Abstract
Misselected CD8 cells that express T cell receptors (TCRs) that do not recognize class I major histocompatibility complex (MHC) protein can emerge from thymic selection. A postthymic quality control mechanism that purges these cells from the repertoire is defined here. The failure of mature CD8 cells to simultaneously engage their TCR and CD8 coreceptor triggers an activation process that begins with inhibition of CD8 gene expression through remethylation and concludes with up-regulation of surface Fas and Fas ligand and cellular apoptosis. Thus, inhibition of a death signal through continued TCR-CD8 coengagement of MHC molecules is a key checkpoint for the continued survival of correctly selected T cells. Molecular defects that prevent delivery of the death signal to mistakenly selected T cells underlie the expansion of double-negative T cells, which is the cellular signature of a subset of systemic autoimmune diseases.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adoptive Transfer
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Animals
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Apoptosis*
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CD8 Antigens / genetics*
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CD8-Positive T-Lymphocytes / cytology*
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CD8-Positive T-Lymphocytes / immunology*
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DNA Methylation*
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Fas Ligand Protein
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Gene Expression Regulation
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Granzymes
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Histocompatibility Antigens Class I / immunology
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Kruppel-Like Transcription Factors
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Lymphocyte Count
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Membrane Glycoproteins / genetics
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Mice
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Mice, Inbred C57BL
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Receptors, Antigen, T-Cell / genetics
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Receptors, Antigen, T-Cell / immunology
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Serine Endopeptidases / genetics
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Thymus Gland / immunology
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Trans-Activators / genetics
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Up-Regulation
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fas Receptor / genetics
Substances
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CD8 Antigens
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CD8 receptor
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Fas Ligand Protein
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Fasl protein, mouse
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Histocompatibility Antigens Class I
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Klf2 protein, mouse
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Kruppel-Like Transcription Factors
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Membrane Glycoproteins
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Receptors, Antigen, T-Cell
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Trans-Activators
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fas Receptor
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Granzymes
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Gzmb protein, mouse
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Serine Endopeptidases