Protein synthesis-dependent apoptotic signalling pathway in X-irradiated MOLT-4 human leukaemia cell line

Int J Radiat Biol. 2002 Feb;78(2):115-24. doi: 10.1080/09553000110076472.

Abstract

Purpose: To demonstrate whether protein synthesis is required for ionizing radiation-induced apoptosis through activation of caspases in human leukaemia cell line MOLT-4, the effects of a protein synthesis inhibitor, cycloheximide, on the apoptotic signalling pathway including the activation of caspase family and stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK), and the expression of Fas/CD95/APO-1 (Fas) were examined in X-irradiated MOLT-4 cells.

Materials and methods: MOLT-4 cells pretreated with 0.5 microg/ml cycloheximide for 1h were exposed to 7.5Gy of X-rays. The appearance of apoptosis, expression of Fas, activation of caspases-3, -8, -9, SAPK/JNK and AP-1, the release of mitochondrial cytochrome-C and the formation of death-induced signalling complex (DISC) between Fas and the Fas-associated death domain (FADD) were measured by fluorescence microscopy, Western blotting, flow cytometry, gel shift assay and immunoprecipitation, respectively.

Results: Nuclear fragmentation and chromatin condensation were observed at 6 h after X-irradiation and gradually increased up to 12 h. These phenomena were significantly attenuated by cycloheximide. Cycloheximide also inhibited the activation of caspases and AP-1, the expression of Fas, the formation of DISC and the release of cytochrome-C, but not the activation of SAPK/JNK in X-irradiated MOLT-4 cells.

Conclusion: These results indicate that apoptosis of X-ray-induced MOLT-4 cells is dependent on the activation of caspases regulated by de novo protein synthesis through SAPK/JNK activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Arabidopsis Proteins*
  • Blotting, Western
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspases / metabolism
  • Cell Nucleus / metabolism
  • Chromatin / metabolism
  • Cycloheximide / pharmacology
  • Cytochrome c Group / metabolism
  • Dose-Response Relationship, Radiation
  • Electrophoresis, Polyacrylamide Gel
  • Fatty Acid Desaturases / metabolism
  • Flow Cytometry
  • Humans
  • Immunoblotting
  • Leukemia / metabolism*
  • Leukemia / pathology*
  • MAP Kinase Kinase 4*
  • Membrane Potentials
  • Microscopy, Fluorescence
  • Mitochondria / metabolism
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Precipitin Tests
  • Protein Binding
  • Protein Biosynthesis*
  • Signal Transduction*
  • Time Factors
  • Transcription Factor AP-1 / metabolism
  • Tumor Cells, Cultured
  • X-Rays*

Substances

  • Arabidopsis Proteins
  • Chromatin
  • Cytochrome c Group
  • Transcription Factor AP-1
  • Cycloheximide
  • Fatty Acid Desaturases
  • Fad7 protein, Arabidopsis
  • MAP Kinase Kinase 4
  • MAP2K4 protein, human
  • Mitogen-Activated Protein Kinase Kinases
  • CASP3 protein, human
  • CASP8 protein, human
  • CASP9 protein, human
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspases