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- W2399567181 abstract "Abstract 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 conformational conversion of PrP c into PrP Sc . Within neurons, PrP Sc accumulates at the plasma membrane and in vesicles of the endocytic pathway. To better understand the mechanisms underlying neuronal dysfunction and death it is critical to know the impact of PrP Sc accumulation on cellular pathways. We have investigated the effects of prion infection on endo-lysosomal transport. Our study demonstrates that prion infection interferes with rab7 membrane association. Consequently, lysosomal maturation and degradation are impaired. Our findings indicate a mechanism induced by prion infection that supports stable prion replication. We suggest modulation of endo-lysosomal vesicle trafficking and enhancement of lysosomal maturation as novel targets for the treatment of prion diseases." @default.
- W2399567181 created "2016-06-24" @default.
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- W2399567181 date "2016-02-11" @default.
- W2399567181 modified "2023-09-24" @default.
- W2399567181 title "Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cells" @default.
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- W2399567181 doi "https://doi.org/10.1038/srep21658" @default.
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