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The spread of prion-like proteins by lysosomes and tunneling nanotubes: Implications for neurodegenerative diseases

Progression of pathology in neurodegenerative diseases is hypothesized to be a non–cell-autonomous process that may be mediated by the productive spreading of prion-like protein aggregates from a “donor cell” that is the source of misfolded aggregates to an “acceptor cell” in which misfolding is pro...

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Bibliographic Details
Published in:J Cell Biol
Main Authors: Victoria, Guiliana Soraya, Zurzolo, Chiara
Format: Artigo
Language:Inglês
Published: The Rockefeller University Press 2017
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5584166/
https://ncbi.nlm.nih.gov/pubmed/28724527
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201701047
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