The Notch regulator Numb links the Notch and TCR signaling pathways

被引:48
|
作者
Anderson, AC
Kitchens, EA
Chan, SW
Hill, CS
Jan, YN
Zhong, WM
Robey, EA
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Biochem, San Francisco, CA 94143 USA
[5] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
来源
JOURNAL OF IMMUNOLOGY | 2005年 / 174卷 / 02期
关键词
D O I
10.4049/jimmunol.174.2.890
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Both the Notch and TCR signaling pathways play an important role in T cell development, but the links between these signaling pathways are largely unexplored. The adapter protein Numb is a well-characterized inhibitor of Notch and also contains a phosphotyrosine binding domain, suggesting that Numb could provide a link between these pathways. We explored this possibility by investigating the physical interactions among Notch, Numb, and the TCR signaling apparatus and by examining the consequences of a Numb mutation on T cell development. We found that Notch and Numb cocluster with the TCR at the APC contact during Ag-driven T cell-APC interactions in both immature and mature T cells. Furthermore, Numb coimmunoprecipitates with components of the TCR signaling apparatus. Despite this association, T cell development and T cell activation occur normally in the absence of Numb, perhaps due to the expression of the related protein, Numblike. Together our data suggest that Notch and TCR signals may be integrated at the cell membrane, and that Numb may be an important adapter in this process.
引用
收藏
页码:890 / 897
页数:8
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