TCR-induced, PKC-θ-mediated NF-κB activation is regulated by a caspase-8-caspase-9-caspase-3 cascade

被引:21
作者
Zhao, Yixia [1 ,3 ]
Lei, Minxiang [2 ]
Wang, Zhaoyuan [2 ]
Qiao, Guilin [2 ]
Yang, Tianlun [1 ]
Zhang, Jian [2 ,3 ]
机构
[1] Cent S Univ, Xiangya Hosp, Dept Cardiol, Changsha 41000, Hunan, Peoples R China
[2] Univ Chicago, Dept Med, Nephrol Sect, Chicago, IL 60637 USA
[3] Ohio State Univ, Dept Microbial Infect & Immun, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
T cell activation; Caspase-9; NF-kappa B; T-CELL-ACTIVATION; CBL-B; CASPASE; 8; LIGASE; PHOSPHORYLATION; DEGRADATION; APOPTOSIS; THRESHOLD; CLEAVAGE; PATHWAY;
D O I
10.1016/j.bbrc.2014.06.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been documented that caspase-8, a central player in apoptosis, is also crucial for TCR-mediated NF-kappa B activation. However, whether other caspases are also involved this process is unknown. In this report, we showed that in addition to caspase-8, caspase-9 is required for TCR-mediated NF-kappa B activation. Caspase-9 induces activation of PKC-theta, phosphorylation of Bcl10 and NF-kappa B activation in a caspase-3-dependent manner, but it appears that Bcl10 phosphorylation is uncoupled from NF-kappa B activation. Furthermore, caspase-8 lies upstream of caspase-9 during T cell activation. Therefore, TCR ligation elicits a caspase cascade involving caspase-8, caspase-9 and caspase-3 which initiates PKC-theta-dependent pathway leading to NF-kappa B activation and PKC-theta-independent Bcl10 phosphorylation which limits NF-kappa B activity. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:526 / 531
页数:6
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