期刊
IMMUNITY
卷 15, 期 5, 页码 847-859出版社
CELL PRESS
DOI: 10.1016/S1074-7613(01)00233-3
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资金
- NIAID NIH HHS [R01 AI054839, AI42964] Funding Source: Medline
One mechanism cytotoxic T lymphocytes use to kill targets is exocytosis of cytotoxic agents from lytic granules, a process that requires Ca2+ influx. We investigated the role of Ca2+ influx in granule exocytosis using TALL-104 human leukemic cytotoxic T cells triggered via a bispecific antibody containing an anti-CD3 F(ab') to kill Raji B lymphoma cells. Using a novel fluorescence method, we detected target-directed release of similar to 15% of lytic granules during killing. Consistent with previous work, we observed sustained CTL Ca2+ gradients during killing, but gradients reflect the behavior of Fura-2 in granules. Rapid imaging experiments suggest that Ca2+ channels are not polarized during killing, indicating that Ca2+ influx does not direct granule reorientation. Furthermore, we find that Ca2+ acts via a high-affinity interaction to promote granule exocytosis.
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