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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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The Rockefeller University Press
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584166/ https://www.ncbi.nlm.nih.gov/pubmed/28724527 http://dx.doi.org/10.1083/jcb.201701047 |