Essential role of the E3 ubiquitin ligase Cbl-b in T cell anergy induction

被引:281
作者
Jeon, MS
Atfield, A
Venuprasad, K
Krawczyk, C
Sarao, R
Elly, C
Yang, C
Arya, S
Bachmaier, K
Su, L
Bouchard, D
Jones, R
Gronski, M
Ohashi, P
Wada, T
Bloom, D
Fathman, CG
Liu, YC
Penninger, JM [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Cell Biol, San Diego, CA 92121 USA
[2] Austrian Acad Sci, Inst Mol Biotechnol, A-1030 Vienna, Austria
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[4] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A1, Canada
[5] Univ Toronto, Dept Med Biophys, Toronto, ON M5S 1A1, Canada
[6] Stanford Univ, Sch Med, Div Immunol & Rheumatol, Dept Med, Stanford, CA 94305 USA
关键词
D O I
10.1016/j.immuni.2004.07.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antigen-specific immunotolerance limits the expansion of self-reactive T cells involved in autoimmune diseases. Here, we show that the E3 ubiquitin ligase CbI-b is upregulated in T cells after tolerizing signals. Loss of CbI-b in mice results in impaired induction of T cell tolerance both in vitro and in vivo. Importantly, rechallenge of CbI-b mutant mice with the tolerizing antigen results in massive lethality. Moreover, ablation of CbI-b resulted in exacerbated autoimmunity. Mechanistically, loss of CbI-b rescues reduced calcium mobilization of anergic T cells, which was attributed to CbI-b-mediated regulation of PLCgamma-1 phosphorylation. Our results show a critical role for CbI-b in the regulation of peripheral tolerance and anergy of T cells.
引用
收藏
页码:167 / 177
页数:11
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