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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of Neuroscie...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of Neuroscience Research
Article . 2010 . Peer-reviewed
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Amyloid β accelerates phosphorylation of tau and neurofibrillary tangle formation in an amyloid precursor protein and tau double‐transgenic mouse model

Authors: Tetsuro Murakami; Masaki Ikeda; Etsuro Matsubara; Yukiko Yamamoto-Watanabe; Yasuhito Wakasaya; Takeshi Kawarabayashi; Mitsunori Watanabe; +7 Authors

Amyloid β accelerates phosphorylation of tau and neurofibrillary tangle formation in an amyloid precursor protein and tau double‐transgenic mouse model

Abstract

AbstractIn Alzheimer's disease, Aβ deposits are considered the initial cardinal events that induce tauopathy secondarily. However, the relationship between Aβ amyloidosis and tauopathy has not been determined in detail. We produced double transgenic mice, 2×TgTau+/–APP+/–, by mating Tg2576 mice that exhibit Aβ amyloidosis and TgTauP301L mice that show tauopathy, and statistically analyzed the effect of Aβ accumulation on tauopathy. There was no significant difference in theprogression of Aβ accumulation among 2×TgTau+/–APP+/– and 1×TgTau−/–APP+/–, and tau accumulation among 2×TgTau+/−APP+/− and 1×Tg Tau+/–APP−/–. The appearance rates of phosphorylated tau developing in neurons and processes were significantly accelerated in 2×TgTau+/–APP+/– mice compared with those in 1×TgTau+/–APP−/– mice at 23 months of age. Accumulation of phosphorylated and confomationally altered tau and GSK3β in neuronal processes was accelerated in the white matter in 2×TgTau+/–APP+/–. The level of phosphorylated tau in the sarkosyl‐insoluble fraction was increased in 2×TgTau+/–APP+/– brains compared with that in 1×TgTau+/–APP−/– brains. Thus, Aβ amyloid partially enhances tauopathy through accumulation of insoluble, phosphorylated, and conformationally changed tau in neuronal cytoplasm and processes in the late stage. © 2010 Wiley‐Liss, Inc.

Keywords

Neurons, Brain Diseases, Amyloid beta-Peptides, Age Factors, Mice, Transgenic, Neurofibrillary Tangles, tau Proteins, Amyloid Neuropathies, Amyloid beta-Protein Precursor, Disease Models, Animal, Mice, Tauopathies, Animals, Longitudinal Studies

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
27
Top 10%
Top 10%
Average
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