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Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures

Tau aggregation and hyperphosphorylation is a key neuropathological hallmark of Alzheimer's disease (AD), and the temporospatial spread of Tau observed during clinical manifestation suggests that Tau pathology may spread along the axonal network and propagate between synaptically connected neur...

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Autores principales: Katsikoudi, Antigoni, Ficulle, Elena, Cavallini, Annalisa, Sharman, Gary, Guyot, Amelie, Zagnoni, Michele, Eastwood, Brian J., Hutton, Michael, Bose, Suchira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489902/
https://www.ncbi.nlm.nih.gov/pubmed/32699110
http://dx.doi.org/10.1074/jbc.RA120.013325
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author Katsikoudi, Antigoni
Ficulle, Elena
Cavallini, Annalisa
Sharman, Gary
Guyot, Amelie
Zagnoni, Michele
Eastwood, Brian J.
Hutton, Michael
Bose, Suchira
author_facet Katsikoudi, Antigoni
Ficulle, Elena
Cavallini, Annalisa
Sharman, Gary
Guyot, Amelie
Zagnoni, Michele
Eastwood, Brian J.
Hutton, Michael
Bose, Suchira
author_sort Katsikoudi, Antigoni
collection PubMed
description Tau aggregation and hyperphosphorylation is a key neuropathological hallmark of Alzheimer's disease (AD), and the temporospatial spread of Tau observed during clinical manifestation suggests that Tau pathology may spread along the axonal network and propagate between synaptically connected neurons. Here, we have developed a cellular model that allows the study of human AD-derived Tau propagation from neuron to neuron using microfluidic devices. We show by using high-content imaging techniques and an in-house developed interactive computer program that human AD-derived Tau seeds rodent Tau that propagates trans-neuronally in a quantifiable manner in a microfluidic culture model. Moreover, we were able to convert this model to a medium-throughput format allowing the user to handle 16 two-chamber devices simultaneously in the footprint of a standard 96-well plate. Furthermore, we show that a small molecule inhibitor of aggregation can block the trans-neuronal transfer of Tau aggregates, suggesting that the system can be used to evaluate mechanisms of Tau transfer and find therapeutic interventions.
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spelling pubmed-74899022020-09-22 Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures Katsikoudi, Antigoni Ficulle, Elena Cavallini, Annalisa Sharman, Gary Guyot, Amelie Zagnoni, Michele Eastwood, Brian J. Hutton, Michael Bose, Suchira J Biol Chem Neurobiology Tau aggregation and hyperphosphorylation is a key neuropathological hallmark of Alzheimer's disease (AD), and the temporospatial spread of Tau observed during clinical manifestation suggests that Tau pathology may spread along the axonal network and propagate between synaptically connected neurons. Here, we have developed a cellular model that allows the study of human AD-derived Tau propagation from neuron to neuron using microfluidic devices. We show by using high-content imaging techniques and an in-house developed interactive computer program that human AD-derived Tau seeds rodent Tau that propagates trans-neuronally in a quantifiable manner in a microfluidic culture model. Moreover, we were able to convert this model to a medium-throughput format allowing the user to handle 16 two-chamber devices simultaneously in the footprint of a standard 96-well plate. Furthermore, we show that a small molecule inhibitor of aggregation can block the trans-neuronal transfer of Tau aggregates, suggesting that the system can be used to evaluate mechanisms of Tau transfer and find therapeutic interventions. American Society for Biochemistry and Molecular Biology 2020-09-11 2020-07-22 /pmc/articles/PMC7489902/ /pubmed/32699110 http://dx.doi.org/10.1074/jbc.RA120.013325 Text en © 2020 Katsikoudi et al. Author's Choice—Final version open access under the terms of the Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) .
spellingShingle Neurobiology
Katsikoudi, Antigoni
Ficulle, Elena
Cavallini, Annalisa
Sharman, Gary
Guyot, Amelie
Zagnoni, Michele
Eastwood, Brian J.
Hutton, Michael
Bose, Suchira
Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures
title Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures
title_full Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures
title_fullStr Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures
title_full_unstemmed Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures
title_short Quantitative propagation of assembled human Tau from Alzheimer's disease brain in microfluidic neuronal cultures
title_sort quantitative propagation of assembled human tau from alzheimer's disease brain in microfluidic neuronal cultures
topic Neurobiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489902/
https://www.ncbi.nlm.nih.gov/pubmed/32699110
http://dx.doi.org/10.1074/jbc.RA120.013325
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