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Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain

Tau pathology is known to spread in a hierarchical pattern in Alzheimer's disease (AD) brain during disease progression, likely by trans-synaptic tau transfer between neurons. However, the tau species involved in inter-neuron propagation remains unclear. To identify tau species responsible for...

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Autores principales: Takeda, Shuko, Wegmann, Susanne, Cho, Hansang, DeVos, Sarah L., Commins, Caitlin, Roe, Allyson D., Nicholls, Samantha B., Carlson, George A., Pitstick, Rose, Nobuhara, Chloe K., Costantino, Isabel, Frosch, Matthew P., Müller, Daniel J., Irimia, Daniel, Hyman, Bradley T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608380/
https://www.ncbi.nlm.nih.gov/pubmed/26458742
http://dx.doi.org/10.1038/ncomms9490
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author Takeda, Shuko
Wegmann, Susanne
Cho, Hansang
DeVos, Sarah L.
Commins, Caitlin
Roe, Allyson D.
Nicholls, Samantha B.
Carlson, George A.
Pitstick, Rose
Nobuhara, Chloe K.
Costantino, Isabel
Frosch, Matthew P.
Müller, Daniel J.
Irimia, Daniel
Hyman, Bradley T.
author_facet Takeda, Shuko
Wegmann, Susanne
Cho, Hansang
DeVos, Sarah L.
Commins, Caitlin
Roe, Allyson D.
Nicholls, Samantha B.
Carlson, George A.
Pitstick, Rose
Nobuhara, Chloe K.
Costantino, Isabel
Frosch, Matthew P.
Müller, Daniel J.
Irimia, Daniel
Hyman, Bradley T.
author_sort Takeda, Shuko
collection PubMed
description Tau pathology is known to spread in a hierarchical pattern in Alzheimer's disease (AD) brain during disease progression, likely by trans-synaptic tau transfer between neurons. However, the tau species involved in inter-neuron propagation remains unclear. To identify tau species responsible for propagation, we examined uptake and propagation properties of different tau species derived from postmortem cortical extracts and brain interstitial fluid of tau-transgenic mice, as well as human AD cortices. Here we show that PBS-soluble phosphorylated high-molecular-weight (HMW) tau, though very low in abundance, is taken up, axonally transported, and passed on to synaptically connected neurons. Our findings suggest that a rare species of soluble phosphorylated HMW tau is the endogenous form of tau involved in propagation and could be a target for therapeutic intervention and biomarker development.
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spelling pubmed-46083802015-11-25 Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain Takeda, Shuko Wegmann, Susanne Cho, Hansang DeVos, Sarah L. Commins, Caitlin Roe, Allyson D. Nicholls, Samantha B. Carlson, George A. Pitstick, Rose Nobuhara, Chloe K. Costantino, Isabel Frosch, Matthew P. Müller, Daniel J. Irimia, Daniel Hyman, Bradley T. Nat Commun Article Tau pathology is known to spread in a hierarchical pattern in Alzheimer's disease (AD) brain during disease progression, likely by trans-synaptic tau transfer between neurons. However, the tau species involved in inter-neuron propagation remains unclear. To identify tau species responsible for propagation, we examined uptake and propagation properties of different tau species derived from postmortem cortical extracts and brain interstitial fluid of tau-transgenic mice, as well as human AD cortices. Here we show that PBS-soluble phosphorylated high-molecular-weight (HMW) tau, though very low in abundance, is taken up, axonally transported, and passed on to synaptically connected neurons. Our findings suggest that a rare species of soluble phosphorylated HMW tau is the endogenous form of tau involved in propagation and could be a target for therapeutic intervention and biomarker development. Nature Pub. Group 2015-10-13 /pmc/articles/PMC4608380/ /pubmed/26458742 http://dx.doi.org/10.1038/ncomms9490 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Takeda, Shuko
Wegmann, Susanne
Cho, Hansang
DeVos, Sarah L.
Commins, Caitlin
Roe, Allyson D.
Nicholls, Samantha B.
Carlson, George A.
Pitstick, Rose
Nobuhara, Chloe K.
Costantino, Isabel
Frosch, Matthew P.
Müller, Daniel J.
Irimia, Daniel
Hyman, Bradley T.
Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain
title Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain
title_full Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain
title_fullStr Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain
title_full_unstemmed Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain
title_short Neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from Alzheimer's disease brain
title_sort neuronal uptake and propagation of a rare phosphorylated high-molecular-weight tau derived from alzheimer's disease brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608380/
https://www.ncbi.nlm.nih.gov/pubmed/26458742
http://dx.doi.org/10.1038/ncomms9490
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