Brasier A R, Li J, Wimbish K A
Department of Medicine, University of Texas Medical Branch, Galveston 77555-1060, USA.
Hypertension. 1996 Apr;27(4):1009-17. doi: 10.1161/01.hyp.27.4.1009.
Angiotensinogen encodes the only known precursor of angiotensin II, a critical regulator of the cardiovascular system. Transcriptional control of angiotensinogen in hepatocytes is an important regulator of circulating angiotensinogen concentrations. Angiotensinogen transcription is increased by the inflammatory cytokine tumor necrosis factor (TNF)-alpha by a nuclear factor-kappaB-like protein binding to an inducible enhancer called the acute-phase response element. By gel mobility shift assays, we observe two specific acute-phase response element-binding complexes, C1 and C2. The abundance of C2 is not changed by TNF treatment. In contrast, C1 is faintly detected in untreated cells, and its abundance increases by fivefold after stimulation. We identify the nuclear factor-kappaB subunits in these complexes using subunit-specific antibodies in the gel mobility "supershift" assay. The transcriptionally inert nuclear factor-kappaB DNA-binding subunit NF-kappaB1 is present in both control and stimulated hepatocyte nuclei. Its abundance changes weakly upon TNF stimulation. In contrast, the potent transactivating protein Rel A is not found in unstimulated hepatocyte nuclei and is recruited by TNF-alpha into the C1 DNA-binding complex. Overexpression of Rel A results in acute-phase response element transcription. Cotransfection of a chimeric GAL4-Rel A protein with GAL4 DNA-binding sites is a strategy that allows for selective study of Rel A. The GAL4:Rel A chimera is a TNF-alpha-inducible transactivator. Deletion of the amino-terminal 254 amino acids of Rel A produces a constitutive activator (that is no longer TNF-alpha inducible). The cytokine induction of Rel A, then, is mediated through its amino-terminal 254 amino acids. We conclude that Rel A:NF-kappaB1 is a crucial cytokine-inducible transcription factor complex regulating angiotensinogen gene synthesis in hepatocytes and may be involved in controlling the activity of the renin-angiotensin system.
血管紧张素原编码血管紧张素II唯一已知的前体,血管紧张素II是心血管系统的关键调节因子。肝细胞中血管紧张素原的转录控制是循环血管紧张素原浓度的重要调节因素。炎症细胞因子肿瘤坏死因子(TNF)-α通过一种与称为急性期反应元件的诱导性增强子结合的核因子-κB样蛋白增加血管紧张素原的转录。通过凝胶迁移率变动分析,我们观察到两种特异性急性期反应元件结合复合物,C1和C2。TNF处理后C2的丰度没有变化。相比之下,C1在未处理的细胞中检测不到,刺激后其丰度增加了五倍。我们在凝胶迁移“超迁移”分析中使用亚基特异性抗体鉴定这些复合物中的核因子-κB亚基。转录惰性的核因子-κB DNA结合亚基NF-κB1存在于对照和刺激的肝细胞核中。TNF刺激后其丰度变化微弱。相比之下,强效的反式激活蛋白Rel A在未刺激的肝细胞核中未发现,并且被TNF-α募集到C1 DNA结合复合物中。Rel A的过表达导致急性期反应元件转录。将嵌合的GAL4-Rel A蛋白与GAL4 DNA结合位点共转染是一种允许选择性研究Rel A的策略。GAL4:Rel A嵌合体是一种TNF-α诱导的反式激活因子。缺失Rel A的氨基末端254个氨基酸会产生一种组成型激活因子(不再受TNF-α诱导)。因此,Rel A的细胞因子诱导是通过其氨基末端254个氨基酸介导的。我们得出结论,Rel A:NF-κB1是一种关键的细胞因子诱导转录因子复合物,调节肝细胞中血管紧张素原基因的合成,可能参与控制肾素-血管紧张素系统的活性。