Armeni Tatiana, Cianfruglia Laura, Piva Francesco, Urbanelli Lorena, Luisa Caniglia Maria, Pugnaloni Armanda, Principato Giovanni
Department of Clinical Sciences, Section of Biochemistry, Biology, and Physics, Università Politecnica delle Marche, Ancona, Italy.
Department of Clinical Sciences, Section of Biochemistry, Biology, and Physics, Università Politecnica delle Marche, Ancona, Italy.
Free Radic Biol Med. 2014 Feb;67:451-9. doi: 10.1016/j.freeradbiomed.2013.12.005. Epub 2013 Dec 12.
The mitochondrial pool of GSH (glutathione) is considered the major redox system in maintaining matrix redox homeostasis, preserving sulfhydryl groups of mitochondrial proteins in appropriate redox state, in defending mitochondrial DNA integrity and protecting mitochondrial-derived ROS, and in defending mitochondrial membranes against oxidative damage. Despite its importance in maintaining mitochondrial functionality, GSH is synthesized exclusively in the cytoplasm and must be actively transported into mitochondria. In this work we found that SLG (S-D-lactoylglutathione), an intermediate of the glyoxalase system, can enter the mitochondria and there be hydrolyzed from mitochondrial glyoxalase II enzyme to D-lactate and GSH. To demonstrate SLG transport from cytosol to mitochondria we used radiolabeled compounds and the results showed two different kinetic curves for SLG or GSH substrates, indicating different kinetic transport. Also, the incubation of functionally and intact mitochondria with SLG showed increased GSH levels in normal mitochondria and in artificially uncoupled mitochondria, demonstrating transport not linked to ATP presence. As well mitochondrial-swelling assay confirmed SLG entrance into organelles. Moreover we observed oxygen uptake and generation of membrane potential probably linked to D-lactate oxidation which is a product of SLG hydrolysis. The latter data were confirmed by oxidation of D-lactate in mitochondria evaluated by measuring mitochondrial D-lactate dehydrogenize activity. In this work we also showed the presence of mitochondrial glyoxalase II in inter-membrane space and mitochondrial matrix and we investigated the role of SLG in whole cells. In conclusion, this work showed new alternative sources of GSH supply to the mitochondria by SLG, an intermediate of the glyoxalase system.
谷胱甘肽(GSH)的线粒体池被认为是维持基质氧化还原稳态、使线粒体蛋白质的巯基保持在适当氧化还原状态、保护线粒体DNA完整性和保护线粒体衍生的活性氧以及保护线粒体膜免受氧化损伤的主要氧化还原系统。尽管其在维持线粒体功能方面很重要,但GSH仅在细胞质中合成,必须被主动转运到线粒体中。在这项工作中,我们发现乙二醛酶系统的中间体S-D-乳酰谷胱甘肽(SLG)可以进入线粒体,并在那里被线粒体乙二醛酶II水解为D-乳酸和GSH。为了证明SLG从细胞质转运到线粒体,我们使用了放射性标记化合物,结果显示SLG或GSH底物有两条不同的动力学曲线,表明存在不同动力的转运。此外,用SLG孵育功能完整的线粒体表明,正常线粒体和人工解偶联的线粒体中GSH水平都有所增加,这表明转运与ATP的存在无关。线粒体肿胀试验也证实了SLG进入细胞器。此外,我们观察到氧气摄取和膜电位的产生可能与D-乳酸氧化有关,D-乳酸是SLG水解的产物。通过测量线粒体D-乳酸脱氢酶活性评估线粒体中D-乳酸的氧化,证实了后者的数据。在这项工作中,我们还显示了线粒体外膜间隙和线粒体基质中存在线粒体乙二醛酶II,并研究了SLG在全细胞中的作用。总之,这项工作表明乙二醛酶系统的中间体SLG为线粒体提供GSH的新的替代来源。