Li Yi-Dan, Ye Bu-Qing, Zheng Sheng-Xi, Wang Jin-Tao, Wang Jian-Guo, Chen Ming, Liu Ji-Guo, Pei Xin-Hui, Wang Li-Jing, Lin Zhi-Xin, Gupta Kalpna, Mackman Nigel, Slungaard Arne, Key Nigel S, Geng Jian-Guo
Laboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, The Graduate School of Chinese Academy of Sciences, CAS, Shanghai 200031, China.
J Biol Chem. 2009 Feb 13;284(7):4473-83. doi: 10.1074/jbc.M806010200. Epub 2008 Dec 18.
NF-kappaB transcription factors regulate the expression of tissue factor (TF), a principal initiator of the coagulation cascade. Dominant among them is the p50/p65 heterodimer. Here we report that Andrographolide (Andro; a p50 inhibitor) and genetic deletion of p50 attenuated TF activity in stimulated endothelial cells and monocytes/macrophages. Results of the electrophoretic mobility "supershift" assay and chromatin immunoprecipitation demonstrated the direct interaction of the p50/p65 heterodimer with the NF-kappaB site of the human TF promoter. Andro-treated and p50 null mice both exhibited blunted TF expression and reduced venous thrombosis, which were recapitulated by an anti-murine TF antibody in vivo. Our findings thus indicate that regulation of TF by NF-kappaB transcription factor p50 is essential for the pathogenesis of deep vein thrombosis and suggest that specific inhibitors of p50, such as Andro, may be therapeutically valuable for preventing and perhaps treating venous thrombosis.
核因子-κB转录因子调节组织因子(TF)的表达,组织因子是凝血级联反应的主要启动因子。其中占主导地位的是p50/p65异二聚体。在此我们报告,穿心莲内酯(Andro;一种p50抑制剂)和p50基因缺失减弱了刺激的内皮细胞和单核细胞/巨噬细胞中的TF活性。电泳迁移率“超迁移”分析和染色质免疫沉淀结果证明了p50/p65异二聚体与人TF启动子的核因子-κB位点直接相互作用。经Andro处理的小鼠和p50基因敲除小鼠均表现出TF表达减弱和静脉血栓形成减少,这在体内被抗小鼠TF抗体所重现。因此,我们的研究结果表明,核因子-κB转录因子p50对TF的调节对于深静脉血栓形成的发病机制至关重要,并表明p50的特异性抑制剂,如Andro,可能在预防甚至治疗静脉血栓形成方面具有治疗价值。