Alleviation of neuronal energy deficiency by mTOR inhibition as a treatment for mitochondria-related neurodegeneration

Bibliographic Details
Title: Alleviation of neuronal energy deficiency by mTOR inhibition as a treatment for mitochondria-related neurodegeneration
Authors: Xinde Zheng, Leah Boyer, Mingji Jin, Yongsung Kim, Weiwei Fan, Cedric Bardy, Travis Berggren, Ronald M Evans, Fred H Gage, Tony Hunter
Source: eLife, Vol 5 (2016)
Publisher Information: eLife Sciences Publications Ltd, 2016.
Publication Year: 2016
Collection: LCC:Medicine
LCC:Science
LCC:Biology (General)
Subject Terms: mitochondria, rapamycin, ATP, iPS disease modeling, maternally inherited Leigh syndrome, Medicine, Science, Biology (General), QH301-705.5
More Details: mTOR inhibition is beneficial in neurodegenerative disease models and its effects are often attributable to the modulation of autophagy and anti-apoptosis. Here, we report a neglected but important bioenergetic effect of mTOR inhibition in neurons. mTOR inhibition by rapamycin significantly preserves neuronal ATP levels, particularly when oxidative phosphorylation is impaired, such as in neurons treated with mitochondrial inhibitors, or in neurons derived from maternally inherited Leigh syndrome (MILS) patient iPS cells with ATP synthase deficiency. Rapamycin treatment significantly improves the resistance of MILS neurons to glutamate toxicity. Surprisingly, in mitochondrially defective neurons, but not neuroprogenitor cells, ribosomal S6 and S6 kinase phosphorylation increased over time, despite activation of AMPK, which is often linked to mTOR inhibition. A rapamycin-induced decrease in protein synthesis, a major energy-consuming process, may account for its ATP-saving effect. We propose that a mild reduction in protein synthesis may have the potential to treat mitochondria-related neurodegeneration.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2050-084X
Relation: https://elifesciences.org/articles/13378; https://doaj.org/toc/2050-084X
DOI: 10.7554/eLife.13378
Access URL: https://doaj.org/article/33701fc01b264587a4c9be099cc54e22
Accession Number: edsdoj.33701fc01b264587a4c9be099cc54e22
Database: Directory of Open Access Journals
More Details
ISSN:2050084X
DOI:10.7554/eLife.13378
Published in:eLife
Language:English