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A Mitochondria-Targeted Triphenylphosphonium-Conjugated Nitroxide Functions as a Radioprotector/Mitigator
Jianfei Jiang, Detcho A. Stoyanovsky, Natalia A. Belikova, Yulia Y. Tyurina, Qing Zhao, Muhammad A. Tungekar, Valentyna Kapralova, Zhentai Huang, Arlan H. Mintz, Joel S. Greenberger and Valerian E. Kagan
Vol. 172, No. 6 (Dec., 2009), pp. 706-717
Published by: Radiation Research Society
Stable URL: http://www.jstor.org/stable/27735424
Page Count: 12
You can always find the topics here!Topics: Embryonic cells, Mitochondria, Cardiolipins, Apoptosis, Irradiation, Cytochromes, Superoxides, Incubation, Reactive oxygen species, Endothelial cells
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Removal of excessive mitochondrial reactive oxygen species by electron scavengers and antioxidants is a promising therapeutic strategy to reduce the detrimental effects of radiation exposure. Here we exploited triphenylphosphonium (TPP) cation as a means to target nitroxide radicals to mitochondria. We synthesized a library of TPP-conjugated nitroxides and tested their radioprotective effects in γ-irradiated mouse embryo cells and human epithelial BEAS-2B cells. Cells were incubated with conjugates either before or after irradiation. We found that [2-(1-oxyl-2,2,6,6-tetramethyl-piperidin-4-ylimino)- ethyl]-triphenyl-phosphonium (TPEY-Tempo) significantly blocked radiation-induced apoptosis as revealed by externalization of phosphatidylserine on the cell surface and inhibition of cytochrome c release from mitochondria. Using electron paramagnetic resonance, we showed that TPEY-Tempo was integrated into cells and mitochondria, where it underwent one-electron reduction to hydroxylamine. TPEY-Tempo acted as an electron scavenger that prevented superoxide generation and cardiolipin oxidation in mitochondria. Finally, TPEY-Tempo increased the clonogenic survival rate of irradiated cells. The cellular integration efficiencies of nonradioprotective TPP conjugates, including Mito-Tempo (Alexis, San Diego, CA), were markedly lower, although these homologues were integrated into isolated succinate-energized mitochondria to a similar extent as TPEY-Tempo. We conclude that mitochondrial targeting of TPP-conjugated nitroxides represents a promising approach for the development of novel radioprotectors.
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