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Localization of Fas ligand in cytoplasmic granules of CD8+ cytotoxic T lymphocytes and natural killer cells: participation of Fas ligand in granule exocytosis model of cytotoxicity
- Source :
- Biochemical and biophysical research communications. 296(2)
- Publication Year :
- 2002
-
Abstract
- Fas ligand (FasL) has been implicated in cytotoxic T lymphocyte (CTL)- and natural killer (NK) cell-mediated cytotoxicity. In the present study, we investigated the localization of FasL in murine CTL and NK cells. Immunocytochemical staining showed that FasL was stored in cytoplasmic granules of CD8+ CTL clones and in vivo activated CTL and NK cells, where perforin and granzyme A also resided. Immunoelectron microscopy revealed that FasL was localized on outer membrane of the cytoplasmic granules, while perforin was localized in internal vesicles. Western blot analysis showed that the membrane-type FasL of 40 kDa was stored in CD8+ CTL clones but not in CD4+ CTL clones. By utilizing a granule exocytosis inhibitor (TN16), we demonstrated that FasL translocated onto cell surface upon degranulation of anti-CD3-stimulated CD8+ CTL clones. Moreover, TN16 markedly inhibited the FasL-mediated cytotoxicity by CD8+ T cell clones and NK cells. These results suggested a substantial contribution of FasL to granule exocytosis-mediated target cell lysis by CD8+ CTL and NK cells.
- Subjects :
- Cytotoxicity, Immunologic
Pore Forming Cytotoxic Proteins
Fas Ligand Protein
T cell
Biophysics
chemical and pharmacologic phenomena
Cytoplasmic Granules
Biochemistry
Exocytosis
Interleukin 21
Mice
medicine
Cytotoxic T cell
Animals
Humans
Molecular Biology
Cells, Cultured
Mice, Inbred BALB C
Mice, Inbred C3H
Lymphokine-activated killer cell
Membrane Glycoproteins
biology
Chemistry
Perforin
Degranulation
hemic and immune systems
Cell Biology
Natural killer T cell
Flow Cytometry
Molecular biology
Pyrrolidinones
Cell biology
Killer Cells, Natural
Mice, Inbred C57BL
CTL
medicine.anatomical_structure
Antigens, Surface
biology.protein
T-Lymphocytes, Cytotoxic
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 296
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Biochemical and biophysical research communications
- Accession number :
- edsair.doi.dedup.....f798a44afc077d35f91431a7f5aea70a