The CD99 signal enhances Fas-mediated apoptosis in the human leukemic cell line, Jurkat

FEBS Lett. 2003 Nov 20;554(3):478-84. doi: 10.1016/s0014-5793(03)01224-9.

Abstract

The CD99 antigen has been implicated in various cellular processes, including apoptosis in T cells. Previously, we reported two monoclonal antibodies that recognize different epitopes of the CD99 molecule, named DN16 and YG32. In this study, we investigated the role of each CD99 epitope in T cell apoptosis. Unlike the DN16 epitope, CD99 ligation via the YG32 epitope failed to induce T cell death. Surprisingly, however, the YG32 signal enhanced Fas-mediated apoptosis in Jurkat T cells. Augmentation of Fas-mediated apoptosis by YG32 ligation was inhibited by treatment with either of the caspase inhibitors z-VAD-fmk or z-IETD-fmk, and YG32 ligation appeared to induce Fas oligomerization. These results suggest that each CD99 epitope plays a distinct role in T cell biology, especially in T cell apoptosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 12E7 Antigen
  • Amino Acid Chloromethyl Ketones / pharmacology
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Monoclonal / immunology
  • Antigens, CD / chemistry
  • Antigens, CD / immunology
  • Antigens, CD / metabolism*
  • Apoptosis / physiology*
  • Caspase Inhibitors
  • Caspases / metabolism
  • Cell Adhesion Molecules / chemistry
  • Cell Adhesion Molecules / immunology
  • Cell Adhesion Molecules / metabolism*
  • Cell Aggregation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Epitopes, T-Lymphocyte / immunology
  • Epitopes, T-Lymphocyte / metabolism
  • Epitopes, T-Lymphocyte / pharmacology
  • Humans
  • Immunohistochemistry / methods
  • Jurkat Cells
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Microscopy, Confocal
  • Mitochondria / drug effects
  • Mitochondria / physiology
  • Signal Transduction / physiology
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / metabolism
  • fas Receptor / chemistry
  • fas Receptor / metabolism*
  • fas Receptor / ultrastructure

Substances

  • 12E7 Antigen
  • Amino Acid Chloromethyl Ketones
  • Antibodies, Monoclonal
  • Antigens, CD
  • CD99 protein, human
  • Caspase Inhibitors
  • Cell Adhesion Molecules
  • Enzyme Inhibitors
  • Epitopes, T-Lymphocyte
  • benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone
  • fas Receptor
  • Caspases