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Tau Seeding Mouse Models with Patient Brain-Derived Aggregates

Tauopathies are a heterogeneous class of neurodegenerative diseases characterized by intracellular inclusions of aggregated tau proteins. Tau aggregates in different tauopathies have distinct structural features and can be found in different cell types. Transgenic animal models overexpressing human...

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Detalles Bibliográficos
Autores principales: Robert, Aiko, Schöll, Michael, Vogels, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201271/
https://www.ncbi.nlm.nih.gov/pubmed/34200180
http://dx.doi.org/10.3390/ijms22116132
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author Robert, Aiko
Schöll, Michael
Vogels, Thomas
author_facet Robert, Aiko
Schöll, Michael
Vogels, Thomas
author_sort Robert, Aiko
collection PubMed
description Tauopathies are a heterogeneous class of neurodegenerative diseases characterized by intracellular inclusions of aggregated tau proteins. Tau aggregates in different tauopathies have distinct structural features and can be found in different cell types. Transgenic animal models overexpressing human tau have been used for over two decades in the research of tau pathology. However, these models poorly recapitulate the heterogeneity of tauopathies found in human brains. Recent findings demonstrate that injection of purified tau aggregates from the brains of human tauopathy patients recapitulates both the structural features and cell-type specificity of the tau pathology of the donor tauopathy. These models may therefore have unique translational value in the study of functional consequences of tau pathology, tau-based diagnostics, and tau targeting therapeutics. This review provides an update of the literature relating to seeding-based tauopathy and their potential applications.
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spelling pubmed-82012712021-06-15 Tau Seeding Mouse Models with Patient Brain-Derived Aggregates Robert, Aiko Schöll, Michael Vogels, Thomas Int J Mol Sci Review Tauopathies are a heterogeneous class of neurodegenerative diseases characterized by intracellular inclusions of aggregated tau proteins. Tau aggregates in different tauopathies have distinct structural features and can be found in different cell types. Transgenic animal models overexpressing human tau have been used for over two decades in the research of tau pathology. However, these models poorly recapitulate the heterogeneity of tauopathies found in human brains. Recent findings demonstrate that injection of purified tau aggregates from the brains of human tauopathy patients recapitulates both the structural features and cell-type specificity of the tau pathology of the donor tauopathy. These models may therefore have unique translational value in the study of functional consequences of tau pathology, tau-based diagnostics, and tau targeting therapeutics. This review provides an update of the literature relating to seeding-based tauopathy and their potential applications. MDPI 2021-06-07 /pmc/articles/PMC8201271/ /pubmed/34200180 http://dx.doi.org/10.3390/ijms22116132 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Robert, Aiko
Schöll, Michael
Vogels, Thomas
Tau Seeding Mouse Models with Patient Brain-Derived Aggregates
title Tau Seeding Mouse Models with Patient Brain-Derived Aggregates
title_full Tau Seeding Mouse Models with Patient Brain-Derived Aggregates
title_fullStr Tau Seeding Mouse Models with Patient Brain-Derived Aggregates
title_full_unstemmed Tau Seeding Mouse Models with Patient Brain-Derived Aggregates
title_short Tau Seeding Mouse Models with Patient Brain-Derived Aggregates
title_sort tau seeding mouse models with patient brain-derived aggregates
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201271/
https://www.ncbi.nlm.nih.gov/pubmed/34200180
http://dx.doi.org/10.3390/ijms22116132
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