Abstract
The CD3gamma di-leucine-based motif plays a central role in TCR down-regulation. However, little is understood about the role of the CD3gamma di-leucine-based motif in physiological T cell responses. In this study, we show that the expansion in numbers of virus-specific CD8(+) T cells is impaired in mice with a mutated CD3gamma di-leucine-based motif. The CD3gamma mutation did not impair early TCR signaling, nor did it compromise recruitment or proliferation of virus-specific T cells, but it increased the apoptosis rate of the activated T cells by increasing down-regulation of the antiapoptotic molecule Bcl-2. This resulted in a 2-fold reduction in the clonal expansion of virus-specific CD8(+) T cells during the acute phase of vesicular stomatitis virus and lymphocytic choriomeningitis virus infections. These results identify an important role of CD3gamma-mediated TCR down-regulation in virus-specific CD8(+) T cell responses.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Motifs / genetics
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Amino Acid Motifs / immunology
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Animals
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Arenaviridae Infections / genetics
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Arenaviridae Infections / immunology*
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CD3 Complex / genetics
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CD3 Complex / immunology*
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CD8-Positive T-Lymphocytes / immunology*
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Down-Regulation / immunology*
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Lymphocytic choriomeningitis virus / immunology*
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Mice
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Mice, Transgenic
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Mutation / immunology
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Peptides / immunology
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Proto-Oncogene Proteins c-bcl-2 / genetics
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Proto-Oncogene Proteins c-bcl-2 / immunology
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Receptors, Antigen, T-Cell / genetics
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Receptors, Antigen, T-Cell / immunology*
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Rhabdoviridae Infections / genetics
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Rhabdoviridae Infections / immunology*
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Signal Transduction / genetics
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Signal Transduction / immunology
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Vesiculovirus / immunology*
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Viral Proteins / immunology
Substances
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CD3 Complex
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CD3 antigen, gamma chain
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Peptides
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Proto-Oncogene Proteins c-bcl-2
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Receptors, Antigen, T-Cell
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Viral Proteins