University of Antwerp, Belgium.
Free Radic Res. 2010 Jul;44(7):763-72. doi: 10.3109/10715761003782288.
Despite the major impact of ROS on human health, their quantification remains difficult and requires an analytical approach, such as the EPR spin trap technique. In this study, a comparative EPR analysis of different macrophage types stimulated for superoxide and nitric oxide production was performed. U937 monocytes, J774A.1, RAW 264.7 and primary mouse (PMM) macrophages were included. In contrast to the U937 cells, all macrophages produced significant EPR signals after stimulation. The use of PMA as stimulator and CM-H as spin probe led to the highest response in EPR signals for detection of O(2)(.-) as nitroxide radical. A combination of LPS and IFN-gamma and the spin trap [Fe(DETC)(2)] turned out to be the best combination for the production and detection of intracellular NO spin adducts. In conclusion, this study established practical experimental conditions for the EPR analysis of O(2)(.-) and NO produced by different types of activated macrophages.
尽管活性氧 (ROS) 对人类健康有重大影响,但它们的定量仍然很困难,需要采用分析方法,如电子顺磁共振 (EPR) 自旋捕获技术。本研究对不同类型的巨噬细胞进行了 EPR 分析,以研究其在超氧和一氧化氮产生方面的作用。实验选用了 U937 单核细胞、J774A.1、RAW 264.7 和原代小鼠 (PMM) 巨噬细胞。与 U937 细胞不同,所有巨噬细胞在刺激后均产生了显著的 EPR 信号。使用 PMA 作为刺激物和 CM-H 作为自旋探针可检测到最高的 O(2)(.-)作为氮氧自由基的 EPR 信号。LPS 和 IFN-γ与[Fe(DETC)(2)]的组合是产生和检测细胞内 NO 自旋加合物的最佳组合。总之,本研究建立了 EPR 分析不同类型激活巨噬细胞产生的 O(2)(.-)和 NO 的实用实验条件。