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Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice

Tau is a microtubule stabilizing protein that forms aggregates in Alzheimer’s disease (AD). Tau derived from AD patients’ brains induces tau aggregation in a prion-like manner when injected into susceptible mouse models. Here we investigated whether cerebrospinal fluid (CSF) collected from patients...

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Autores principales: Skachokova, Zhiva, Martinisi, Alfonso, Flach, Martin, Sprenger, Frederik, Naegelin, Yvonne, Steiner-Monard, Viviane, Sollberger, Marc, Monsch, Andreas U., Goedert, Michel, Tolnay, Markus, Winkler, David T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503541/
https://www.ncbi.nlm.nih.gov/pubmed/31064413
http://dx.doi.org/10.1186/s40478-019-0725-3
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author Skachokova, Zhiva
Martinisi, Alfonso
Flach, Martin
Sprenger, Frederik
Naegelin, Yvonne
Steiner-Monard, Viviane
Sollberger, Marc
Monsch, Andreas U.
Goedert, Michel
Tolnay, Markus
Winkler, David T.
author_facet Skachokova, Zhiva
Martinisi, Alfonso
Flach, Martin
Sprenger, Frederik
Naegelin, Yvonne
Steiner-Monard, Viviane
Sollberger, Marc
Monsch, Andreas U.
Goedert, Michel
Tolnay, Markus
Winkler, David T.
author_sort Skachokova, Zhiva
collection PubMed
description Tau is a microtubule stabilizing protein that forms aggregates in Alzheimer’s disease (AD). Tau derived from AD patients’ brains induces tau aggregation in a prion-like manner when injected into susceptible mouse models. Here we investigated whether cerebrospinal fluid (CSF) collected from patients diagnosed with probable AD or mild cognitive impairment (MCI) likely due to AD harbors a prion-like tau seeding potential. CSF was injected intrahippocampally into young P301S tau transgenic mice. CSF obtained from AD or MCI patients increased hippocampal tau hyperphosphorylation and tau tangle formation in these mice at 4 months post-seeding. Tau pathology was also accentuated in the contralateral hippocampus, and in anterior and posterior directions, indicative of spreading. We provide first evidence for in vivo prion-like properties of AD patients’ CSF, accelerating tau pathology in susceptible tau transgenic mice. This demonstrates that biologically active tau seeds reach the CSF compartment in AD. Further studies may help to evaluate strain specific properties of CSF derived tau bioseeds, and to assess their diagnostic potential. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-019-0725-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-65035412019-05-10 Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice Skachokova, Zhiva Martinisi, Alfonso Flach, Martin Sprenger, Frederik Naegelin, Yvonne Steiner-Monard, Viviane Sollberger, Marc Monsch, Andreas U. Goedert, Michel Tolnay, Markus Winkler, David T. Acta Neuropathol Commun Research Tau is a microtubule stabilizing protein that forms aggregates in Alzheimer’s disease (AD). Tau derived from AD patients’ brains induces tau aggregation in a prion-like manner when injected into susceptible mouse models. Here we investigated whether cerebrospinal fluid (CSF) collected from patients diagnosed with probable AD or mild cognitive impairment (MCI) likely due to AD harbors a prion-like tau seeding potential. CSF was injected intrahippocampally into young P301S tau transgenic mice. CSF obtained from AD or MCI patients increased hippocampal tau hyperphosphorylation and tau tangle formation in these mice at 4 months post-seeding. Tau pathology was also accentuated in the contralateral hippocampus, and in anterior and posterior directions, indicative of spreading. We provide first evidence for in vivo prion-like properties of AD patients’ CSF, accelerating tau pathology in susceptible tau transgenic mice. This demonstrates that biologically active tau seeds reach the CSF compartment in AD. Further studies may help to evaluate strain specific properties of CSF derived tau bioseeds, and to assess their diagnostic potential. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-019-0725-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-07 /pmc/articles/PMC6503541/ /pubmed/31064413 http://dx.doi.org/10.1186/s40478-019-0725-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Skachokova, Zhiva
Martinisi, Alfonso
Flach, Martin
Sprenger, Frederik
Naegelin, Yvonne
Steiner-Monard, Viviane
Sollberger, Marc
Monsch, Andreas U.
Goedert, Michel
Tolnay, Markus
Winkler, David T.
Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
title Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
title_full Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
title_fullStr Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
title_full_unstemmed Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
title_short Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
title_sort cerebrospinal fluid from alzheimer’s disease patients promotes tau aggregation in transgenic mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503541/
https://www.ncbi.nlm.nih.gov/pubmed/31064413
http://dx.doi.org/10.1186/s40478-019-0725-3
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