Mori N, Oishi K, Sar B, Mukaida N, Nagatake T, Matsushima K, Yamamoto N
Department of Preventive Medicine and AIDS Research, Institute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.
Infect Immun. 1999 Aug;67(8):3872-8. doi: 10.1128/IAI.67.8.3872-3878.1999.
Persistent infection with Pseudomonas aeruginosa increases interleukin-8 (IL-8) levels and causes dense neutrophil infiltrations in the airways of patients with chronic airway diseases. Recently, we have reported that nitrite reductase from P. aeruginosa induces the production of IL-8 in respiratory cells, including bronchial epithelial cells. To determine the molecular mechanism(s) of nitrite reductase-induced IL-8 expression in respiratory cells, A549 epithelial cells were transfected with plasmids containing serial deletions of the 5'-flanking region of the IL-8 gene and then exposed to nitrite reductase. Nitrite reductase significantly enhanced IL-8 gene promoter-driven reporter activity. This increased IL-8 gene expression was inhibited by mutating the nuclear factor-kappaB (NF-kappaB) binding element. Nitrite reductase enhanced nuclear localization of the NF-kappaB binding complex. Furthermore, nitrite reductase induced the degradation of IkappaBalpha, the major cytoplasmic inhibitor of NF-kappaB, and the expression of IkappaBalpha mRNA. These data support the critical role of the activation of NF-kappaB in nitrite reductase-induced IL-8 gene expression in airway epithelium.
铜绿假单胞菌的持续感染会增加白细胞介素-8(IL-8)水平,并导致慢性气道疾病患者气道中出现大量中性粒细胞浸润。最近,我们报道了铜绿假单胞菌的亚硝酸还原酶可诱导包括支气管上皮细胞在内的呼吸道细胞产生IL-8。为了确定亚硝酸还原酶诱导呼吸道细胞中IL-8表达的分子机制,将含有IL-8基因5'侧翼区系列缺失的质粒转染至A549上皮细胞,然后使其暴露于亚硝酸还原酶。亚硝酸还原酶显著增强了IL-8基因启动子驱动的报告基因活性。通过突变核因子-κB(NF-κB)结合元件,这种增加的IL-8基因表达受到抑制。亚硝酸还原酶增强了NF-κB结合复合物的核定位。此外,亚硝酸还原酶诱导了NF-κB主要胞质抑制剂IκBα的降解以及IκBα mRNA的表达。这些数据支持了NF-κB激活在亚硝酸还原酶诱导气道上皮细胞中IL-8基因表达中的关键作用。