MitoTimer: a Novel Protein for Monitoring Mitochondrial Turnover in the Heart

Overview

Journal J Mol Med (Berl)

Specialty General Medicine

Date 2014 Dec 7

PMID 25479961

Citations 31

Authors

Roberta A Gottlieb

Aleksandr Stotland

Affiliations

Soon will be listed here.

Abstract

Mitochondrial quality control refers to the coordinated cellular systems involved in maintaining a population of healthy mitochondria. In addition to mitochondrial protein chaperones (Hsp10, Hsp60, and others) and proteases (Lon, AAA proteases) needed for refolding or degrading individual proteins, mitochondrial integrity is maintained through the regulation of protein import via the TOM/TIM complex and protein redistribution across the network via fusion and fission and through mitophagy and biogenesis, key determinants of mitochondrial turnover. A growing number of studies point to the importance of mitochondrial dynamics (fusion/fission) and mitochondrial autophagy in the heart. Mitochondrial biogenesis must keep pace with mitophagy in order to maintain a stable number of mitochondria. In this review, we will discuss the use of MitoTimer as a tool to monitor mitochondrial turnover.

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