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Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration

Endoplasmic reticulum–mitochondria contact sites (ERMCSs) are dynamic contact regions with a distance of 10–30 nm between the endoplasmic reticulum and mitochondria. Endoplasmic reticulum–mitochondria contact sites regulate various biological processes, including lipid transfer, calcium homeostasis,...

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Detalles Bibliográficos
Autores principales: Xu, Lingna, Wang, Xi, Tong, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314981/
https://www.ncbi.nlm.nih.gov/pubmed/32626703
http://dx.doi.org/10.3389/fcell.2020.00428
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author Xu, Lingna
Wang, Xi
Tong, Chao
author_facet Xu, Lingna
Wang, Xi
Tong, Chao
author_sort Xu, Lingna
collection PubMed
description Endoplasmic reticulum–mitochondria contact sites (ERMCSs) are dynamic contact regions with a distance of 10–30 nm between the endoplasmic reticulum and mitochondria. Endoplasmic reticulum–mitochondria contact sites regulate various biological processes, including lipid transfer, calcium homeostasis, autophagy, and mitochondrial dynamics. The dysfunction of ERMCS is closely associated with various neurodegenerative diseases, including Parkinson’s disease, Alzheimer’s disease, and amyotrophic lateral sclerosis. In this review, we will summarize the current knowledge of the components and organization of ERMCSs, the methods for monitoring ERMCSs, and the physiological functions of ERMCSs in different model systems. Additionally, we will emphasize the current understanding of the malfunction of ERMCSs and their potential roles in neurodegenerative diseases.
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spelling pubmed-73149812020-07-02 Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration Xu, Lingna Wang, Xi Tong, Chao Front Cell Dev Biol Cell and Developmental Biology Endoplasmic reticulum–mitochondria contact sites (ERMCSs) are dynamic contact regions with a distance of 10–30 nm between the endoplasmic reticulum and mitochondria. Endoplasmic reticulum–mitochondria contact sites regulate various biological processes, including lipid transfer, calcium homeostasis, autophagy, and mitochondrial dynamics. The dysfunction of ERMCS is closely associated with various neurodegenerative diseases, including Parkinson’s disease, Alzheimer’s disease, and amyotrophic lateral sclerosis. In this review, we will summarize the current knowledge of the components and organization of ERMCSs, the methods for monitoring ERMCSs, and the physiological functions of ERMCSs in different model systems. Additionally, we will emphasize the current understanding of the malfunction of ERMCSs and their potential roles in neurodegenerative diseases. Frontiers Media S.A. 2020-06-18 /pmc/articles/PMC7314981/ /pubmed/32626703 http://dx.doi.org/10.3389/fcell.2020.00428 Text en Copyright © 2020 Xu, Wang and Tong. http://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 Cell and Developmental Biology
Xu, Lingna
Wang, Xi
Tong, Chao
Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration
title Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration
title_full Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration
title_fullStr Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration
title_full_unstemmed Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration
title_short Endoplasmic Reticulum–Mitochondria Contact Sites and Neurodegeneration
title_sort endoplasmic reticulum–mitochondria contact sites and neurodegeneration
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314981/
https://www.ncbi.nlm.nih.gov/pubmed/32626703
http://dx.doi.org/10.3389/fcell.2020.00428
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