A novel functional interaction between Vav and PKCθ is required for TCR-induced T cell activation

被引:197
作者
Villalba, M
Coudronniere, N
Deckert, M
Teixeiro, E
Mas, P
Altman, A [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Cell Biol, San Diego, CA 92121 USA
[2] Univ Complutense Madrid, Fdn Jimenez Diaz, Dept Immunol, E-28040 Madrid, Spain
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1016/S1074-7613(00)80168-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vav and PKC theta play an early and important role in the TCR/CD28-induced stimulation of MAP kinases and activation of the IL-2 gene. Vav is also essential for actin cytoskeleton reorganization and TCR capping. Here, we report that PKC theta function was selectively required in a Vav signaling pathway that mediates the TCR/CD28-induced activation of JNK and the IL-2 gene and the upregulation of CD69 expression. Vav also promoted PKC theta translocation from the cytosol to the membrane and cytoskeleton and induced its enzymatic activation in a CD3/CD28-initiated pathway that was dependent on Rac and on actin cytoskeleton reorganization. These findings reveal that the Vav/Rac pathway promotes the recruitment of PKC theta to the T cell synapse and its activation, essential processes for T cell activation and IL-2 production.
引用
收藏
页码:151 / 160
页数:10
相关论文
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