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Crystalline Pseudomonas cytochrome oxidase. I. Enzymic properties with special reference to the biological specificity.结晶假单胞菌细胞色素氧化酶。I. 酶学性质,特别涉及生物学特异性。
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Nitrite reductase from Pseudomonas aeruginosa released by antimicrobial agents and complement induces interleukin-8 production in bronchial epithelial cells.由抗菌剂和补体释放的铜绿假单胞菌亚硝酸还原酶可诱导支气管上皮细胞产生白细胞介素-8。
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Identification of tumor-specific paclitaxel (Taxol)-responsive regulatory elements in the interleukin-8 promoter.白细胞介素-8启动子中肿瘤特异性紫杉醇(泰素)反应性调控元件的鉴定。
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Nitrite reductase from Pseudomonas aeruginosa induces inflammatory cytokines in cultured respiratory cells.铜绿假单胞菌亚硝酸还原酶可诱导培养的呼吸道细胞产生炎性细胞因子。
Infect Immun. 1997 Jul;65(7):2648-55. doi: 10.1128/iai.65.7.2648-2655.1997.
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Human cytomegalovirus induces interleukin-8 production by a human monocytic cell line, THP-1, through acting concurrently on AP-1- and NF-kappaB-binding sites of the interleukin-8 gene.人巨细胞病毒通过同时作用于白细胞介素-8基因的AP-1和NF-κB结合位点,诱导人单核细胞系THP-1产生白细胞介素-8。
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Transactivation of the interleukin-1alpha promoter by human T-cell leukemia virus type I and type II Tax proteins.I型和II型人类T细胞白血病病毒Tax蛋白对白细胞介素-1α启动子的反式激活作用
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转录因子核因子-κB在铜绿假单胞菌亚硝酸还原酶对呼吸道上皮细胞白细胞介素-8基因表达调控中的重要作用。

Essential role of transcription factor nuclear factor-kappaB in regulation of interleukin-8 gene expression by nitrite reductase from Pseudomonas aeruginosa in respiratory epithelial cells.

作者信息

Mori N, Oishi K, Sar B, Mukaida N, Nagatake T, Matsushima K, Yamamoto N

机构信息

Department of Preventive Medicine and AIDS Research, Institute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.

出版信息

Infect Immun. 1999 Aug;67(8):3872-8. doi: 10.1128/IAI.67.8.3872-3878.1999.

DOI:10.1128/IAI.67.8.3872-3878.1999
PMID:10417151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC96667/
Abstract

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.

摘要

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。