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Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease

Parkinson’s disease (PD) is the second most common neurodegenerative disorder after Alzheimer’s disease. It is a chronic and progressive disorder estimated to affect at least 4 million people worldwide. Although the etiology of PD remains unclear, it has been found that the dysfunction of synaptic v...

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Detalles Bibliográficos
Autores principales: Zou, Li, Tian, Ye, Zhang, Zhentao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172812/
https://www.ncbi.nlm.nih.gov/pubmed/34093144
http://dx.doi.org/10.3389/fnint.2021.619160
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author Zou, Li
Tian, Ye
Zhang, Zhentao
author_facet Zou, Li
Tian, Ye
Zhang, Zhentao
author_sort Zou, Li
collection PubMed
description Parkinson’s disease (PD) is the second most common neurodegenerative disorder after Alzheimer’s disease. It is a chronic and progressive disorder estimated to affect at least 4 million people worldwide. Although the etiology of PD remains unclear, it has been found that the dysfunction of synaptic vesicle endocytosis (SVE) in neural terminal happens before the loss of dopaminergic neurons. Recently, accumulating evidence reveals that the PD-linked synaptic genes, including DNAJC6, SYNJ1, and SH3GL2, significantly contribute to the disruptions of SVE, which is vital for the pathogenesis of PD. In addition, the proteins encoded by other PD-associated genes such as SNCA, LRRK2, PRKN, and DJ-1 also play key roles in the regulation of SVE. Here we present the facts about SVE-related genes and discussed their potential relevance to the pathogenesis of PD.
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spelling pubmed-81728122021-06-04 Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease Zou, Li Tian, Ye Zhang, Zhentao Front Integr Neurosci Neuroscience Parkinson’s disease (PD) is the second most common neurodegenerative disorder after Alzheimer’s disease. It is a chronic and progressive disorder estimated to affect at least 4 million people worldwide. Although the etiology of PD remains unclear, it has been found that the dysfunction of synaptic vesicle endocytosis (SVE) in neural terminal happens before the loss of dopaminergic neurons. Recently, accumulating evidence reveals that the PD-linked synaptic genes, including DNAJC6, SYNJ1, and SH3GL2, significantly contribute to the disruptions of SVE, which is vital for the pathogenesis of PD. In addition, the proteins encoded by other PD-associated genes such as SNCA, LRRK2, PRKN, and DJ-1 also play key roles in the regulation of SVE. Here we present the facts about SVE-related genes and discussed their potential relevance to the pathogenesis of PD. Frontiers Media S.A. 2021-05-20 /pmc/articles/PMC8172812/ /pubmed/34093144 http://dx.doi.org/10.3389/fnint.2021.619160 Text en Copyright © 2021 Zou, Tian and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Zou, Li
Tian, Ye
Zhang, Zhentao
Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease
title Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease
title_full Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease
title_fullStr Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease
title_full_unstemmed Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease
title_short Dysfunction of Synaptic Vesicle Endocytosis in Parkinson’s Disease
title_sort dysfunction of synaptic vesicle endocytosis in parkinson’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172812/
https://www.ncbi.nlm.nih.gov/pubmed/34093144
http://dx.doi.org/10.3389/fnint.2021.619160
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