Bcl-2 Blocks Apoptosis in Cells Lacking Mitochondrial DNA

Nature. 1993 Jan 28;361(6410):365-9. doi: 10.1038/361365a0.


When the mammalian proto-oncogene bcl-2 is overexpressed it can protect various types of cells both from normal and from experimentally induced apoptosis, but the molecular mechanisms involved are unknown. Although the Bcl-2 protein is membrane-associated, its subcellular location is controversial: two studies have suggested that it is mainly associated with the nuclear envelope and endoplasmic reticulum, whereas another study has suggested that it is mainly located in the inner mitochondrial membrane. The latter study has suggested that Bcl-2 might protect cells from apoptosis by altering mitochondrial function and that mitochondria may be involved in apoptosis. Here we report that human mutant cell lines that lack mitochondrial DNA (mtDNA), and therefore do not have a functional respiratory chain, can still be induced to die by apoptosis, and that they can be protected from apoptosis by the overexpression of bcl-2, suggesting that neither apoptosis nor the protective effect of bcl-2 depends on mitochondrial respiration. We also show that the Bcl-2 protein in overexpressing cells is associated with the nuclear envelope and endoplasmic reticulum, as well as with mitochondria.

Publication types

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

MeSH terms

  • Alkaloids / pharmacology
  • Antigens, Polyomavirus Transforming / genetics
  • Apoptosis / physiology*
  • Cell Line, Transformed
  • DNA, Mitochondrial / genetics
  • DNA, Mitochondrial / metabolism*
  • Ethidium / pharmacology
  • Fluorescent Antibody Technique
  • GTP-Binding Proteins / metabolism*
  • Gene Expression
  • Humans
  • Kinetics
  • Protein Kinase C / antagonists & inhibitors
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-bcl-2
  • Proto-Oncogenes*
  • Simian virus 40 / genetics
  • Staurosporine
  • Time Factors


  • Alkaloids
  • Antigens, Polyomavirus Transforming
  • DNA, Mitochondrial
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Protein Kinase C
  • GTP-Binding Proteins
  • Ethidium
  • Staurosporine