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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
1994-11-7
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pubmed:abstractText |
Stimulation of T cells through the T cell receptor (TcR) initiate activation pathways, and paradoxically can also result in activation-induced cell death. Many factors influence a stimulated cell's decision to manifest one or the other. Here we show that co-stimulation with LFA-1 plays a key role in the choice between the two fates, differentiating between alpha beta and gamma delta T cells. Peripheral gamma delta. T cells but not alpha beta T cells undergo apoptosis upon co-cross-linking of TcR and LFA-1 in MRL lpr/lpr mice as well as +/+ mice. Our results suggest that apoptosis of gamma delta T cells is inducible by combined stimuli independent of the Fas-mediated pathway.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0014-2980
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2441-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7925573-Animals,
pubmed-meshheading:7925573-Apoptosis,
pubmed-meshheading:7925573-DNA Damage,
pubmed-meshheading:7925573-Female,
pubmed-meshheading:7925573-Liver,
pubmed-meshheading:7925573-Lymph Nodes,
pubmed-meshheading:7925573-Lymphocyte Activation,
pubmed-meshheading:7925573-Lymphocyte Function-Associated Antigen-1,
pubmed-meshheading:7925573-Mice,
pubmed-meshheading:7925573-Mice, Mutant Strains,
pubmed-meshheading:7925573-Receptor Aggregation,
pubmed-meshheading:7925573-Receptors, Antigen, T-Cell, gamma-delta,
pubmed-meshheading:7925573-T-Lymphocyte Subsets
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pubmed:year |
1994
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pubmed:articleTitle |
Co-stimulation with LFA-1 triggers apoptosis in gamma delta T cells on T cell receptor engagement.
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pubmed:affiliation |
Department of Internal Medicine, Nagoya University Branch Hospital, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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