Abstract
To complete their maturation, most immature thymocytes depend on the simultaneous engagement of their antigen receptor [alpha beta T cell receptor (TCR)] and their CD4 or CD8 coreceptors with major histocompatibility complex class II or I ligands, respectively. However, a normal subset of mature alpha beta TCR+ thymocytes did not follow these rules. These thymocytes expressed NK1.1 and a restricted set of alpha beta TCRs that are intrinsically class I-reactive because their positive selection was class I-dependent but CD8-independent. These cells were CD4+ and CD4-8- but never CD8+, because the presence of CD8 caused negative selection. Thus, neither CD4 nor CD8 contributes signals that direct their maturation into the CD4+ and CD4-8- lineages.
MeSH terms
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Animals
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Antigens / analysis
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Antigens, Ly
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Antigens, Surface
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CD4 Antigens / analysis
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CD4-Positive T-Lymphocytes / cytology
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CD4-Positive T-Lymphocytes / immunology*
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CD8 Antigens / analysis
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Female
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Histocompatibility Antigens Class I / physiology*
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Lectins, C-Type
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Ligands
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Lymphocyte Activation
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Male
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Mice
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Mice, Inbred C57BL
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NK Cell Lectin-Like Receptor Subfamily B
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Phenotype
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Proteins / analysis
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Receptors, Antigen, T-Cell, alpha-beta / analysis
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Receptors, Antigen, T-Cell, alpha-beta / physiology*
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T-Lymphocyte Subsets / cytology
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T-Lymphocyte Subsets / immunology*
Substances
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Antigens
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Antigens, Ly
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Antigens, Surface
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CD4 Antigens
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CD8 Antigens
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Histocompatibility Antigens Class I
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Klrb1c protein, mouse
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Lectins, C-Type
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Ligands
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NK Cell Lectin-Like Receptor Subfamily B
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Proteins
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Receptors, Antigen, T-Cell, alpha-beta