Harhaj E W, Good L, Xiao G, Uhlik M, Cvijic M E, Rivera-Walsh I, Sun S C
Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, 500 University Drive, Hershey, Pennsylvania, PA 17033, USA.
Oncogene. 2000 Mar 9;19(11):1448-56. doi: 10.1038/sj.onc.1203445.
NF-kappa B plays a pivotal role in normal T-cell activation and may also mediate human T-cell leukemia virus (HTLV)-induced T-cell transformation. Activation of NF-kappa B by both T-cell costimulatory signals and the HTLV Tax protein involves stimulation of I kappa B kinase (IKK). As a genetic approach to dissect the intermediate steps involved in NF-kappa B activation in human T cells, we performed somatic cell mutagenesis to isolate signaling-defective mutant Jurkat T-cell lines. One of the mutant cell lines was shown to have a specific blockade in the IKK signaling pathway but remained competent in the c-Jun N-terminal kinase and MAP kinase pathways. Interestingly, this mutant cell line lacks expression of IKK gamma, a non-catalytic component of the IKK complex. Expression of exogenous IKK gamma in the mutant cells restored NF-kappa B activation by both the T-cell costimulation agents and Tax. These findings provide genetic evidence for the requirement of IKK gamma in NF-kappa B signaling triggered by both T-cell costimulatory signals and HTLV-I Tax protein.
核因子-κB在正常T细胞活化过程中起关键作用,并且也可能介导人类T细胞白血病病毒(HTLV)诱导的T细胞转化。T细胞共刺激信号和HTLV Tax蛋白对核因子-κB的激活均涉及IκB激酶(IKK)的刺激。作为剖析人类T细胞中核因子-κB激活所涉及中间步骤的遗传学方法,我们进行了体细胞诱变以分离信号缺陷型突变Jurkat T细胞系。其中一个突变细胞系显示在IKK信号通路中有特异性阻断,但在c-Jun N末端激酶和丝裂原活化蛋白激酶通路中仍具有活性。有趣的是,该突变细胞系缺乏IKKγ的表达,IKKγ是IKK复合物的非催化成分。在突变细胞中外源性表达IKKγ可恢复T细胞共刺激剂和Tax对核因子-κB的激活。这些发现为IKKγ在T细胞共刺激信号和HTLV-I Tax蛋白触发的核因子-κB信号传导中的需求提供了遗传学证据。