Cadmium-dependent generation of reactive oxygen species and mitochondrial DNA breaks in photosynthetic and non-photosynthetic strains of Euglena gracilis |
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Authors: | Watanabe Masumi Henmi Kenji Ogawa Ken'ichi Suzuki Tetsuya |
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Affiliation: | 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 |
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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. |
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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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