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Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review

Background: Parkin-mediated mitophagy is the dominant mitophagy pathway of neural cells. Its restoration will result in prevention of cognitive decline, including Alzheimer's disease (AD). The role of this mitophagy pathway in neurodegenerative diseases has drawn attention in recent years. The...

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Autores principales: Goudarzi, Sepideh, Hosseini, Asieh, Abdollahi, Mohammad, Haghi-Aminjan, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358451/
https://www.ncbi.nlm.nih.gov/pubmed/34393755
http://dx.doi.org/10.3389/fnagi.2021.674071
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author Goudarzi, Sepideh
Hosseini, Asieh
Abdollahi, Mohammad
Haghi-Aminjan, Hamed
author_facet Goudarzi, Sepideh
Hosseini, Asieh
Abdollahi, Mohammad
Haghi-Aminjan, Hamed
author_sort Goudarzi, Sepideh
collection PubMed
description Background: Parkin-mediated mitophagy is the dominant mitophagy pathway of neural cells. Its restoration will result in prevention of cognitive decline, including Alzheimer's disease (AD). The role of this mitophagy pathway in neurodegenerative diseases has drawn attention in recent years. The two main pathological proteins in AD, amyloid β (Aβ) and human Tau (hTau), interfere with mitochondrial dynamics through several pathways. However, taking into consideration the specific interactions between Aβ/hTau and Parkin, special focus is required on this mitophagy pathway and AD. In this review, these interactions are fully discussed, and an overview of the neuroprotective drugs that enhance Parkin-mediated mitophagy is presented. Methods: This systematic review was performed according to PRISMA guidelines, and a comprehensive literature search was done in the electronic databases up to September 2020, using search terms in the titles and abstracts to identify relevant studies. One hundred eighty-six articles were found, and 113 articles were screened by title and abstract. Finally, 25 articles were included in this systematic review according to our inclusion and exclusion criteria. Results: Accumulation of Aβ and hTau affects mitophagy, including Parkin-mediated. Tau seems to prevent Parkin translocation directly. A Parkin level in the cell appears to be of importance in determining the damage caused by Aβ and hTau and in the future therapeutic approaches. Parkin controls the PINK1 level via the presenillins, suggesting that mutations in presenillins affect Parkin mitophagy. Significance: Parkin mitophagy is a process affected by several AD pathological events multidimensionally.
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spelling pubmed-83584512021-08-13 Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review Goudarzi, Sepideh Hosseini, Asieh Abdollahi, Mohammad Haghi-Aminjan, Hamed Front Aging Neurosci Neuroscience Background: Parkin-mediated mitophagy is the dominant mitophagy pathway of neural cells. Its restoration will result in prevention of cognitive decline, including Alzheimer's disease (AD). The role of this mitophagy pathway in neurodegenerative diseases has drawn attention in recent years. The two main pathological proteins in AD, amyloid β (Aβ) and human Tau (hTau), interfere with mitochondrial dynamics through several pathways. However, taking into consideration the specific interactions between Aβ/hTau and Parkin, special focus is required on this mitophagy pathway and AD. In this review, these interactions are fully discussed, and an overview of the neuroprotective drugs that enhance Parkin-mediated mitophagy is presented. Methods: This systematic review was performed according to PRISMA guidelines, and a comprehensive literature search was done in the electronic databases up to September 2020, using search terms in the titles and abstracts to identify relevant studies. One hundred eighty-six articles were found, and 113 articles were screened by title and abstract. Finally, 25 articles were included in this systematic review according to our inclusion and exclusion criteria. Results: Accumulation of Aβ and hTau affects mitophagy, including Parkin-mediated. Tau seems to prevent Parkin translocation directly. A Parkin level in the cell appears to be of importance in determining the damage caused by Aβ and hTau and in the future therapeutic approaches. Parkin controls the PINK1 level via the presenillins, suggesting that mutations in presenillins affect Parkin mitophagy. Significance: Parkin mitophagy is a process affected by several AD pathological events multidimensionally. Frontiers Media S.A. 2021-07-29 /pmc/articles/PMC8358451/ /pubmed/34393755 http://dx.doi.org/10.3389/fnagi.2021.674071 Text en Copyright © 2021 Goudarzi, Hosseini, Abdollahi and Haghi-Aminjan. 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
Goudarzi, Sepideh
Hosseini, Asieh
Abdollahi, Mohammad
Haghi-Aminjan, Hamed
Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review
title Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review
title_full Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review
title_fullStr Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review
title_full_unstemmed Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review
title_short Insights Into Parkin-Mediated Mitophagy in Alzheimer's Disease: A Systematic Review
title_sort insights into parkin-mediated mitophagy in alzheimer's disease: a systematic review
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358451/
https://www.ncbi.nlm.nih.gov/pubmed/34393755
http://dx.doi.org/10.3389/fnagi.2021.674071
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