Page Kristen, Hughes Valerie S, Odoms Kelli K, Dunsmore Katherine E, Hershenson Marc B
Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, ML7006, Cincinnati, OH 45229, USA.
Am J Respir Cell Mol Biol. 2005 Mar;32(3):225-31. doi: 10.1165/rcmb.2004-0231OC. Epub 2004 Dec 2.
German cockroach extract synergistically regulates tumor necrosis factor-alpha (TNF-alpha)-induced interleukin (IL)-8 expression in human airway epithelial cells. The IL-8 promoter contains nuclear factor (NF)-kappaB, activating protein (AP)-1, and NF for IL-6 (NF-IL6) transcription factor binding regions. Because cockroach extract activates extracellular regulated kinase (ERK), a known activator of AP-1 and NF-IL6, we focused on the regulation of these transcription factors. Although TNF-alpha and cockroach extract both increased AP-1 translocation, mutation of the AP-1 site in the context of the wild-type promoter had no effect on cockroach extract-induced synergy. Mutation of the NF-IL6 site in the context of the wild-type IL-8 promoter, or overexpression of a dominant-negative NF-IL6 mutant, each abolished cockroach extract-induced synergy. Cockroach extract induced NF-IL6 translocation and DNA binding, an effect that was further increased in the presence of TNF-alpha. Cockroach extract-induced regulation of NF-IL6 was due to active serine proteases in the extract as well as activation of protease activated receptor (PAR)-2, but not PAR-1. Chemical inhibition of ERK also attenuated cockroach extract-induced NF-IL6-DNA binding. We conclude that proteases in German cockroach extract regulate PAR-2 and ERK to increase NF-IL6 activity and synergistically regulate TNF-alpha-induced IL-8 promoter activity in human airway epithelium.
德国小蠊提取物协同调节肿瘤坏死因子-α(TNF-α)诱导的人气道上皮细胞中白细胞介素(IL)-8的表达。IL-8启动子包含核因子(NF)-κB、激活蛋白(AP)-1和IL-6核因子(NF-IL6)转录因子结合区域。由于蟑螂提取物可激活细胞外调节激酶(ERK),而ERK是已知的AP-1和NF-IL6激活剂,因此我们重点研究了这些转录因子的调节作用。尽管TNF-α和蟑螂提取物均可增加AP-1的易位,但在野生型启动子背景下AP-1位点的突变对蟑螂提取物诱导的协同作用没有影响。在野生型IL-8启动子背景下NF-IL6位点的突变,或显性负性NF-IL6突变体的过表达,均消除了蟑螂提取物诱导的协同作用。蟑螂提取物诱导NF-IL6易位和DNA结合,在TNF-α存在的情况下,这种作用会进一步增强。蟑螂提取物诱导的NF-IL6调节是由于提取物中的活性丝氨酸蛋白酶以及蛋白酶激活受体(PAR)-2的激活,而非PAR-1。ERK的化学抑制也减弱了蟑螂提取物诱导的NF-IL6与DNA的结合。我们得出结论,德国小蠊提取物中的蛋白酶调节PAR-2和ERK以增加NF-IL6活性,并协同调节TNF-α诱导的人气道上皮细胞中IL-8启动子的活性。