Cargando…
Secretory pathway retention of mutant prion protein induces p38-MAPK activation and lethal disease in mice
Misfolding of proteins in the biosynthetic pathway in neurons may cause disturbed protein homeostasis and neurodegeneration. The prion protein (PrP(C)) is a GPI-anchored protein that resides at the plasma membrane and may be misfolded to PrP(Sc) leading to prion diseases. We show that a deletion in...
Autores principales: | Puig, Berta, Altmeppen, Hermann C., Ulbrich, Sarah, Linsenmeier, Luise, Krasemann, Susanne, Chakroun, Karima, Acevedo-Morantes, Claudia Y., Wille, Holger, Tatzelt, Jörg, Glatzel, Markus |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847012/ https://www.ncbi.nlm.nih.gov/pubmed/27117504 http://dx.doi.org/10.1038/srep24970 |
Ejemplares similares
-
GPI-anchor signal sequence influences PrP(C) sorting, shedding and signalling, and impacts on different pathomechanistic aspects of prion disease in mice
por: Puig, Berta, et al.
Publicado: (2019) -
Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein
por: Linsenmeier, Luise, et al.
Publicado: (2018) -
The sheddase ADAM10 is a potent modulator of prion disease
por: Altmeppen, Hermann C, et al.
Publicado: (2015) -
Transgenic Overexpression of the Disordered Prion Protein N1 Fragment in Mice Does Not Protect Against Neurodegenerative Diseases Due to Impaired ER Translocation
por: Mohammadi, Behnam, et al.
Publicado: (2020) -
The Structure of Human Prions: From Biology to Structural Models — Considerations and Pitfalls
por: Acevedo-Morantes, Claudia Y., et al.
Publicado: (2014)