Ceramide induces mitochondrial activation and apoptosis via a Bax-dependent pathway in human carcinoma cells

Oncogene. 2002 Jun 6;21(25):4009-19. doi: 10.1038/sj.onc.1205497.

Abstract

The intracellular pathways leading to mitochondrial activation and subsequent cell death in the ceramide-mediated stress response have been intensively studied in recent years. Experimental evidence has been provided that ceramide-induced apoptosis is inhibited by overexpression of antiapoptotic proteins of the Bcl-2 family. However, the direct effect of proapoptotic gene products, e.g. Bax, on ceramide-induced death signalling has not yet been studied in detail. In the present work, we show by measurement of mitochondrial permeability transition, cytochrome c release, activation of caspase-3 and DNA fragmentation that ceramide-induced apoptosis is marginal in Bax-negative DU 145 cells. Reconstitution of Bax by generation of DU 145 cells stably expressing this proapoptotic factor, clearly enhanced ceramide-induced apoptosis at all levels of the mitochondrial signalling cascade. Using the broad-range caspase inhibitor zVAD-fmk and zDEVD-fmk, an inhibitor of caspase-3-like activities, we demonstrate that the ceramide-induced mitochondrial activation in Bax-transfected DU 145 cells is caspase-independent. On the other hand, apoptotic events located downstream of the mitochondria, e.g. DNA fragmentation, were shown to be caspase-dependent. This influence of Bax on ceramide-induced apoptosis was confirmed in another cellular system: whereas Bax-positive HCT116 wild type cells were very sensitive towards induction of cell death by C(2)-ceramide, sensitivity of Bax knock-out HCT116 cells was significantly reduced. Thus, we conclude that Bax is a key activator of ceramide-mediated death pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Chloromethyl Ketones / pharmacology
  • Antibiotics, Antineoplastic / pharmacology
  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspase 3
  • Caspase Inhibitors
  • Caspases / metabolism
  • Cell Fractionation
  • Ceramides / pharmacology*
  • Cysteine Proteinase Inhibitors / pharmacology
  • Cytochrome c Group / metabolism
  • Epirubicin / pharmacology
  • Flow Cytometry
  • Humans
  • Male
  • Mitochondria / metabolism*
  • Oligopeptides / pharmacology
  • Prostatic Neoplasms / metabolism*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-bcl-2*
  • Retroviridae / genetics
  • Signal Transduction
  • Transfection
  • Tumor Cells, Cultured
  • bcl-2-Associated X Protein

Substances

  • Amino Acid Chloromethyl Ketones
  • Antibiotics, Antineoplastic
  • BAX protein, human
  • Caspase Inhibitors
  • Ceramides
  • Cysteine Proteinase Inhibitors
  • Cytochrome c Group
  • Oligopeptides
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • benzoylcarbonyl-aspartyl-glutamyl-valyl-aspartyl-fluoromethyl ketone
  • benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone
  • Epirubicin
  • CASP3 protein, human
  • Caspase 3
  • Caspases