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Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cells
Prions are proteinaceous infectious particles which cause fatal neurodegenerative disorders in humans and animals. They consist of a mostly β-sheeted aggregated isoform (PrP(Sc)) of the cellular prion protein (PrP(c)). Prions replicate autocatalytically in neurons and other cell types by inducing co...
Autores principales: | Shim, Su Yeon, Karri, Srinivasarao, Law, Sampson, Schatzl, Hermann M., Gilch, Sabine |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749993/ https://www.ncbi.nlm.nih.gov/pubmed/26865414 http://dx.doi.org/10.1038/srep21658 |
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