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J Biol Chem, Vol. 273, Issue 44, 28852-28859, October 30, 1998
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From the The Reaper (Rpr) gene encodes a 65-amino acid
protein that induces apoptosis in Drosophila by an unknown
mechanism. A previous study reported that Rpr expression induced
generation of the lipid second messenger ceramide and through use of
the peptide caspase inhibitor
N-benzyloxycarbonyl-VAD-fluoromethylketone(zVAD.fmk) ordered ceramide generation downstream of caspases in SL2 cells (Pronk,
G. J., Ramer, K., Amiri, P., and Williams, L. T. (1996) Science 271, 808-810). The present study re-evaluates
these events in SL2 cells transfected with cDNA for Rpr, with or
without the baculovirus caspase inhibitor p35, under the control of the
metallothionein promoter. Following copper addition, Rpr protein was
detected at 1.5 h and maximal at 2.5 h. Ceramide generation
and caspase activation occurred nearly simultaneously, each detectable
at 2-2.5 h and maximal at 6 h. Ceramide levels increased from a
base line of 5 pmol/nmol lipid phosphorus to a maximum of 10 pmol/nmol lipid phosphorus. Identical increases in ceramide were detected using
the enzymatic 1,2-diacylglycerol kinase assay or the non-enzymatic o-phthalaldehyde derivatization high pressure liquid
chromatography assay. In contrast, diacylglycerol levels were not
increased by Rpr expression. Apoptosis, first detected at 4 h, was
maximal at 16 h. Co-expression of p35 did not affect Rpr-induced
ceramide generation, whereas caspase activation and apoptosis were
abolished. In contrast, zVAD.fmk inhibited ceramide generation and
apoptosis. These data show that Rpr-induced ceramide generation is
upstream or independent of p35-inhibitable caspases and demonstrate
differences in the actions of peptide and p35 caspase inhibitors.
Laboratory of Signal Transduction, Memorial
Sloan-Kettering Cancer Center, New York, New York 10021 and the
¶ Department of Cell Biology and Neuroscience, University of Texas
Southwestern Medical Center, Dallas, Texas 75235
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