December 1998
Volume 39, Issue 13
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Articles  |   December 1998
Involvement of interleukin-1beta-converting enzyme in apoptosis of irradiated retinoblastomas.
Author Affiliations
  • Y Kondo
    Department of Neurosciences, Brain Tumor/Neuro-Oncology Center, The Cleveland Clinic Foundation, Ohio 44195, USA.
  • J Liu
    Department of Neurosciences, Brain Tumor/Neuro-Oncology Center, The Cleveland Clinic Foundation, Ohio 44195, USA.
  • T Haqqi
    Department of Neurosciences, Brain Tumor/Neuro-Oncology Center, The Cleveland Clinic Foundation, Ohio 44195, USA.
  • B P Barna
    Department of Neurosciences, Brain Tumor/Neuro-Oncology Center, The Cleveland Clinic Foundation, Ohio 44195, USA.
  • S Kondo
    Department of Neurosciences, Brain Tumor/Neuro-Oncology Center, The Cleveland Clinic Foundation, Ohio 44195, USA.
Investigative Ophthalmology & Visual Science December 1998, Vol.39, 2769-2774. doi:
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    • Get Citation

      Y Kondo, J Liu, T Haqqi, B P Barna, S Kondo; Involvement of interleukin-1beta-converting enzyme in apoptosis of irradiated retinoblastomas.. Invest. Ophthalmol. Vis. Sci. 1998;39(13):2769-2774.

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Abstract

PURPOSE: To investigate whether interleukin-1beta-converting enzyme (ICE), a mammalian homologue of the Caenorhabditis elegans cell death gene ced-3, is involved in gamma-irradiation-induced apoptosis (programmed cell death) of human retinoblastoma cells. METHODS: The induction of apoptotic cell death in human retinoblastoma cell lines WERI-Rb-1 and Y79 by gamma-irradiation was determined with a modified 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl tetrazolium bromide colorimetric assay and the DNA-binding fluorochrome bis (benzimide) trihydro-chloride (Hoechst 33258) staining. The change of ICE protein level in tumor cells during apoptosis was determined by immunoblotting assay. Whether the specific tetrapeptide ICE inhibitor Ac-YVAD-CMK affected gamma-irradiation-induced apoptosis in tumor cells was also examined. The effect of ICE overexpression on tumor cells was evaluated by a transient transfection assay using ICE expression vector. RESULTS: Gamma-irradiation inhibited the cell viability of WERI-Rb-1 and Y79 cells in a dose-dependent manner and induced apoptosis. The protein level of ICE was remarkably enhanced after the treatment. The apoptotic cell death induced by gamma-irradiation was suppressed by the tetrapeptide ICE inhibitor Ac-YVAD-CMK. Moreover, overexpression of ICE induced apoptosis in tumor cells. CONCLUSIONS: These findings suggest that ICE may play an important role in gamma-irradiation-induced apoptosis in retinoblastoma cells. Transfer of the ICE gene induces apoptosis in these cells without gamma-irradiation.

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