Cellular Prion Protein Mediates α-Synuclein Uptake, Localization, and Toxicity In Vitro and In Vivo.
Tobias ThomMatthias SchmitzAnna-Lisa FischerAngela CorreiaSusana CorreiaFranc LlorensAnna-Villar PiqueWiebke MöbiusRenato DominguesSaima ZafarErik StoopsChristopher J SilvaAndre FischerTiago F OuteiroInga ZerrPublished in: Movement disorders : official journal of the Movement Disorder Society (2021)
PrPC 's native trafficking can be misused to internalize misfolded aSyn through a clathrin-based mechanism, which may facilitate the spreading of pathological aSyn. Disruption of aSyn-PrPC binding is, therefore, an appealing therapeutic target in α-synucleinopathies. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.