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Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults
Neurons rely heavily on mitochondria for their function and survival. Mitochondrial dysfunction contributes to the pathogenesis of neurodegenerative diseases such as Parkinson's disease. PGC-1α is a master regulator of mitochondrial biogenesis and function. Here we identify necdin as a potent P...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793078/ https://www.ncbi.nlm.nih.gov/pubmed/26971449 http://dx.doi.org/10.1038/ncomms10943 |
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author | Hasegawa, Koichi Yasuda, Toru Shiraishi, Chinatsu Fujiwara, Kazushiro Przedborski, Serge Mochizuki, Hideki Yoshikawa, Kazuaki |
author_facet | Hasegawa, Koichi Yasuda, Toru Shiraishi, Chinatsu Fujiwara, Kazushiro Przedborski, Serge Mochizuki, Hideki Yoshikawa, Kazuaki |
author_sort | Hasegawa, Koichi |
collection | PubMed |
description | Neurons rely heavily on mitochondria for their function and survival. Mitochondrial dysfunction contributes to the pathogenesis of neurodegenerative diseases such as Parkinson's disease. PGC-1α is a master regulator of mitochondrial biogenesis and function. Here we identify necdin as a potent PGC-1α stabilizer that promotes mitochondrial biogenesis via PGC-1α in mammalian neurons. Expression of genes encoding mitochondria-specific proteins decreases significantly in necdin-null cortical neurons, where mitochondrial function and expression of the PGC-1α protein are reduced. Necdin strongly stabilizes PGC-1α by inhibiting its ubiquitin-dependent degradation. Forced expression of necdin enhances mitochondrial function in primary cortical neurons and human SH-SY5Y neuroblastoma cells to prevent mitochondrial respiratory chain inhibitor-induced degeneration. Moreover, overexpression of necdin in the substantia nigra in vivo of adult mice protects dopaminergic neurons against degeneration in experimental Parkinson's disease. These data reveal that necdin promotes mitochondrial biogenesis through stabilization of endogenous PGC-1α to exert neuroprotection against mitochondrial insults. |
format | Online Article Text |
id | pubmed-4793078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47930782016-03-21 Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults Hasegawa, Koichi Yasuda, Toru Shiraishi, Chinatsu Fujiwara, Kazushiro Przedborski, Serge Mochizuki, Hideki Yoshikawa, Kazuaki Nat Commun Article Neurons rely heavily on mitochondria for their function and survival. Mitochondrial dysfunction contributes to the pathogenesis of neurodegenerative diseases such as Parkinson's disease. PGC-1α is a master regulator of mitochondrial biogenesis and function. Here we identify necdin as a potent PGC-1α stabilizer that promotes mitochondrial biogenesis via PGC-1α in mammalian neurons. Expression of genes encoding mitochondria-specific proteins decreases significantly in necdin-null cortical neurons, where mitochondrial function and expression of the PGC-1α protein are reduced. Necdin strongly stabilizes PGC-1α by inhibiting its ubiquitin-dependent degradation. Forced expression of necdin enhances mitochondrial function in primary cortical neurons and human SH-SY5Y neuroblastoma cells to prevent mitochondrial respiratory chain inhibitor-induced degeneration. Moreover, overexpression of necdin in the substantia nigra in vivo of adult mice protects dopaminergic neurons against degeneration in experimental Parkinson's disease. These data reveal that necdin promotes mitochondrial biogenesis through stabilization of endogenous PGC-1α to exert neuroprotection against mitochondrial insults. Nature Publishing Group 2016-03-14 /pmc/articles/PMC4793078/ /pubmed/26971449 http://dx.doi.org/10.1038/ncomms10943 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hasegawa, Koichi Yasuda, Toru Shiraishi, Chinatsu Fujiwara, Kazushiro Przedborski, Serge Mochizuki, Hideki Yoshikawa, Kazuaki Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
title | Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
title_full | Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
title_fullStr | Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
title_full_unstemmed | Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
title_short | Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
title_sort | promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793078/ https://www.ncbi.nlm.nih.gov/pubmed/26971449 http://dx.doi.org/10.1038/ncomms10943 |
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