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Multiwall carbon nano‐onions induce DNA damage and apoptosis in human umbilical vein endothelial cells
Authors:Yuying Xu  Shuang‐Ying Wang  Jie Yang  Xiaomin Gu  Jun Zhang  Yi‐Fan Zheng  Jun Yang  Lihong Xu  Xin‐Qiang Zhu
Affiliation:1. Department of Toxicology, Zhejiang University School of Public Health, , Hangzhou, Zhejiang 310058, China;2. Department of Biochemistry and Genetics, Zhejiang University School of Medicine, , Hangzhou, Zhejiang 310058, China;3. Shangcheng Center for Disease Control and Prevention, , Hangzhou, Zhejiang 310009, China;4. Department of Toxicology, Hangzhou Normal University School of Public Health, , Hangzhou, Zhejiang 310036, China
Abstract:Growing evidence has indicated the potential adverse effects on cardiovascular system of some nanomaterials, including fullerenes. In this study, we have evaluated the biological effects of multiwall carbon nano‐onions (MWCNOs) (average size of 31.2 nm, ζ potential of 1.6 mV) on human umbilical vein endothelial cells (HUVECs). It was found that MWCNOs exhibited a dose‐dependent inhibitory effect on cell growth; EC50 was 44.12 μg/mL. Thus, three concentrations were chosen (0.2, 1, and 5 μg/mL) for further experiments. Flow cytometry analysis revealed that 1 and 5 μg/mL MWCNOs could induce apoptosis in HUVECs, the apoptotic rates were 12% and 24% at 24 h after exposure. On the other hand, MWCNOs did not affect the cell cycle distribution during 24 h period. Using γH2AX foci formation as an indicator for DNA damage, it was shown that 5 μg/mL MWCNOs can induce γH2AX foci formation in HUVECs at 6, 12, and 24 h after treatment, whereas 0.2 μg/mL MWCNOs induced γH2AX foci formation only at 6 h after treatment. In addition, all three concentrations of MWCNOs induced the generation of reactive oxygen species (ROS), and inhibition of ROS generation can partially decrease the γH2AX foci formation induced by MWCNOs. Taken together, these data first suggested that MWCNOs can induce DNA damage and apoptosis in HUVECs, and that ROS might be involved in this process. © 2011 Wiley Periodicals, Inc. Environ Toxicol 28: 442–450, 2013.
Keywords:apoptosis  cell cycle  reactive oxygen species
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