Seo Byoung Boo, Marella Mathieu, Yagi Takao, Matsuno-Yagi Akemi
Division of Biochemistry, Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
FEBS Lett. 2006 Nov 13;580(26):6105-8. doi: 10.1016/j.febslet.2006.10.008. Epub 2006 Oct 16.
Using rat dopaminergic and human neuroblastoma cell lines transduced with the NDI1 gene encoding the internal NADH dehydrogenase (Ndi1) from Saccharomyces cerevisiae, we investigated reactive oxygen species (ROS) generation caused by complex I inhibition. Incubation of non-transduced cells with rotenone elicited oxidative damage to mitochondrial DNA as well as lipid peroxidation. In contrast, oxidative stress was significantly decreased when the cells were transduced with NDI1. Furthermore, mitochondria from the NDI1-transduced cells showed a suppressed rate of ROS formation by the complex I inhibitors. We conclude that the Ndi1 enzyme is able to suppress ROS overproduction from defective complex I.
我们使用转导了编码来自酿酒酵母的内部NADH脱氢酶(Ndi1)的NDI1基因的大鼠多巴胺能细胞系和人神经母细胞瘤细胞系,研究了由复合体I抑制引起的活性氧(ROS)生成。用鱼藤酮孵育未转导的细胞会引发线粒体DNA的氧化损伤以及脂质过氧化。相比之下,当细胞转导NDI1时,氧化应激显著降低。此外,来自转导NDI1的细胞的线粒体显示出复合体I抑制剂抑制ROS形成的速率。我们得出结论,Ndi1酶能够抑制有缺陷的复合体I产生的ROS过量生成。