Mastronarde J G, He B, Monick M M, Mukaida N, Matsushima K, Hunninghake G W
Division of Pulmonary, Critical Care, University of Iowa College of Medicine, Iowa City, USA.
J Infect Dis. 1996 Aug;174(2):262-7. doi: 10.1093/infdis/174.2.262.
Respiratory syncytial virus (RSV) preferentially infects respiratory epithelium and is an important cause of lower respiratory tract infections in young children. RSV induces the production of interleukin (IL)-8 in airway epithelial cells; however, the mechanism of this induction is not known. To define the mechanism by which RSV induces IL-8 gene activation, A549 epithelial cells were transfected with plasmids containing serial deletions of the 5'-flanking region of the IL-8 gene and then exposed to RSV for 24 h. A positive cooperative effect of the binding sites for the transcription factors, nuclear factor (NF)-kappa B and NF-IL-6, was observed. Mutations in either region abates responsiveness of the promoter to RSV infection. RSV also increases activation of the NF-kappa B and NF-IL-6 transcription factors. These data suggest that RSV may increase IL-8 production in airway epithelium partly via activation of the transcription factors NF-kappa B and NF-IL-6.
呼吸道合胞病毒(RSV)优先感染呼吸道上皮,是幼儿下呼吸道感染的重要病因。RSV诱导气道上皮细胞产生白细胞介素(IL)-8;然而,这种诱导机制尚不清楚。为了确定RSV诱导IL-8基因激活的机制,将含有IL-8基因5'侧翼区系列缺失的质粒转染A549上皮细胞,然后使其暴露于RSV 24小时。观察到转录因子核因子(NF)-κB和NF-IL-6结合位点的正协同效应。任一区域的突变都会减弱启动子对RSV感染的反应性。RSV还增加NF-κB和NF-IL-6转录因子的激活。这些数据表明,RSV可能部分通过激活转录因子NF-κB和NF-IL-6来增加气道上皮中IL-8的产生。