体内免疫自旋捕获:氧化应激的成像足迹

Q1 Health Professions
Nicholas K.H. Khoo, Nadiezhda Cantu-Medellin, Claudette St. Croix, Eric E. Kelley
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引用次数: 13

摘要

大量的疾病过程与活性物质形成的升高以及与生物分子的相关反应有关,这些反应会改变细胞信号,诱导明显的损伤,并促进组织功能障碍。不幸的是,组织中活性物质的有效检测存在一些问题,这些问题极大地限制了验证物质身份、建立准确浓度和确定生产解剖部位的能力。这些缺点表明迫切需要新的方法来更精确地评估体内反应性物种的产生。在此,我们描述了一种体内免疫自旋捕获方法,该方法通过检测氧化剂与生物分子反应形成稳定的、免疫可检测的氮分子-生物分子加合物所产生的自由基来间接评估氧化剂水平。该过程将电子顺磁共振自旋阱的反应性和灵敏度与共聚焦成像的分辨率结合起来,通过检测产生的自由基形成来可视化细胞和组织氧化的程度和生产的解剖部位。©2015 by John Wiley &儿子,Inc。
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 Immuno-Spin Trapping: Imaging the Footprints of Oxidative Stress

In Vivo Immuno-Spin Trapping: Imaging the Footprints of Oxidative Stress
A plethora of disease processes are associated with elevated reactive species formation and allied reactions with biomolecules that alter cell signaling, induce overt damage, and promote dysfunction of tissues. Unfortunately, effective detection of reactive species in tissues is wrought with issues that significantly limit capacity for validating species identity, establishing accurate concentrations, and identifying anatomic sites of production. These shortcomings reveal the pressing need for new approaches to more precisely assess reactive species generation in vivo. Herein, we describe an in vivo immuno‐spin trapping method for indirectly assessing oxidant levels by detecting free radicals resulting from reaction of oxidants with biomolecules to form stable, immunologically detectable nitrone‐biomolecular adducts. This process couples the reactivity and sensitivity of an electron paramagnetic resonance spin trap with the resolution of confocal imaging to visualize the extent of cell and tissue oxidation and anatomic sites of production by detecting resultant free radical formation. © 2015 by John Wiley & Sons, Inc.
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来源期刊
Current Protocols in Cytometry
Current Protocols in Cytometry Health Professions-Medical Laboratory Technology
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期刊介绍: Published in affiliation with the International Society for Advancement of Cytometry, Current Protocols in Cytometry is a "best practices" collection that distills and organizes the absolute latest techniques from the top cytometry labs and specialists worldwide. It is the most complete set of peer-reviewed protocols for flow and image cytometry available.
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