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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...

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Autores principales: Hasegawa, Koichi, Yasuda, Toru, Shiraishi, Chinatsu, Fujiwara, Kazushiro, Przedborski, Serge, Mochizuki, Hideki, Yoshikawa, Kazuaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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