TY - JOUR
T1 - Preparation and characterization of neurotoxic tau oligomers
AU - Lasagna-Reeves, C.A.
AU - Castillo-Carranza, D.L.
AU - Guerrero-Muñoz, M.J.
AU - Jackson, G.R.
AU - Kayed, R.
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2010/11/30
Y1 - 2010/11/30
N2 - 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.
AB - 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.
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UR - https://www.mendeley.com/catalogue/e6946506-47ea-36b3-b024-a8d0f0ca330c/
U2 - 10.1021/bi1016233
DO - 10.1021/bi1016233
M3 - Article
SN - 0006-2960
VL - 49
SP - 10039
EP - 10041
JO - Biochemistry
JF - Biochemistry
IS - 47
ER -