Schreck R, Grassmann R, Fleckenstein B, Baeuerle P A
Laboratory for Molecular Biology, Ludwig-Maximilians University Munich, Martinsried, Germany.
J Virol. 1992 Nov;66(11):6288-93. doi: 10.1128/JVI.66.11.6288-6293.1992.
Oxygen radical scavengers, such as dithiocarbamates and cysteine derivatives, inhibit activation of the ubiquitous transcription factor nuclear factor kappa B (NF-kappa B) after treatment of cells with tumor necrosis factor, phorbol ester, and interleukin-1. An involvement of oxygen radicals was more directly evident from the induction of NF-kappa B by low concentrations of H2O2 and the demonstration that cells stimulated with various NF-kappa B inducers release H2O2 and superoxide. In this study, we used the antioxidant pyrrolidine dithiocarbamate (PDTC) to investigate whether the activation of NF-kappa B by the viral transactivator Tax from human T-cell leukemia virus type I also depends on the production of reactive oxygen intermediates. The Tax-induced activation of the DNA-binding activity of NF-kappa B in Jurkat T cells was potently suppressed by micromolar concentrations of PDTC. Within the same concentration range, PDTC and two other dithiocarbamates also strongly interfered with transactivation of the long terminal repeat (LTR) of human immunodeficiency virus type 1 by Tax but had no effect on transactivation of the same LTR by Tat. Transactivation of the human T-cell leukemia virus type I LTR by Tax was also barely influenced. Tax seems to activate NF-kappa B by a mechanism shared with all other inducers of NF-kappa B tested so far. It appears that one of the pleiotropic activities of Tax leads to an enhanced production of oxygen radicals that are required for activation of NF-kappa B.
氧自由基清除剂,如二硫代氨基甲酸盐和半胱氨酸衍生物,在细胞经肿瘤坏死因子、佛波酯和白细胞介素-1处理后,可抑制普遍存在的转录因子核因子κB(NF-κB)的激活。低浓度的过氧化氢可诱导NF-κB,并且有证据表明用各种NF-κB诱导剂刺激的细胞会释放过氧化氢和超氧化物,这更直接地证明了氧自由基的参与。在本研究中,我们使用抗氧化剂吡咯烷二硫代氨基甲酸盐(PDTC)来研究人T细胞白血病病毒I型的病毒反式激活因子Tax对NF-κB的激活是否也依赖于活性氧中间体的产生。微摩尔浓度的PDTC可有效抑制Tax诱导的Jurkat T细胞中NF-κB的DNA结合活性的激活。在相同浓度范围内,PDTC和其他两种二硫代氨基甲酸盐也强烈干扰Tax对人免疫缺陷病毒1型长末端重复序列(LTR)的反式激活,但对Tat对同一LTR的反式激活没有影响。Tax对人T细胞白血病病毒I型LTR的反式激活也几乎没有受到影响。Tax似乎通过一种与迄今为止测试的所有其他NF-κB诱导剂共有的机制激活NF-κB。看来Tax的多效性活动之一导致氧自由基产生增加,而氧自由基是激活NF-κB所必需的。