Selivanov Vitaly A, Zeak Jennifer A, Roca Josep, Cascante Marta, Trucco Massimo, Votyakova Tatyana V
Department of Biochemistry and Molecular Biology, Associated Unit to Consejo Superior de Investigaciones Científicas, Institute of Biomedicine of the University of Barcelona, Barcelona, Spain.
J Biol Chem. 2008 Oct 24;283(43):29292-300. doi: 10.1074/jbc.M801019200. Epub 2008 Aug 7.
Reactive oxygen species (ROS) generation in mitochondria as a side product of electron and proton transport through the inner membrane is important for normal cell operation as well as development of pathology. Matrix and cytosol alkalization stabilizes semiquinone radical, a potential superoxide producer, and we hypothesized that proton deficiency under the excess of electron donors enhances reactive oxygen species generation. We tested this hypothesis by measuring pH dependence of reactive oxygen species released by mitochondria. The experiments were performed in the media with pH varying from 6 to 8 in the presence of complex II substrate succinate or under more physiological conditions with complex I substrates glutamate and malate. Matrix pH was manipulated by inorganic phosphate, nigericine, and low concentrations of uncoupler or valinomycin. We found that high pH strongly increased the rate of free radical generation in all of the conditions studied, even when DeltapH=0 in the presence of nigericin. In the absence of inorganic phosphate, when the matrix was the most alkaline, pH shift in the medium above 7 induced permeability transition accompanied by the decrease of ROS production. ROS production increase induced by the alkalization of medium was observed with intact respiring mitochondria as well as in the presence of complex I inhibitor rotenone, which enhanced reactive oxygen species release. The phenomena revealed in this report are important for understanding mechanisms governing mitochondrial production of reactive oxygen species, in particular that related with uncoupling proteins.
线粒体中作为电子和质子通过内膜运输的副产物而产生的活性氧(ROS),对于正常细胞运作以及病理发展都很重要。线粒体基质和胞质碱化会使半醌自由基(一种潜在的超氧化物产生剂)稳定,我们推测在电子供体过量的情况下质子缺乏会增强活性氧的产生。我们通过测量线粒体释放的活性氧对pH的依赖性来验证这一假设。实验在pH值从6到8变化的介质中进行,介质中存在复合物II底物琥珀酸,或者在更接近生理条件下存在复合物I底物谷氨酸和苹果酸。通过无机磷酸盐、尼日利亚菌素以及低浓度的解偶联剂或缬氨霉素来调控线粒体基质的pH值。我们发现,在所有研究条件下,高pH都会强烈增加自由基产生速率,即使在尼日利亚菌素存在下膜电位差(ΔpH)为0时也是如此。在没有无机磷酸盐的情况下,当线粒体基质碱性最强时,介质pH值高于7会诱导通透性转换,并伴随着活性氧产生的减少。在完整的呼吸线粒体以及存在复合物I抑制剂鱼藤酮(它会增强活性氧释放)的情况下,都观察到了介质碱化诱导的活性氧产生增加。本报告中揭示的这些现象对于理解线粒体活性氧产生的调控机制很重要,特别是与解偶联蛋白相关的机制。