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Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells
In our previous study, we demonstrated the propagation of mouse-passaged scrapie isolates with long incubation periods (L-type) derived from natural Japanese sheep scrapie cases in murine hypothalamic GT1-7 cells, along with disease-associated prion protein (PrP(Sc)) accumulation. We here analyzed t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479544/ https://www.ncbi.nlm.nih.gov/pubmed/28636656 http://dx.doi.org/10.1371/journal.pone.0179317 |
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author | Miyazawa, Kohtaro Masujin, Kentaro Okada, Hiroyuki Ushiki-Kaku, Yuko Matsuura, Yuichi Yokoyama, Takashi |
author_facet | Miyazawa, Kohtaro Masujin, Kentaro Okada, Hiroyuki Ushiki-Kaku, Yuko Matsuura, Yuichi Yokoyama, Takashi |
author_sort | Miyazawa, Kohtaro |
collection | PubMed |
description | In our previous study, we demonstrated the propagation of mouse-passaged scrapie isolates with long incubation periods (L-type) derived from natural Japanese sheep scrapie cases in murine hypothalamic GT1-7 cells, along with disease-associated prion protein (PrP(Sc)) accumulation. We here analyzed the susceptibility of GT1-7 cells to scrapie prions by exposure to infected mouse brains at different passages, following interspecies transmission. Wild-type mice challenged with a natural sheep scrapie case (Kanagawa) exhibited heterogeneity of transmitted scrapie prions in early passages, and this mixed population converged upon one with a short incubation period (S-type) following subsequent passages. However, when GT1-7 cells were challenged with these heterologous samples, L-type prions became dominant. This study demonstrated that the susceptibility of GT1-7 cells to L-type prions was at least 10(5) times higher than that to S-type prions and that L-type prion-specific biological characteristics remained unchanged after serial passages in GT1-7 cells. This suggests that a GT1-7 cell culture model would be more useful for the economical and stable amplification of L-type prions at the laboratory level. Furthermore, this cell culture model might be used to selectively propagate L-type scrapie prions from a mixed prion population. |
format | Online Article Text |
id | pubmed-5479544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54795442017-07-05 Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells Miyazawa, Kohtaro Masujin, Kentaro Okada, Hiroyuki Ushiki-Kaku, Yuko Matsuura, Yuichi Yokoyama, Takashi PLoS One Research Article In our previous study, we demonstrated the propagation of mouse-passaged scrapie isolates with long incubation periods (L-type) derived from natural Japanese sheep scrapie cases in murine hypothalamic GT1-7 cells, along with disease-associated prion protein (PrP(Sc)) accumulation. We here analyzed the susceptibility of GT1-7 cells to scrapie prions by exposure to infected mouse brains at different passages, following interspecies transmission. Wild-type mice challenged with a natural sheep scrapie case (Kanagawa) exhibited heterogeneity of transmitted scrapie prions in early passages, and this mixed population converged upon one with a short incubation period (S-type) following subsequent passages. However, when GT1-7 cells were challenged with these heterologous samples, L-type prions became dominant. This study demonstrated that the susceptibility of GT1-7 cells to L-type prions was at least 10(5) times higher than that to S-type prions and that L-type prion-specific biological characteristics remained unchanged after serial passages in GT1-7 cells. This suggests that a GT1-7 cell culture model would be more useful for the economical and stable amplification of L-type prions at the laboratory level. Furthermore, this cell culture model might be used to selectively propagate L-type scrapie prions from a mixed prion population. Public Library of Science 2017-06-21 /pmc/articles/PMC5479544/ /pubmed/28636656 http://dx.doi.org/10.1371/journal.pone.0179317 Text en © 2017 Miyazawa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Miyazawa, Kohtaro Masujin, Kentaro Okada, Hiroyuki Ushiki-Kaku, Yuko Matsuura, Yuichi Yokoyama, Takashi Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
title | Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
title_full | Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
title_fullStr | Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
title_full_unstemmed | Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
title_short | Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
title_sort | selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using gt1-7 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479544/ https://www.ncbi.nlm.nih.gov/pubmed/28636656 http://dx.doi.org/10.1371/journal.pone.0179317 |
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