuronal marker NCAM-1, L1CAM, and Aβ in EVs isolated from serum and brain tissues of the GlcCer-treated AD model mice. Our data showing that plant ceramides prevent Aβ accumulation by promoting EVs-dependent Aβ clearance in vitro and in vivo provide evidence for a protective role of plant ceramides in AD. Plant ceramides might thus be used as functional food materials to ameliorate AD pathology.
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spelling pubmed-68561492019-11-19 Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease Yuyama, Kohei Takahashi, Kaori Usuki, Seigo Mikami, Daisuke Sun, Hui Hanamatsu, Hisatoshi Furukawa, Junichi Mukai, Katsuyuki Igarashi, Yasuyuki Sci Rep Article The accumulation of amyloid-β protein (Aβ) in brain is linked to the early pathogenesis of Alzheimer’s disease (AD). We previously reported that neuron-derived exosomes promote Aβ clearance in the brains of amyloid precursor protein transgenic mice and that exosome production is modulated by ceramide metabolism. Here, we demonstrate that plant ceramides derived from Amorphophallus konjac, as well as animal-derived ceramides, enhanced production of extracellular vesicles (EVs) in neuronal cultures. Oral administration of plant glucosylceramide (GlcCer) to APP overexpressing mice markedly reduced Aβ levels and plaque burdens and improved cognition in a Y-maze learning task. Moreover, there were substantial increases in the neuronal marker NCAM-1, L1CAM, and Aβ in EVs isolated from serum and brain tissues of the GlcCer-treated AD model mice. Our data showing that plant ceramides prevent Aβ accumulation by promoting EVs-dependent Aβ clearance in vitro and in vivo provide evidence for a protective role of plant ceramides in AD. Plant ceramides might thus be used as functional food materials to ameliorate AD pathology. Nature Publishing Group UK 2019-11-14 /pmc/articles/PMC6856149/ /pubmed/31727994 http://dx.doi.org/10.1038/s41598-019-53394-w Text en © The Author(s) 2019 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
Yuyama, Kohei
Takahashi, Kaori
Usuki, Seigo
Mikami, Daisuke
Sun, Hui
Hanamatsu, Hisatoshi
Furukawa, Junichi
Mukai, Katsuyuki
Igarashi, Yasuyuki
Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease
title Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease
title_full Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease
title_fullStr Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease
title_full_unstemmed Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease
title_short Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer’s disease
title_sort plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856149/
https://www.ncbi.nlm.nih.gov/pubmed/31727994
http://dx.doi.org/10.1038/s41598-019-53394-w
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