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Prions amplify through degradation of the VPS10P sorting receptor sortilin

  • Published:2017-06-30 Issue:6 Volume:13 Page:e1006470
  • ISSN:1553-7374
  • Container-title:PLOS Pathogens
  • language:en
  • Short-container-title:PLoS Pathog

Author:

Uchiyama KeijiORCID,Tomita Mitsuru,Yano Masashi,Chida JunjiORCID,Hara Hideyuki,Das Nandita RaniORCID,Nykjaer Anders,Sakaguchi SuehiroORCID

Funder

Pilot Research Support Program in Tokushima University

Naito Foundation

JSPS KAKENHI grant

MEXT KAKENHI grant

the Practical Research Project for Rare/Intractable Diseases of the Japan Agency for Medical Research and Development (AMED)

Publisher

Public Library of Science (PLoS)

Subject

Virology,Genetics,Molecular Biology,Immunology,Microbiology,Parasitology

Reference37 articles.

1. Prions;SB Prusiner;Proc Natl Acad Sci U S A,1998

2. Mice devoid of PrP are resistant to scrapie;H Bueler;Cell,1993

3. Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies;SB Prusiner;Proc Natl Acad Sci U S A,1993

4. PrP gene dosage determines the timing but not the final intensity or distribution of lesions in scrapie pathology;JC Manson;Neurodegeneration,1994

5. Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent;S Sakaguchi;J Virol,1995

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