首页> 外文期刊>Microbial Pathogenesis >Expression of IL-6 and TNF-alpha in human alveolar epithelial cells is induced by invading, but not by adhering, Legionella pneumophila
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Expression of IL-6 and TNF-alpha in human alveolar epithelial cells is induced by invading, but not by adhering, Legionella pneumophila

机译:IL-6和TNF-α在人肺泡上皮细胞中的表达是通过侵袭而非粘附嗜肺军团菌来诱导的

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Legionella pnemophila causes atypical pneumonia in humans, especially in patients with chronic pulmonary diseases and underlying immunosuppression, and in elderly people. Several previous Studies have shown that L. pneumophila induced several inflammatory cytokines in murine macrophages, but little is known about cytokine induction by the bacterium in lung epithelial cells. In this study, we investigated the ability of L. pneumophila to stimulate the production of pro-inflammatory cytokines in the human A549 alveolar epithelial cell line during 24 h exposure to 106, 107, and 108 microbes. Infection of the wild L. pneumophila strain to A549 resulted in increased levels of interleukin-8 (IL-8), IL-6, and tumor necrosis factor alpha (TNF-alpha) mRNA, and also the secretion of their production into culture medium. In contrast, the level of mRNAs and proteins of IL-1beta and gamma interferon (IFN-gamma) remained unchanged and undetected, respectively. Production of IL-8, IL-6, and TNF-alpha in A549 decreased when an icmE multiplication-less mutant and the heat-killed L. pneumophila strain were inoculated. The treatment of cytochalasin D, which effectively inhibited invasion of L. pneumophila into A549, significantly reduced the production of IL-6 and TNF-alpha, but not IL-8. These results suggested that the induction and expression of IL-6 and TNF-alpha, in the human alveolar epithelial cells especially required intracellular signaling by L. pneumophila after invasion. Copyright 2004 Elsevier Ltd. All rights reserved.
机译:嗜肺军团菌会引起人类非典型肺炎,特别是在患有慢性肺部疾病和潜在免疫抑制的患者以及老年人中。先前的几项研究表明,嗜肺乳杆菌可在鼠巨噬细胞中诱导多种炎症细胞因子,但对于这种细菌在肺上皮细胞中诱导细胞因子的了解还很少。在这项研究中,我们调查了肺炎链球菌在暴露于106、107和108种微生物的24小时内刺激人A549肺泡上皮细胞系中促炎性细胞因子产生的能力。野生肺炎支原体菌株感染A549导致白细胞介素8(IL-8),IL-6和肿瘤坏死因子α(TNF-alpha)mRNA的水平升高,以及分泌它们的产物到培养基中。相反,IL-1β和γ干扰素(IFN-γ)的mRNA和蛋白质的水平分别保持不变和未被检测到。接种icmE无倍增突变体和热灭活的肺炎链球菌菌株后,A549中IL-8,IL-6和TNF-α的产生减少。细胞松弛素D的治疗有效地抑制了嗜肺乳杆菌入侵A549,显着降低了IL-6和TNF-α的产生,但没有降低IL-8的产生。这些结果表明,在人肺泡上皮细胞中IL-6和TNF-α的诱导和表达特别需要在侵袭后通过嗜肺乳杆菌的细胞内信号传导。版权所有2004 ElsevierLtd。保留所有权利。

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