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β-Catenin Regulates Positive Selection of Thymocytes but Not Lineage Commitment
Author(s) -
Qing Yu,
Jyoti Misra Sen
Publication year - 2007
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.178.8.5028
Subject(s) - thymocyte , cd8 , biology , lineage (genetic) , cytolysis , microbiology and biotechnology , negative selection , mhc class i , t cell receptor , t cell , major histocompatibility complex , mhc class ii , immunology , cytotoxic t cell , genetics , antigen , gene , in vitro , immune system , genome
Positive selection and lineage commitment to the cytolytic or helper lineage of T cells result in coordinated expression of MHC class I-restricted TCR and CD8 coreceptor or MHC class II-restricted TCR and CD4 molecule. Positive selection signals also regulate the survival and generation of requisite numbers of cytolytic or Th cells. beta-Catenin is the major transcriptional cofactor of T cell factor and plays a role in thymocyte development. In this study, using mice expressing stabilized beta-catenin and mice with T cell-specific deletion of beta-catenin, we show that beta-catenin regulates positive selection, but not lineage commitment of thymocytes. Furthermore, beta-catenin expression accelerates the timing of mature CD8 thymocyte generation such that CD4 and CD8 single-positive thymocytes mature with the same kinetics during development.

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