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用于分析Nod1和Nod2激活的基于细胞的报告基因检测

Cell-based reporter assay to analyze activation of Nod1 and Nod2.

作者信息

Zurek Birte, Bielig Harald, Kufer Thomas A

机构信息

Molecular Innate Immunobiology Group, Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany.

出版信息

Methods Mol Biol. 2011;748:107-19. doi: 10.1007/978-1-61779-139-0_7.

Abstract

Nod1 and Nod2 are pattern recognition receptors of the mammalian innate immune system. They respond to bacterial peptidoglycan fragments and are implicated in host defense against a variety of -different bacterial pathogens. Recent studies furthermore support additional functions of these proteins in the control of adaptive immune responses and intestinal homeostasis. Activation of Nod1 and Nod2 by their cognate elicitors triggers inflammatory responses driven by the activation of NF-κB and MAPK pathways. In this chapter, we describe a quick and reliable cell-based assay using a luciferase reporter to measure Nod1- and Nod2-mediated NF-κB activation. The described protocol was successfully applied to analyze the influences of overexpressed proteins and siRNA-mediated knock-down to provide new insights into the regulation of Nod1/2-specific signaling pathways. Furthermore, this method is well suited for downscaling to high-throughput screening applications.

摘要

Nod1和Nod2是哺乳动物先天免疫系统的模式识别受体。它们对细菌肽聚糖片段作出反应,并参与宿主对多种不同细菌病原体的防御。此外,最近的研究支持这些蛋白质在适应性免疫反应控制和肠道稳态中的其他功能。Nod1和Nod2被其同源诱导物激活会触发由NF-κB和MAPK途径激活驱动的炎症反应。在本章中,我们描述了一种使用荧光素酶报告基因来测量Nod1和Nod2介导的NF-κB激活的快速可靠的基于细胞的检测方法。所描述的方案已成功应用于分析过表达蛋白和siRNA介导的敲低的影响,以提供对Nod1/2特异性信号通路调控的新见解。此外,该方法非常适合缩放到高通量筛选应用。

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