A brief overview of BNIP3L/NIX receptor-mediated mitophagy

FEBS Open Bio. 2021 Dec;11(12):3230-3236. doi: 10.1002/2211-5463.13307. Epub 2021 Oct 11.

Abstract

Mitophagy is a form of autophagy specialized to selectively remove mitochondria. Although the PINK1/Parkin pathway is the best described mitophagy of damaged mitochondria, receptor/mediated mitophagy seems to have a pivotal role in cellular development and specialization. The most studied mitophagy receptor BCL2/adenovirus E1B 19-kDa-interacting protein 3-like (BNIP3L/NIX) is shown to be important for the programmed removal of healthy mitochondria during terminal differentiation of erythrocytes, but its role has been proven in various cell types. Despite recent advances in our understanding of its regulation by phosphorylation and dimerization, there remain numerous questions on how BNIP3L/NIX tightly balances between cellular life and death decisions. This brief review intends to summarize ongoing dilemmas related to BNIP3L/NIX.

Keywords: BNIP3L/NIX; mitochondria; mitophagy; reticulocytes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Apoptosis Regulatory Proteins / metabolism
  • Autophagy / physiology
  • Cell Differentiation
  • Humans
  • Membrane Proteins / metabolism*
  • Membrane Proteins / physiology
  • Mitochondria / metabolism
  • Mitochondrial Proteins / metabolism
  • Mitophagy / physiology*
  • Phosphorylation
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins / physiology
  • Tumor Suppressor Proteins / metabolism*
  • Tumor Suppressor Proteins / physiology
  • Ubiquitin-Protein Ligases

Substances

  • Apoptosis Regulatory Proteins
  • BNIP3L protein, human
  • Membrane Proteins
  • Mitochondrial Proteins
  • Proto-Oncogene Proteins
  • Tumor Suppressor Proteins
  • Ubiquitin-Protein Ligases
  • parkin protein