Mastronarde J G, Monick M M, Mukaida N, Matsushima K, Hunninghake G W
Pulmonary Division, Veterans Affairs Medical Center, Portland, Oregon, USA.
J Infect Dis. 1998 May;177(5):1275-81. doi: 10.1086/515279.
The role of "oxidant-sensitive" transcription factors activator protein (AP)-1, nuclear factor (NF)-kappaB, and NF-IL6 in respiratory syncytial virus (RSV)-induced interleukin (IL)-8 gene expression in A549 epithelial cells was evaluated. RSV infection resulted in increased binding of each of these transcription factors. Transfection of A549 cells with plasmids containing serial truncations of the 5'-flanking region of the IL-8 gene revealed a positive cooperative effect of the binding sites for AP-1 and NF-kappaB. Mutation of either region markedly diminished responsiveness of the promoter to RSV. Mutation of the NF-IL6 site had minimal effect in the presence of intact binding sites for NF-kappaB and AP-1. The antioxidants NAC (N-acetylcysteine), DMSO, and DMPO (5,5-dimethyl-1-pyrroline N-oxide) did not inhibit RSV-induced binding of NF-kappaB; however, binding of AP-1 and NF-IL6 was inhibited. These observations suggest that AP-1 may be the preferred transcription factor (over NF-IL6) for cooperative interaction with NF-kappaB in RSV-induced IL-8 production.
评估了“氧化还原敏感型”转录因子激活蛋白(AP)-1、核因子(NF)-κB和NF-IL6在呼吸道合胞病毒(RSV)诱导A549上皮细胞白细胞介素(IL)-8基因表达中的作用。RSV感染导致这些转录因子的结合增加。用含有IL-8基因5'侧翼区系列截短片段的质粒转染A549细胞,揭示了AP-1和NF-κB结合位点的正协同效应。任一区域的突变均显著降低启动子对RSV的反应性。在NF-κB和AP-1的结合位点完整的情况下,NF-IL6位点的突变影响最小。抗氧化剂N-乙酰半胱氨酸(NAC)、二甲基亚砜(DMSO)和5,5-二甲基-1-吡咯啉N-氧化物(DMPO)不抑制RSV诱导的NF-κB结合;然而,AP-1和NF-IL6的结合受到抑制。这些观察结果表明,在RSV诱导的IL-8产生中,AP-1可能是与NF-κB协同相互作用的首选转录因子(优于NF-IL6)。