The kinase PDK1 integrates T cell antigen receptor and CD28 coreceptor signaling to induce NF-κB and activate T cells

被引:110
|
作者
Park, Sung-Gyoo [1 ]
Schulze-Luehrman, Jan [1 ]
Hayden, Matthew S. [1 ]
Hashimoto, Naoko [2 ]
Ogawa, Wataru [2 ]
Kasuga, Masato [2 ]
Ghosh, Sankar [1 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] Kobe Univ, Grad Sch Med, Div Diabet & Digest & Kidney Dis, Dept Clin Mol Med, Kobe, Hyogo 6500017, Japan
[3] Yale Univ, Sch Med, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
3-PHOSPHOINOSITIDE-DEPENDENT PROTEIN KINASE-1; IMMUNOLOGICAL SYNAPSE; CD28-DEFICIENT MICE; PHOSPHORYLATION; CARMA1; BETA; COSTIMULATION; LYMPHOCYTES; EXPRESSION; SURVIVAL;
D O I
10.1038/ni.1687
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In addition to ligation of the T cell antigen receptor (TCR), activation of the CD28 coreceptor by the costimulatory molecule B7 is required for induction of the transcription factor NF-kappa B and robust T cell activation, although the contribution of CD28 to this process remains incompletely understood. We show here that phosphoinositide-dependent kinase 1 (PDK1) is essential for integrating the TCR and CD28 signals. After we deleted PDK1 from T cells, TCR-CD28 signals were unable to induce activation of NF-kappa B or phosphorylation of protein kinase C-theta, although T cell survival and pathways dependent on the kinases p38 and Jnk or the transcription factor NFAT were unaffected. CD28 facilitated NF-kappa B activation by regulating recruitment and phosphorylation of PDK1, which are necessary for efficient binding of PDK1 to protein kinase C-theta and the adaptor CARMA1 and thus for NF-kappa B induction.
引用
收藏
页码:158 / 166
页数:9
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