Identification of a caspase-2 isoform that behaves as an endogenous inhibitor of the caspase cascade

Cancer Res. 2000 Dec 15;60(24):7039-47.

Abstract

Procaspase-2 is one of the aspartate-specific cysteine proteases that are activated in response to various apoptotic stimuli. Two isoforms of human procaspase-2 have been described initially. Overexpression of the long isoform (caspase-2L) promotes cell death whereas the short isoform (caspase-2S) antagonizes some apoptotic pathways. In the present study, we identified two additional CASP-2 mRNAs, designated CASP-2L-Pro and CASP-2s-Pro. The proteins encoded by these isoforms corresponded to the prodomain of procaspase-2L and -2S, in which the last alpha-helix of their caspase recruitment domains was deleted. Caspase-2L-Pro mRNA and protein were detected in a series of human tissues and cell lines. Yeast 2-hybrid assays and immunoprecipitation studies indicated that caspase-2L-Pro can interact with procaspase-2L and the adaptor protein RAIDD/CRADD, but not with FADD/MORT1 or APAF-1 adaptor proteins. The addition of recombinant caspase-2L-Pro negatively interfered with cytochrome c/dATP-mediated activation of the caspase cascade in a cell-free system. In transient expression studies of human B lymphoma Namalwa cells, overexpression of caspase-2L-Pro weakly induced apoptosis, which was prevented by a D83A/E87A double mutation. In stable selected CASP-2L-Pro-transfected Namalwa cells, overexpression of caspase-2L-Pro delayed apoptotic DNA fragmentation induced by death receptor agonists (anti-Fas antibodies, tumor necrosis factor-alpha) and DNA topoisomerase I- (camptothecin) and II- (etoposide) inhibitors, and prevented etoposide-induced activation of the caspase cascade. These inhibitory effects were not observed in stable transfected cells expressing the D83A/E87A double mutant. Altogether, these data indicated that the caspase-2L-Pro isoform functions as an endogenous apoptosis inhibitory protein that antagonizes caspase activation and cell death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Apoptosis
  • Base Sequence
  • Blotting, Southern
  • Blotting, Western
  • Caspase 2
  • Caspase Inhibitors*
  • Caspases / biosynthesis*
  • Caspases / chemistry*
  • Caspases / genetics
  • Cell Death
  • Cell Line
  • Cell-Free System
  • Cloning, Molecular
  • Cytochrome c Group / metabolism
  • DNA Fragmentation
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Etoposide / pharmacology
  • Humans
  • Kinetics
  • Lymphoma / metabolism
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Mutation
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • Precipitin Tests
  • Protein Binding
  • Protein Isoforms*
  • Protein Structure, Tertiary
  • RNA, Messenger / metabolism
  • Recombinant Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Time Factors
  • Tissue Distribution
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / metabolism
  • Two-Hybrid System Techniques

Substances

  • Antineoplastic Agents, Phytogenic
  • Caspase Inhibitors
  • Cytochrome c Group
  • Nucleic Acid Synthesis Inhibitors
  • Protein Isoforms
  • RNA, Messenger
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Etoposide
  • Caspase 2
  • Caspases