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Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders

There is compelling evidence that a number of neurodegenerative diseases share common pathogenic mechanisms. Better understanding these mechanisms will allow us to develop new therapeutic strategies. This commentary follows up on our recent findings that tau pathology can be found in healthy fetal t...

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Detalles Bibliográficos
Autores principales: Maxan, Alexander, Cicchetti, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946355/
https://www.ncbi.nlm.nih.gov/pubmed/29760562
http://dx.doi.org/10.1177/1179069518772380
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author Maxan, Alexander
Cicchetti, Francesca
author_facet Maxan, Alexander
Cicchetti, Francesca
author_sort Maxan, Alexander
collection PubMed
description There is compelling evidence that a number of neurodegenerative diseases share common pathogenic mechanisms. Better understanding these mechanisms will allow us to develop new therapeutic strategies. This commentary follows up on our recent findings that tau pathology can be found in healthy fetal tissue transplanted into the brain of patients with either Huntington or Parkinson disease. We will examine how tau appears to be shared in a number of different conditions and how its expression relates to cognitive decline and disease progression. We will further review pathogenic mechanisms and especially the relevance of the possible prion-like behavior of tau. We will conclude by discussing how all this work opens up novel therapeutic approaches to treating the cognitive impairments related to neurodegenerative diseases using a common strategy.
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spelling pubmed-59463552018-05-14 Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders Maxan, Alexander Cicchetti, Francesca J Exp Neurosci Commentary There is compelling evidence that a number of neurodegenerative diseases share common pathogenic mechanisms. Better understanding these mechanisms will allow us to develop new therapeutic strategies. This commentary follows up on our recent findings that tau pathology can be found in healthy fetal tissue transplanted into the brain of patients with either Huntington or Parkinson disease. We will examine how tau appears to be shared in a number of different conditions and how its expression relates to cognitive decline and disease progression. We will further review pathogenic mechanisms and especially the relevance of the possible prion-like behavior of tau. We will conclude by discussing how all this work opens up novel therapeutic approaches to treating the cognitive impairments related to neurodegenerative diseases using a common strategy. SAGE Publications 2018-05-01 /pmc/articles/PMC5946355/ /pubmed/29760562 http://dx.doi.org/10.1177/1179069518772380 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Commentary
Maxan, Alexander
Cicchetti, Francesca
Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders
title Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders
title_full Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders
title_fullStr Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders
title_full_unstemmed Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders
title_short Tau: A Common Denominator and Therapeutic Target for Neurodegenerative Disorders
title_sort tau: a common denominator and therapeutic target for neurodegenerative disorders
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946355/
https://www.ncbi.nlm.nih.gov/pubmed/29760562
http://dx.doi.org/10.1177/1179069518772380
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