Abstract
Tau aggregation is a pathological hallmark of Alzheimer's disease, Parkinson's disease, and many other neurodegenerative disorders known as tauopathies. Tau aggregates take on many forms, and their formation is a multistage process with intermediate stages. Recently, tau oligomers have emerged as the pathogenic species in tauopathies and a possible mediator of amyloid-β toxicity in Alzheimer's disease. Here, we use a novel, physiologically relevant method (oligomer cross-seeding) to prepare homogeneous populations of tau oligomers and characterize these oligomers in vitro. We show that both Aβ and α-synuclein oligomers induce tau aggregation and the formation of β-sheet-rich neurotoxic tau oligomers.
Original language | English (US) |
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Pages (from-to) | 10039-10041 |
Number of pages | 3 |
Journal | Biochemistry |
Volume | 49 |
Issue number | 47 |
DOIs | |
State | Published - Nov 30 2010 |
ASJC Scopus subject areas
- Biochemistry