Autophagy as a protective response to Bnip3-mediated apoptotic signaling in the heart

Autophagy. 2006 Oct-Dec;2(4):307-9. doi: 10.4161/auto.2947. Epub 2006 Oct 25.

Abstract

Bnip3 is a member of the 'BH3-only' Bcl-2 subfamily which has been implicated in apoptotic,(1) necrotic(2) and autophagic cell death.(3,4) We recently reported that Bnip3 is a key mediator of mitochondrial dysfunction and cell death in the ex vivo heart following ischemia/reperfusion (I/R).(5) Moreover, we found that Bnip3 was involved in upregulation of autophagy in I/R and that Bnip3-mediated mitochondrial dysfunction correlated with upregulation of autophagy. Using a model of simulated I/R and overexpression of Bnip3 in HL-1 cardiac myocytes, we determined that Bnip3-mediated upregulation of autophagic activity constituted a protective response against Bnip3 death signaling. Here we present additional evidence that enhanced autophagic activity functions as a cytoprotective pathway to oppose ischemia/reperfusion-related apoptosis.

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Apoptosis Regulatory Proteins
  • Autophagy / physiology*
  • Beclin-1
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • Myocardium / metabolism*
  • Proteins / genetics
  • Proteins / metabolism
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Signal Transduction / physiology*

Substances

  • Apoptosis Regulatory Proteins
  • BNip3 protein, mouse
  • Beclin-1
  • Becn1 protein, mouse
  • Membrane Proteins
  • Mitochondrial Proteins
  • Proteins