核因子 kappaB 活化的体内生物发光成像:研究活体小鼠炎症和氧化应激的重要模型

Hong Zhu, Zhenquan Jia, Michael A Trush, Y Robert Li
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引用次数: 0

摘要

核因子卡巴(NF-κB)是一种对氧化还原反应敏感的转录因子,在炎症和其他生物功能中起着至关重要的作用。这篇《ROS 协议》文章介绍了一种体内生物发光成像检测方法,利用携带 NF-κB 反应元件-荧光素酶报告基因(NF-κB-RE-Luc)的市售转基因小鼠来评估 NF-κB 的活化情况。利用高灵敏度的 Berthold NightOwl LB981 体内生物发光成像系统,我们能够观察到活体小鼠在基础条件下的 NF-κB 激活情况,这表明 NF-κB 构成性激活是其基本生物学特性的一部分。用脂多糖(LPS)处理小鼠会导致生物发光急剧增加,这证明了该模型在评估炎症压力方面的有效性。用核因子 E-2 相关因子 2(Nrf2)的激活剂 3H-1,2-二硫代-3-硫酮(D3T)处理小鼠后,活体小鼠的 NF-κB 基础激活和 LPS 诱导的激活均显著减少,这表明该模型在评估抑制 NF-κB 激活和炎症应激的药物疗效方面具有重要价值。本文详细介绍了这一宝贵模型的操作规程,并讨论了它在研究涉及炎症和氧化应激机制的疾病状况以及评估针对 NF-κB 信号的疾病干预治疗模式方面的潜在用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In Vivo Bioluminescence Imaging of Nuclear Factor kappaB Activation: A Valuable Model for Studying Inflammatory and Oxidative Stress in Live Mice.

In Vivo Bioluminescence Imaging of Nuclear Factor kappaB Activation: A Valuable Model for Studying Inflammatory and Oxidative Stress in Live Mice.

In Vivo Bioluminescence Imaging of Nuclear Factor kappaB Activation: A Valuable Model for Studying Inflammatory and Oxidative Stress in Live Mice.

In Vivo Bioluminescence Imaging of Nuclear Factor kappaB Activation: A Valuable Model for Studying Inflammatory and Oxidative Stress in Live Mice.

The nuclear factor kappaB (NF-κB) is a redox-sensitive transcription factor that plays a critical role in inflammation among other biological functions. This ROS Protocol article describes an in vivo bioluminescence imaging assay for assessing NF-κB activation using the commercially available transgenic mice carrying NF-κB response element-luciferase reporter gene (NF-κB-RE-Luc). Using the highly sensitive Berthold NightOwl LB981 in vivo bioluminescence imaging system, we are able to visualize the NF-κB activation in live mice under basal conditions, suggesting constitutive activation of NF-κB as a part of its fundamental biology. Treatment of mice with lipopolysaccharides (LPS) results in a drastic increase in bioluminescence, proving the validity of the model in assessing inflammatory stress. Treatment of mice with 3H-1,2-dithiole-3-thione (D3T), an activator of nuclear factor E-2 related factor 2 (Nrf2), led to a significant reduction in both basal and LPS-induced activation of NF-κB in the live mice, suggesting a value of this model in assessing drug efficacy in suppressing NF-κB activation and inflammatory stress. The protocols of this valuable model are detailed in this article along with a discussion of its potential use in studying disease conditions involving inflammatory and oxidative stress mechanisms and in assessing therapeutic modalities targeting the NF-κB signaling for disease intervention.

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