Physiological and Pharmacological Control of BAK, BAX, and Beyond

Trends Cell Biol. 2016 Dec;26(12):906-917. doi: 10.1016/j.tcb.2016.07.002. Epub 2016 Aug 4.

Abstract

Cellular commitment to the mitochondrial pathway of apoptosis is accomplished when proapoptotic B cell chronic lymphocytic leukemia/lymphoma (BCL)-2 proteins compromise mitochondrial integrity through the process of mitochondrial outer membrane permeabilization (MOMP). For nearly three decades, intensive efforts focused on the identification and interactions of two key proapoptotic BCL-2 proteins: BCL-2 antagonist killer (BAK) and BCL-2-associated X (BAX). Indeed, we now have critical insights into which BCL-2 proteins interact with BAK/BAX to either preserve survival or initiate MOMP. In contrast, while mitochondria are targeted by BAK/BAX, a molecular understanding of how these organelles govern BAK/BAX function remains less clear. Here, we integrate recent mechanistic insights of proapoptotic BCL-2 protein function in the context of mitochondrial environment, and discuss current and potential pharmacological opportunities to control MOMP in disease.

Keywords: BCL-2 family; BH3 mimetics; apoptosis; mitochondria; mitochondrial outer membrane permeabilization.

Publication types

  • Review
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis
  • Humans
  • Membrane Potential, Mitochondrial
  • Mitochondria / metabolism
  • Models, Biological
  • bcl-2 Homologous Antagonist-Killer Protein / chemistry
  • bcl-2 Homologous Antagonist-Killer Protein / metabolism*
  • bcl-2-Associated X Protein / chemistry
  • bcl-2-Associated X Protein / metabolism*

Substances

  • bcl-2 Homologous Antagonist-Killer Protein
  • bcl-2-Associated X Protein