Metabolic control of mitophagy

Author:

Zimmermann Andreas12ORCID,Madeo Frank123,Diwan Abhinav4,Sadoshima Junichi5,Sedej Simon367,Kroemer Guido8910,Abdellatif Mahmoud3689ORCID

Affiliation:

1. Institute of Molecular Biosciences University of Graz Graz Austria

2. Field of Excellence BioHealth–University of Graz Graz Austria

3. BioTechMed Graz Graz Austria

4. Division of Cardiology and Center for Cardiovascular Research Washington University School of Medicine, and John Cochran Veterans Affairs Medical Center St. Louis Missouri USA

5. Department of Cell Biology and Molecular Medicine Rutgers New Jersey Medical School Newark New Jersey USA

6. Department of Cardiology Medical University of Graz Graz Austria

7. Faculty of Medicine, Institute of Physiology University of Maribor Maribor Slovenia

8. Metabolomics and Cell Biology Platforms Institut Gustave Roussy Villejuif France

9. Centre de Recherche des Cordeliers, Equipe labellisée par la Ligue contre le cancer, Université de Paris, Sorbonne Université, INSERM U1138 Institut Universitaire de France Paris France

10. Department of Biology, Hôpital Européen Georges Pompidou Institut du Cancer Paris CARPEM Paris France

Abstract

AbstractMitochondrial dysfunction is a major hallmark of ageing and related chronic disorders. Controlled removal of damaged mitochondria by the autophagic machinery, a process known as mitophagy, is vital for mitochondrial homeostasis and cell survival. The central role of mitochondria in cellular metabolism places mitochondrial removal at the interface of key metabolic pathways affecting the biosynthesis or catabolism of acetyl‐coenzyme A, nicotinamide adenine dinucleotide, polyamines, as well as fatty acids and amino acids. Molecular switches that integrate the metabolic status of the cell, like AMP‐dependent protein kinase, protein kinase A, mechanistic target of rapamycin and sirtuins, have also emerged as important regulators of mitophagy. In this review, we discuss how metabolic regulation intersects with mitophagy. We place special emphasis on the metabolic regulatory circuits that may be therapeutically targeted to delay ageing and mitochondria‐associated chronic diseases. Moreover, we identify outstanding knowledge gaps, such as the ill‐defined distinction between basal and damage‐induced mitophagy, which must be resolved to boost progress in this area.

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

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