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Cadmium-dependent generation of reactive oxygen species and mitochondrial DNA breaks in photosynthetic and non-photosynthetic strains of Euglena gracilis
Authors:Watanabe Masumi  Henmi Kenji  Ogawa Ken'ichi  Suzuki Tetsuya
Institution:Division of Life Sciences, Graduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato, Hakodate, Hokkaido 041-8611, Japan. m-wata@fish.hokudai.ac.jp
Abstract:The photosynthetic strain Z of Euglena gracilis is more susceptible to cadmium chloride (Cd) than the non-photosynthetic strain SMZ. We investigated the correlation of intracellular reactive oxygen species (ROS) levels with Cd-induced cellular damage. Flow cytometry with dihydrorhodamine 123 showed that strain Z generated higher levels of ROS, probably H(2)O(2) and/or ONOO(-), than strain SMZ, and that this difference between the two strains became more pronounced with increasing Cd dose. The levels of ROS increased at cytotoxic concentrations of Cd, at over 10 microM Cd for Z and 50 microM Cd for SMZ. These results show an association of Cd cytotoxicity with ROS generation. Considering that strain SMZ is non-photosynthetic, the higher levels of ROS in strain Z might be due to blockage of photosynthetic electron flow by Cd. Using terminal deoxyribonucleotidyl transferase-mediated dUTP nick end-labeling analysis in combination with 4',6-diamidino-2-phenylindole, dihydrochloride staining, we observed DNA breaks in the mitochondria of both strains after Cd exposure. The results suggest that the mitochondrion is the primary target organelle of Cd in E. gracilis cells.
Keywords:Cadmium  Cytotoxicity  DNA strand breaks  Flow cytometry  Mitochondria  Oxidative stress  Reactive oxygen species  DAPI  4′  6-diamidino-2-phenylindole  dihydrochloride  DHR  dihydrorhodamine 123  DMSO  dimethyl sulfoxide  EDTA  ethylenediamine tetraacetic acid  HFLUOR  dihydrofluorescein  KH  Koren–Hutner  8-OHdG  8-hydroxy-2′-deoxyguanosine  PBS (?)  Ca/Mg-free phosphate-buffered saline  ROS  reactive oxygen species  TUNEL  terminal deoxyribonucleotidyl transferase-mediated dUTP nick end-labeling  
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