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比较源自水生环境中大肠杆菌和本土细菌的脂多糖对人体细胞引发的炎症反应。

Comparison of inflammatory responses in human cells caused by lipopolysaccharides from Escherichia coli and from indigenous bacteria in aquatic environment.

机构信息

Department of Global Ecology, Graduate School of Global Environmental Studies, Kyoto University, Nishikyo-ku, Kyoto, Japan.

出版信息

J Environ Sci Health A Tox Hazard Subst Environ Eng. 2012;47(13):1966-74. doi: 10.1080/10934529.2012.695254.

Abstract

The endotoxic activities of lipopolysaccharides (LPSs) in water samples are usually determined using a Limulus amoebocyte lysate (LAL) assay, but it is known that the determined activities do not always represent their inflammatory potency in humans. In this investigation, the inflammatory responses in three different human cells stimulated with Escherichia coli LPS, keratinocyte, CD14(+) monocyte, and THP-1, were compared using cytokine secretion as biomarkers to develop novel in vitro assay systems for detecting changes in inflammatory potencies of endotoxins in aquatic environment. Only THP-1 with 6-h stimulation showed dose-dependent responses in the range of normal endotoxin levels in aquatic environment. Then, the inflammatory potency of environmental LPS, which was purified from river water, was tested using THP-1. The levels and patterns of cytokine secretion after the environmental LPS stimulation were completely different from E. coli LPS. Interleukin 8 (IL-8) secretions after the environmental LPS stimulation were approximately 10-fold higher than those after E. coli LPS stimulation. The environmental LPS also induced much higher levels of TNF-α secretions in THP-1. These results suggest that a diversity of LPS structures in aquatic environment could contribute to stronger and different inflammatory responses. This investigation indicated that the proposed THP-1 assay system could be useful for detecting the changes in inflammatory potencies caused by aquatic bacteria.

摘要

水样中的脂多糖 (LPS) 的内毒素活性通常使用鲎变形细胞溶解物 (LAL) 测定法来测定,但已知所测定的活性并不总是代表其在人类中的炎症效力。在这项研究中,使用细胞因子分泌作为生物标志物比较了三种不同的人细胞(角质形成细胞、CD14(+)单核细胞和 THP-1)在大肠杆菌 LPS 刺激下的炎症反应,以开发用于检测水生环境中内毒素炎症效力变化的新型体外检测系统。只有经过 6 小时刺激的 THP-1 在水生环境中正常内毒素水平范围内显示出剂量依赖性反应。然后,使用 THP-1 测试了从河水纯化的环境 LPS 的炎症效力。环境 LPS 刺激后的细胞因子分泌水平和模式与大肠杆菌 LPS 完全不同。环境 LPS 刺激后的白细胞介素 8 (IL-8) 分泌量比大肠杆菌 LPS 刺激后的分泌量高约 10 倍。环境 LPS 还在 THP-1 中诱导了更高水平的 TNF-α 分泌。这些结果表明,水生环境中 LPS 结构的多样性可能导致更强和不同的炎症反应。本研究表明,所提出的 THP-1 测定系统可用于检测由水生细菌引起的炎症效力变化。

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