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表皮葡萄球菌(94B080)和金黄色葡萄球菌(90B083)刺激后支气管上皮细胞中 ENaC、CFTR 和 iNOS 表达的调节。

Modulation of ENaC, CFTR, and iNOS expression in bronchial epithelial cells after stimulation with Staphylococcus epidermidis (94B080) and Staphylococcus aureus (90B083).

机构信息

School of Health and Medical Sciences, Örebro University, Örebro, Sweden.

出版信息

APMIS. 2013 Sep;121(9):814-26. doi: 10.1111/apm.12138. Epub 2013 Jul 24.

Abstract

Bacteria affect the respiratory epithelium, which is covered by airway surface liquid (ASL) and mucus. Ion concentrations in the ASL are determined by the cystic fibrosis transmembrane conductance regulator (CFTR) and the epithelial Na(+) channel (ENaC). Neonatal sepsis is a major risk factor for subsequent pulmonary disease in preterm newborns. Predominating are coagulase-negative staphylococci (e.g., Staphylococccus epidermidis and Staphylococccus aureus). The aim of this study was to investigate modulation of CFTR, ENaC, mucins, proinflammatory cytokines, and inducible nitric oxide synthase (iNOS) in respiratory epithelial cells after S. epidermidis 94B080 and S. aureus 90B083 exposure. Bronchial epithelial cells were incubated with S. epidermidis 94B080 and S. aureus 90B083 (neonatal blood isolates) for 1-36 h. Expression of CFTR, ENaC, iNOS, and mucins was analyzed by real-time PCR and Western blotting. Release of cytokines was analyzed by ELISA, and production of NO by the Griess assay. Expression of CFTR significantly decreased after 36 h incubation with S. epidermidis and more prominently with S. aureus, whereas S. epidermidis caused a significant increase in the expression of β- and γ-ENaC. Expression of iNOS increased, but NO was not detected. Both staphylococci caused a decrease in the intracellular Ca(2+) concentration. S. aureus induced increased secretion of IL-6, IL-8, and transforming nuclear factor (TNF)-α in a time-dependent manner as compared with S. epidermidis. In conclusion, expression of ENaC, CFTR, and iNOS is modulated by exposure to S. aureus 90B083 and S. epidermidis 94B080. S. aureus is more potent in causing release of IL-6, IL-8, and TNF-α by bronchial epithelial cells as compared with S. epidermidis. The mRNA expression for the mucus proteins MUC2, MUC5AC, and MUC5B could not be measured, neither in the presence nor in the absence of bacteria.

摘要

细菌会影响覆盖在气道表面液体 (ASL) 和黏液上的呼吸上皮细胞。ASL 中的离子浓度由囊性纤维化跨膜电导调节因子 (CFTR) 和上皮钠离子通道 (ENaC) 决定。新生儿败血症是早产儿随后发生肺部疾病的主要危险因素。主要病原体为凝固酶阴性葡萄球菌(例如表皮葡萄球菌和金黄色葡萄球菌)。本研究旨在研究表皮葡萄球菌 94B080 和金黄色葡萄球菌 90B083 暴露后,呼吸上皮细胞中 CFTR、ENaC、粘蛋白、促炎细胞因子和诱导型一氧化氮合酶 (iNOS) 的调节作用。用表皮葡萄球菌 94B080 和金黄色葡萄球菌 90B083(新生儿血液分离株)孵育支气管上皮细胞 1-36 小时。通过实时 PCR 和 Western blot 分析 CFTR、ENaC、iNOS 和粘蛋白的表达。通过 ELISA 分析细胞因子的释放,通过 Griess 测定法分析 NO 的产生。与表皮葡萄球菌相比,与金黄色葡萄球菌孵育 36 小时后 CFTR 的表达明显降低,而表皮葡萄球菌则显著增加了β和γ-ENaC 的表达。iNOS 的表达增加,但未检测到 NO。两种葡萄球菌均导致细胞内 Ca(2+)浓度降低。与表皮葡萄球菌相比,金黄色葡萄球菌可诱导 IL-6、IL-8 和转化核因子 (TNF)-α 的分泌呈时间依赖性增加。总之,暴露于金黄色葡萄球菌 90B083 和表皮葡萄球菌 94B080 可调节 ENaC、CFTR 和 iNOS 的表达。与表皮葡萄球菌相比,金黄色葡萄球菌更能引起支气管上皮细胞释放 IL-6、IL-8 和 TNF-α。在存在或不存在细菌的情况下,均无法测量粘蛋白蛋白 MUC2、MUC5AC 和 MUC5B 的 mRNA 表达。

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