Regulation of the Fas apoptotic cell death pathway by Abl

J Biol Chem. 1995 Sep 22;270(38):22625-31. doi: 10.1074/jbc.270.38.22625.

Abstract

Relatively little is known about oncogene involvement in the regulation of Fas-mediated apoptosis. Inhibition of Fas-induced cell death by the bcl-2 oncogene has been demonstrated to be only partial. In light of a growing body of evidence for the Abl kinase as a negative regulator of cell death, we sought to determine whether Abl expression could protect against Fas-mediated cell death. To address this question, we utilized two separate strategies. In the first, we expressed human Fas in K562, a chronic myelogenous leukemia cell line, which constitutively expresses bcr-abl and examined the effects of Fas ligation in these cells. Fas-positive K562 transformants (K562.Fas) were found to be protected against Fas-mediated cell death. However, down-regulation of Bcr-Abl protein levels in K562.Fas cells using antisense oligonucleotides targeted to bcr-abl mRNA rendered these cells highly susceptible to Fas-induced death. In the second approach we utilized a Fas-positive HL-60 cell line, which we transfected with a temperature-sensitive mutant of v-Abl. HL-60.v-Ablts transfectants were found to be protected from Fas-induced apoptosis at the permissive but not the restrictive temperature for the Abl kinase. Taken together, these observations identify the Abl kinase as a negative regulator of Fas-mediated cell death. Since Abl was also found to block apoptosis mediated by ceramide, a recently proposed downstream effector of the apoptotic pathway initiated by Fas, we propose that Abl exerts its protective effects downstream of the early Fas-initiated signaling events.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Surface / physiology*
  • Apoptosis* / drug effects
  • Base Sequence
  • Ceramides / pharmacology
  • DNA Damage
  • Fusion Proteins, bcr-abl / metabolism*
  • Humans
  • In Vitro Techniques
  • Molecular Sequence Data
  • Oligonucleotides, Antisense / chemistry
  • Oncogene Proteins v-abl / metabolism
  • Proto-Oncogene Proteins c-abl / physiology*
  • Transfection
  • Tumor Cells, Cultured
  • fas Receptor

Substances

  • Antigens, Surface
  • Ceramides
  • Oligonucleotides, Antisense
  • Oncogene Proteins v-abl
  • fas Receptor
  • Fusion Proteins, bcr-abl
  • Proto-Oncogene Proteins c-abl