PGAM5: A crucial role in mitochondrial dynamics and programmed cell death

Eur J Cell Biol. 2021 Jan;100(1):151144. doi: 10.1016/j.ejcb.2020.151144. Epub 2020 Dec 7.

Abstract

In response to mitochondrial damage, mitochondria activate mitochondrial dynamics to maintain normal functions, and an imbalance in mitochondrial dynamics triggers multiple programmed cell death processes. Recent studies have shown that phosphoglycerate mutase 5 (PGAM5) is associated with mitochondrial damage. PGAM5 activates mitochondrial biogenesis and mitophagy to promote a cellular compensatory response when mitochondria are mildly damaged, whereas severe damage to mitochondria leads to PGAM5 inducing excessive mitochondria fission, disruption to mitochondrial movement, and amplification of apoptosis, necroptosis and mitophagic death signals, which eventually evoke cell death. PGAM5 functions mainly through protein-protein interactions and specific Ser/Thr/His protein phosphatase activity. PGAM5 is also regulated by mitochondrial proteases. Detection of PGAM5 and its interacting protein partners should enable a more accurate evaluation of mitochondrial damage and a more precise method for the diagnosis and treatment of diseases.

Keywords: Apoptosis; Mitochondrial dynamics; Mitochondrial proteases; Necroptosis; PGAM5.

Publication types

  • Review

MeSH terms

  • Apoptosis / genetics*
  • Humans
  • Mitochondrial Dynamics / genetics*
  • Mitochondrial Proteins / metabolism*
  • Mitophagy / genetics*
  • Necroptosis / genetics*
  • Phosphoprotein Phosphatases / metabolism*

Substances

  • Mitochondrial Proteins
  • PGAM5 protein, human
  • Phosphoprotein Phosphatases