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The multivesicular body is the major internal site of prion conversion

The conversion of the properly folded prion protein, PrPc, to its misfolded amyloid form, PrPsc, occurs as the two proteins traffic along the endocytic pathway and PrPc is exposed to PrPsc. To determine the specific site of prion conversion, we knocked down various proteins in the endocytic pathway...

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Autores principales: Yim, Yang-In, Park, Bum-Chan, Yadavalli, Rajgopal, Zhao, Xiaohong, Eisenberg, Evan, Greene, Lois E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379730/
https://www.ncbi.nlm.nih.gov/pubmed/25663703
http://dx.doi.org/10.1242/jcs.165472
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author Yim, Yang-In
Park, Bum-Chan
Yadavalli, Rajgopal
Zhao, Xiaohong
Eisenberg, Evan
Greene, Lois E.
author_facet Yim, Yang-In
Park, Bum-Chan
Yadavalli, Rajgopal
Zhao, Xiaohong
Eisenberg, Evan
Greene, Lois E.
author_sort Yim, Yang-In
collection PubMed
description The conversion of the properly folded prion protein, PrPc, to its misfolded amyloid form, PrPsc, occurs as the two proteins traffic along the endocytic pathway and PrPc is exposed to PrPsc. To determine the specific site of prion conversion, we knocked down various proteins in the endocytic pathway including Rab7a, Tsg101 and Hrs (also known as HGS). PrPsc was markedly reduced in two chronically infected cell lines by preventing the maturation of the multivesicular body, a process that begins in the early endosome and ends with the sorting of cargo to the lysosome. By contrast, knocking down proteins in the retromer complex, which diverts cargo away from the multivesicular body caused an increase in PrPsc levels. These results suggest that the multivesicular body is the major site for intracellular conversion of PrPc to PrPsc.
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spelling pubmed-43797302015-04-13 The multivesicular body is the major internal site of prion conversion Yim, Yang-In Park, Bum-Chan Yadavalli, Rajgopal Zhao, Xiaohong Eisenberg, Evan Greene, Lois E. J Cell Sci Research Article The conversion of the properly folded prion protein, PrPc, to its misfolded amyloid form, PrPsc, occurs as the two proteins traffic along the endocytic pathway and PrPc is exposed to PrPsc. To determine the specific site of prion conversion, we knocked down various proteins in the endocytic pathway including Rab7a, Tsg101 and Hrs (also known as HGS). PrPsc was markedly reduced in two chronically infected cell lines by preventing the maturation of the multivesicular body, a process that begins in the early endosome and ends with the sorting of cargo to the lysosome. By contrast, knocking down proteins in the retromer complex, which diverts cargo away from the multivesicular body caused an increase in PrPsc levels. These results suggest that the multivesicular body is the major site for intracellular conversion of PrPc to PrPsc. The Company of Biologists 2015-04-01 /pmc/articles/PMC4379730/ /pubmed/25663703 http://dx.doi.org/10.1242/jcs.165472 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Yim, Yang-In
Park, Bum-Chan
Yadavalli, Rajgopal
Zhao, Xiaohong
Eisenberg, Evan
Greene, Lois E.
The multivesicular body is the major internal site of prion conversion
title The multivesicular body is the major internal site of prion conversion
title_full The multivesicular body is the major internal site of prion conversion
title_fullStr The multivesicular body is the major internal site of prion conversion
title_full_unstemmed The multivesicular body is the major internal site of prion conversion
title_short The multivesicular body is the major internal site of prion conversion
title_sort multivesicular body is the major internal site of prion conversion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379730/
https://www.ncbi.nlm.nih.gov/pubmed/25663703
http://dx.doi.org/10.1242/jcs.165472
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