The mitochondrial UPR: mechanisms, physiological functions and implications in ageing
Top Cited Papers
- 22 November 2017
- journal article
- review article
- Published by Springer Nature in Nature Reviews Molecular Cell Biology
- Vol. 19 (2), 109-120
- https://doi.org/10.1038/nrm.2017.110
Abstract
Mitochondrial function declines during ageing owing to the accumulation of deleterious mitochondrial genomes and damage resulting from the localized generation of reactive oxygen species, both of which are often exacerbated in diseases such as Parkinson disease. Cells have several mechanisms to assess mitochondrial function and activate a transcriptional response known as the mitochondrial unfolded protein response (UPRmt) when mitochondrial integrity and function are impaired. The UPRmt promotes cell survival and the recovery of the mitochondrial network to ensure optimal cellular function. Recent insights into the regulation, mechanisms and functions of the UPRmt have uncovered important and complex links to ageing and ageing-associated diseases. In this Review, we discuss the signal transduction mechanisms that regulate the UPRmt and the physiological consequences of its activation that affect cellular and organismal health during ageing.This publication has 150 references indexed in Scilit:
- Mitonuclear protein imbalance as a conserved longevity mechanismNature, 2013
- Transcription factor ATF5 is required for terminal differentiation and survival of olfactory sensory neuronsProceedings of the National Academy of Sciences, 2012
- Step-Wise Methylation of Histone H3K9 Positions Heterochromatin at the Nuclear PeripheryCell, 2012
- Inactivation of Conserved C. elegans Genes Engages Pathogen- and Xenobiotic-Associated DefensesCell, 2012
- The Cell-Non-Autonomous Nature of Electron Transport Chain-Mediated LongevityCell, 2011
- Inhibition of Respiration Extends C. elegans Life Span via Reactive Oxygen Species that Increase HIF-1 ActivityCurrent Biology, 2010
- Parkin overexpression selects against a deleterious mtDNA mutation in heteroplasmic cybrid cellsProceedings of the National Academy of Sciences, 2010
- The Matrix Peptide Exporter HAF-1 Signals a Mitochondrial UPR by Activating the Transcription Factor ZC376.7 in C. elegansMolecular Cell, 2010
- PINK1-dependent recruitment of Parkin to mitochondria in mitophagyProceedings of the National Academy of Sciences, 2009
- An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative StressMolecular Cell, 2003