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建立能够检测 NF-κB 介导的免疫调节活性的报告平台。

Establishment of reporter platforms capable of detecting NF-κB mediated immuno-modulatory activity.

机构信息

Institute of Food Science and Technology, National Taiwan University , Taipei, Taiwan, R.O.C.

出版信息

J Agric Food Chem. 2013 Dec 26;61(51):12582-7. doi: 10.1021/jf404887u. Epub 2013 Dec 17.

Abstract

Cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) are transcriptional targets of nuclear factor kappa B (NF-κB) that are involved in inflammatory responses. The aim of this study is to develop a method for efficiently detecting inflammation modulatory activities. Here we established RAW264.7 macrophage cells stably expressing a luciferase reporter gene directed by iNOS or COX-2 promoter. Lipopolysaccharide (LPS) treatment stimulated the luciferase activity which paralleled with increased iNOS and COX-2 mRNA levels determined by RT-q-PCR. The LPS-stimulated luciferase activity was blocked by NF-κB inhibitor CAPE and by nobiletin, an anti-inflammatory natural product from citrus peels. We have applied the platforms to screen various mushroom species; analysis by scatter plot revealed a strong correlation to the results obtained by ELISA-based detection of TNF-α. Together we have established luciferase reporter systems sensitive to NF-κB-dependent iNOS and COX-2 activation, which provides an alternative screening method for identifying food components with immune-modulatory activities.

摘要

环氧化酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)是核因子κB(NF-κB)的转录靶标,参与炎症反应。本研究旨在开发一种有效检测炎症调节活性的方法。在这里,我们建立了稳定表达由 iNOS 或 COX-2 启动子指导的荧光素酶报告基因的 RAW264.7 巨噬细胞。脂多糖(LPS)处理刺激荧光素酶活性,与通过 RT-qPCR 确定的 iNOS 和 COX-2 mRNA 水平的增加平行。NF-κB 抑制剂 CAPE 和来自柑橘皮的抗炎天然产物诺必灵阻断 LPS 刺激的荧光素酶活性。我们已经将这些平台应用于筛选各种蘑菇物种;通过散点图分析显示与基于 ELISA 检测 TNF-α 的结果具有很强的相关性。我们共同建立了对 NF-κB 依赖性 iNOS 和 COX-2 激活敏感的荧光素酶报告系统,为鉴定具有免疫调节活性的食物成分提供了一种替代筛选方法。

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