Glial activation in prion diseases is selectively triggered by neuronal PrP <sup>Sc</sup>-Reference-Cited by-同舟云学术

Glial activation in prion diseases is selectively triggered by neuronal PrP ^Sc

Published:2022-02-17 Issue:5 Volume:32 Page:
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Lakkaraju Asvin K. K.¹^ORCID,Sorce Silvia¹^ORCID,Senatore Assunta¹^ORCID,Nuvolone Mario¹²³,Guo Jingjing¹^ORCID,Schwarz Petra¹,Moos Rita¹,Pelczar Pawel⁴^ORCID,Aguzzi Adriano¹^ORCID

Affiliation:

1. Institute of Neuropathology University Hospital of Zurich Zurich Switzerland

2. Amyloidosis Research and Treatment Center Foundation Scientific Institute Policlinico San Matteo Pavia Italy

3. Department of Molecular Medicine University of Pavia Pavia Italy

4. Center for Transgenic Models University of Basel Basel Switzerland

Funder

Stiftung Synapsis - Alzheimer Forschung Schweiz AFS

SystemsX.ch

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

H2020 European Research Council

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.13056

Reference36 articles.

1. Beyond the prion principle

2. Mice devoid of PrP are resistant to scrapie

3. Normal host prion protein necessary for scrapie-induced neurotoxicity

4. Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system

5. The immunobiology of prion diseases

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