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M cell-depletion blocks oral prion disease pathogenesis

Many prion diseases are orally acquired. Our data show that after oral exposure, early prion replication upon follicular dendritic cells (FDC) in Peyer's patches is obligatory for the efficient spread of disease to the brain (termed neuroinvasion). For prions to replicate on FDC within Peyer�...

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Autores principales: Donaldson, D S, Kobayashi, A, Ohno, H, Yagita, H, Williams, I R, Mabbott, N A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282432/
https://www.ncbi.nlm.nih.gov/pubmed/22294048
http://dx.doi.org/10.1038/mi.2011.68
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author Donaldson, D S
Kobayashi, A
Ohno, H
Yagita, H
Williams, I R
Mabbott, N A
author_facet Donaldson, D S
Kobayashi, A
Ohno, H
Yagita, H
Williams, I R
Mabbott, N A
author_sort Donaldson, D S
collection PubMed
description Many prion diseases are orally acquired. Our data show that after oral exposure, early prion replication upon follicular dendritic cells (FDC) in Peyer's patches is obligatory for the efficient spread of disease to the brain (termed neuroinvasion). For prions to replicate on FDC within Peyer's patches after ingestion of a contaminated meal, they must first cross the gut epithelium. However, the mechanism through which prions are conveyed into Peyer's patches is uncertain. Within the follicle-associated epithelium overlying Peyer's patches are microfold cells (M cells), unique epithelial cells specialized for the transcytosis of particles. We show that following M cell-depletion, early prion accumulation upon FDC in Peyer's patches is blocked. Furthermore, in the absence of M cells at the time of oral exposure, neuroinvasion and disease development are likewise blocked. These data suggest M cells are important sites of prion uptake from the gut lumen into Peyer's patches.
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spelling pubmed-32824322012-02-21 M cell-depletion blocks oral prion disease pathogenesis Donaldson, D S Kobayashi, A Ohno, H Yagita, H Williams, I R Mabbott, N A Mucosal Immunol Article Many prion diseases are orally acquired. Our data show that after oral exposure, early prion replication upon follicular dendritic cells (FDC) in Peyer's patches is obligatory for the efficient spread of disease to the brain (termed neuroinvasion). For prions to replicate on FDC within Peyer's patches after ingestion of a contaminated meal, they must first cross the gut epithelium. However, the mechanism through which prions are conveyed into Peyer's patches is uncertain. Within the follicle-associated epithelium overlying Peyer's patches are microfold cells (M cells), unique epithelial cells specialized for the transcytosis of particles. We show that following M cell-depletion, early prion accumulation upon FDC in Peyer's patches is blocked. Furthermore, in the absence of M cells at the time of oral exposure, neuroinvasion and disease development are likewise blocked. These data suggest M cells are important sites of prion uptake from the gut lumen into Peyer's patches. Nature Publishing Group 2012-03 2012-02-01 /pmc/articles/PMC3282432/ /pubmed/22294048 http://dx.doi.org/10.1038/mi.2011.68 Text en Copyright © 2012 Society for Mucosal Immunology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Donaldson, D S
Kobayashi, A
Ohno, H
Yagita, H
Williams, I R
Mabbott, N A
M cell-depletion blocks oral prion disease pathogenesis
title M cell-depletion blocks oral prion disease pathogenesis
title_full M cell-depletion blocks oral prion disease pathogenesis
title_fullStr M cell-depletion blocks oral prion disease pathogenesis
title_full_unstemmed M cell-depletion blocks oral prion disease pathogenesis
title_short M cell-depletion blocks oral prion disease pathogenesis
title_sort m cell-depletion blocks oral prion disease pathogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282432/
https://www.ncbi.nlm.nih.gov/pubmed/22294048
http://dx.doi.org/10.1038/mi.2011.68
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