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The CD99 signal enhances Fas-mediated apoptosis in the human leukemic cell line, Jurkat.
- Source :
-
FEBS letters [FEBS Lett] 2003 Nov 20; Vol. 554 (3), pp. 478-84. - Publication Year :
- 2003
-
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.
- Subjects :
- 12E7 Antigen
Amino Acid Chloromethyl Ketones pharmacology
Antibodies, Monoclonal chemistry
Antibodies, Monoclonal immunology
Antigens, CD chemistry
Antigens, CD immunology
Caspase Inhibitors
Caspases metabolism
Cell Adhesion Molecules chemistry
Cell Adhesion Molecules immunology
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 metabolism
fas Receptor chemistry
fas Receptor ultrastructure
Antigens, CD metabolism
Apoptosis physiology
Cell Adhesion Molecules metabolism
T-Lymphocytes cytology
fas Receptor metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 554
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 14623115
- Full Text :
- https://doi.org/10.1016/s0014-5793(03)01224-9