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Mitochondrial biogenesis and clearance: a balancing act

FEBS J. 2017 Jan;284(2):183-195. doi: 10.1111/febs.13820. Epub 2016 Aug 11.

Abstract

Mitochondria are semi-autonomous organelles of prokaryotic origin that are postulated to have been acquired by eukaryotic cells through an early endosymbiotic event. Except for their main role in energy production, they are also implicated in fundamental cellular processes, including ion homeostasis, lipid metabolism, and initiation of apoptotic cell death. Perturbed mitochondrial function has been correlated with severe human pathologies such as type-2 diabetes, cardiovascular, and neurodegenerative diseases. Thus, proper mitochondrial physiology is a prerequisite for health and survival. Cells have developed sophisticated and elaborate mechanisms to adapt to stress conditions and alterations in metabolic demands, by regulating mitochondrial number and function. Hence, the generation of new and the removal of damaged or unwanted mitochondria are highly regulated processes that need to be accurately coordinated for the maintenance of mitochondrial and cellular homeostasis. Here, we survey recent research findings that advance our understanding and highlight the importance of the underlying molecular mechanisms.

Keywords: Parkin; autophagy; mitochondrial biogenesis; mitophagy; nuclear respiratory factors.

Publication types

  • Review

MeSH terms

  • Apoptosis
  • Argonaute Proteins / genetics
  • Argonaute Proteins / metabolism
  • Cardiovascular Diseases / genetics*
  • Cardiovascular Diseases / metabolism
  • Cardiovascular Diseases / pathology
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / pathology
  • Gene Expression Regulation
  • Homeostasis
  • Humans
  • Iron / metabolism
  • Lipid Metabolism
  • Mitochondria / genetics*
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mitophagy*
  • NF-E2-Related Factor 1 / genetics
  • NF-E2-Related Factor 1 / metabolism
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / pathology
  • Organelle Biogenesis*

Substances

  • AGO2 protein, human
  • Argonaute Proteins
  • Mitochondrial Proteins
  • NF-E2-Related Factor 1
  • NFE2L1 protein, human
  • Iron