The mitochondrial UPR: Mechanisms, physiological functions and implications in ageing

Tomer Shpilka, Cole M. Haynes*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

465 Scopus citations

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 (UPR(mt)) when mitochondrial integrity and function are impaired. The UPR(mt) 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 UPR(mt) have uncovered important and complex links to ageing and ageing-associated diseases. In this Review, we discuss the signal transduction mechanisms that regulate the UPR(mt) and the physiological consequences of its activation that affect cellular and organismal health during ageing.

Original languageEnglish
Pages (from-to)109-120
Number of pages12
JournalNature Reviews Molecular Cell Biology
Volume19
Issue number2
DOIs
StatePublished - 23 Jan 2018
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2018 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.

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