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Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system
α-Synuclein and tau are abundant multifunctional brain proteins that are mainly expressed in the presynaptic and axonal compartments of neurons, respectively. Previous works have revealed that intracellular deposition of α-synuclein and/or tau causes many neurodegenerative disorders, including Alzhe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664117/ https://www.ncbi.nlm.nih.gov/pubmed/37843221 http://dx.doi.org/10.4103/1673-5374.382231 |
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author | Jin, Mingyue Wang, Shengming Gao, Xiaodie Zou, Zhenyou Hirotsune, Shinji Sun, Liyuan |
author_facet | Jin, Mingyue Wang, Shengming Gao, Xiaodie Zou, Zhenyou Hirotsune, Shinji Sun, Liyuan |
author_sort | Jin, Mingyue |
collection | PubMed |
description | α-Synuclein and tau are abundant multifunctional brain proteins that are mainly expressed in the presynaptic and axonal compartments of neurons, respectively. Previous works have revealed that intracellular deposition of α-synuclein and/or tau causes many neurodegenerative disorders, including Alzheimer’s disease and Parkinson’s disease. Despite intense investigation, the normal physiological functions and roles of α-synuclein and tau are still unclear, owing to the fact that mice with knockout of either of these proteins do not present apparent phenotypes. Interestingly, the co-occurrence of α-synuclein and tau aggregates was found in post-mortem brains with synucleinopathies and tauopathies, some of which share similarities in clinical manifestations. Furthermore, the direct interaction of α-synuclein with tau is considered to promote the fibrillization of each of the proteins in vitro and in vivo. On the other hand, our recent findings have revealed that α-synuclein and tau are cooperatively involved in brain development in a stage-dependent manner. These findings indicate strong cross-talk between the two proteins in physiology and pathology. In this review, we provide a summary of the recent findings on the functional roles of α-synuclein and tau in the physiological conditions and pathogenesis of neurodegenerative diseases. A deep understanding of the interplay between α-synuclein and tau in physiological and pathological conditions might provide novel targets for clinical diagnosis and therapeutic strategies to treat neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-10664117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-106641172023-09-04 Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system Jin, Mingyue Wang, Shengming Gao, Xiaodie Zou, Zhenyou Hirotsune, Shinji Sun, Liyuan Neural Regen Res Review α-Synuclein and tau are abundant multifunctional brain proteins that are mainly expressed in the presynaptic and axonal compartments of neurons, respectively. Previous works have revealed that intracellular deposition of α-synuclein and/or tau causes many neurodegenerative disorders, including Alzheimer’s disease and Parkinson’s disease. Despite intense investigation, the normal physiological functions and roles of α-synuclein and tau are still unclear, owing to the fact that mice with knockout of either of these proteins do not present apparent phenotypes. Interestingly, the co-occurrence of α-synuclein and tau aggregates was found in post-mortem brains with synucleinopathies and tauopathies, some of which share similarities in clinical manifestations. Furthermore, the direct interaction of α-synuclein with tau is considered to promote the fibrillization of each of the proteins in vitro and in vivo. On the other hand, our recent findings have revealed that α-synuclein and tau are cooperatively involved in brain development in a stage-dependent manner. These findings indicate strong cross-talk between the two proteins in physiology and pathology. In this review, we provide a summary of the recent findings on the functional roles of α-synuclein and tau in the physiological conditions and pathogenesis of neurodegenerative diseases. A deep understanding of the interplay between α-synuclein and tau in physiological and pathological conditions might provide novel targets for clinical diagnosis and therapeutic strategies to treat neurodegenerative diseases. Wolters Kluwer - Medknow 2023-09-04 /pmc/articles/PMC10664117/ /pubmed/37843221 http://dx.doi.org/10.4103/1673-5374.382231 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Jin, Mingyue Wang, Shengming Gao, Xiaodie Zou, Zhenyou Hirotsune, Shinji Sun, Liyuan Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
title | Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
title_full | Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
title_fullStr | Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
title_full_unstemmed | Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
title_short | Pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
title_sort | pathological and physiological functional cross-talks of α-synuclein and tau in the central nervous system |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664117/ https://www.ncbi.nlm.nih.gov/pubmed/37843221 http://dx.doi.org/10.4103/1673-5374.382231 |
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