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Immunity ; 21(2): 167-77, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15308098

ABSTRACT

Antigen-specific immunotolerance limits the expansion of self-reactive T cells involved in autoimmune diseases. Here, we show that the E3 ubiquitin ligase Cbl-b is upregulated in T cells after tolerizing signals. Loss of Cbl-b in mice results in impaired induction of T cell tolerance both in vitro and in vivo. Importantly, rechallenge of Cbl-b mutant mice with the tolerizing antigen results in massive lethality. Moreover, ablation of Cbl-b resulted in exacerbated autoimmunity. Mechanistically, loss of Cbl-b rescues reduced calcium mobilization of anergic T cells, which was attributed to Cbl-b-mediated regulation of PLCgamma-1 phosphorylation. Our results show a critical role for Cbl-b in the regulation of peripheral tolerance and anergy of T cells.


Subject(s)
Adaptor Proteins, Signal Transducing , Clonal Anergy/immunology , T-Lymphocytes/metabolism , Ubiquitin-Protein Ligases/metabolism , Adoptive Transfer , Animals , Antigens/immunology , Clonal Anergy/physiology , Enterotoxins/immunology , In Vitro Techniques , Mice , Phospholipase C gamma , Proto-Oncogene Proteins c-cbl , T-Lymphocytes/immunology , Type C Phospholipases/metabolism , Ubiquitin-Protein Ligases/immunology
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