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首页> 外文期刊>In vivo. >Establishment of an in vitro model using NR8383 cells and mycobacterium bovis calmette-guerin that mimics a chronic infection of mycobacterium tuberculosis.
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Establishment of an in vitro model using NR8383 cells and mycobacterium bovis calmette-guerin that mimics a chronic infection of mycobacterium tuberculosis.

机译:使用NR8383细胞和模拟结核分枝杆菌慢性感染的牛分枝杆菌-牛尿蛋白建立体外模型。

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BACKGROUND: Mycobacterium tuberculosis infection affects one-third of the world's population and causes the death of three million people each year. To clarify details of M. tuberculosis survival strategies, it is important to establish a suitable in vitro model that mimics a chronic infection in alveolar macrophages by M. tuberculosis. For this reason, we established a new in vitro model using a rat alveolar macrophage cell line, NR8383. MATERIALS AND METHODS: Basic characteristics, including phagocytotic ability and production of nitrogen oxide and tumor necrosis factor in response to several stimuli, of NR8383 cells were compared with those of primary alveolar macrophages. The course after phagocytosis of live or killed M. bovis bacilli Calmette-Guerin (BCG) was examined over 21 days using NR8383 cells as the host. RESULTS: The characteristics that have been examined to date were nearly the same for both primary alveolar macrophage and NR8383 cells. Live BCG phagocytosed by NR8383 cells had successfully begun to grow in the cells within 7 days, while killed BCG were almost completely destroyed by 21 days. CONCLUSION: BCG-infected NR8383 cells are potentially a suitable in vitro model that mimics a chronic infection with M tuberculosis.
机译:背景:结核分枝杆菌感染影响世界三分之一的人口,每年造成三百万人死亡。为了阐明结核分枝杆菌生存策略的细节,重要的是建立一个合适的体外模型,以模拟结核分枝杆菌对肺泡巨噬细胞的慢性感染。因此,我们使用大鼠肺泡巨噬细胞系NR8383建立了新的体外模型。材料与方法:将NR8383细胞与原发性肺泡巨噬细胞的基本特征,包括吞噬能力以及对多种刺激的反应产生的氮氧化物和肿瘤坏死因子的产生。使用NR8383细胞作为宿主,在21天的时间内检查了活的或杀死的牛分枝杆菌杆菌Calmette-Guerin(BCG)的吞噬过程。结果:迄今为止,原发性肺泡巨噬细胞和NR8383细胞的特征几乎相同。被NR8383细胞吞噬的活BCG已在7天内成功开始在细胞中生长,而被杀死的BCG在21天内几乎被完全破坏。结论:BCG感染的NR8383细胞可能是一种适合的体外模型,可模拟M结核的慢性感染。

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