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Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke
Mitochondrial autophagy is an early defense and protection process that selectively clears dysfunctional or excessive mitochondria through a distinctive mechanism to maintain intracellular homeostasis. Mitochondrial dysfunction during cerebral stroke involves metabolic disbalance, oxidative stress,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319822/ https://www.ncbi.nlm.nih.gov/pubmed/34335233 http://dx.doi.org/10.3389/fnagi.2021.698601 |
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author | Lei, Li Yang, Shuaifeng Lu, Xiaoyang Zhang, Yongfa Li, Tao |
author_facet | Lei, Li Yang, Shuaifeng Lu, Xiaoyang Zhang, Yongfa Li, Tao |
author_sort | Lei, Li |
collection | PubMed |
description | Mitochondrial autophagy is an early defense and protection process that selectively clears dysfunctional or excessive mitochondria through a distinctive mechanism to maintain intracellular homeostasis. Mitochondrial dysfunction during cerebral stroke involves metabolic disbalance, oxidative stress, apoptosis, endoplasmic reticulum stress, and abnormal mitochondrial autophagy. This article reviews the research progress on the mechanism of mitochondrial autophagy in ischemic stroke to provide a theoretical basis for further research on mitochondrial autophagy and the treatment of ischemic stroke. |
format | Online Article Text |
id | pubmed-8319822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83198222021-07-30 Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke Lei, Li Yang, Shuaifeng Lu, Xiaoyang Zhang, Yongfa Li, Tao Front Aging Neurosci Neuroscience Mitochondrial autophagy is an early defense and protection process that selectively clears dysfunctional or excessive mitochondria through a distinctive mechanism to maintain intracellular homeostasis. Mitochondrial dysfunction during cerebral stroke involves metabolic disbalance, oxidative stress, apoptosis, endoplasmic reticulum stress, and abnormal mitochondrial autophagy. This article reviews the research progress on the mechanism of mitochondrial autophagy in ischemic stroke to provide a theoretical basis for further research on mitochondrial autophagy and the treatment of ischemic stroke. Frontiers Media S.A. 2021-07-15 /pmc/articles/PMC8319822/ /pubmed/34335233 http://dx.doi.org/10.3389/fnagi.2021.698601 Text en Copyright © 2021 Lei, Yang, Lu, Zhang and Li. 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 Lei, Li Yang, Shuaifeng Lu, Xiaoyang Zhang, Yongfa Li, Tao Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke |
title | Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke |
title_full | Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke |
title_fullStr | Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke |
title_full_unstemmed | Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke |
title_short | Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke |
title_sort | research progress on the mechanism of mitochondrial autophagy in cerebral stroke |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319822/ https://www.ncbi.nlm.nih.gov/pubmed/34335233 http://dx.doi.org/10.3389/fnagi.2021.698601 |
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