Y Xie1, Z X Zhuang. 1. Department of Toxicology, Chinese Academy of Preventive Medicine, Beijing 100050, China. maze12@163.net
Abstract
OBJECTIVE: To examine whether Reactive Oxygen Species (ROS) is generated, and whether plasma membrane potential and mitochondrial membrane potential are depolarized in Chinese Hamster Lung (CHL) cell lines exposed to Cr (VI). METHODS: CHL cells were incubated with Cr(VI) at 10 mumol/L, 2.5 mumol/L, 0.65 mumol/L for 3 and 6 hours, respectively. The production of ROS was performed by using 2,7-dichlorofluorescin diacetate; The changes in plasma membrane potential were estimated using fluorescent cationic dye DiBAC4; And the changes in mitochondria membrane potential were estimated using fluorescent dye Rhodamine 123. RESULTS: The ROS levels in CHL cells increased in all treated groups compared with the control group (P < 0.01); The plasma membrane potential and mitochondrial membrane potential in CHL cells dissipated after incubated with Cr(VI) at 10 mumol/L for 3 hours and 6 hours (P < 0.01), at 2.5 mumol/L for 6 hours (P < 0.01 or 0.05). CONCLUSION: Cr(VI) causes the dissipation of plasma membrane potential and mitochondrial membrane potential in CHL cell cultures, and Cr(VI)-induced ROS may play a role in the injuries.
OBJECTIVE: To examine whether Reactive Oxygen Species (ROS) is generated, and whether plasma membrane potential and mitochondrial membrane potential are depolarized in Chinese Hamster Lung (CHL) cell lines exposed to Cr (VI). METHODS:CHL cells were incubated with Cr(VI) at 10 mumol/L, 2.5 mumol/L, 0.65 mumol/L for 3 and 6 hours, respectively. The production of ROS was performed by using 2,7-dichlorofluorescin diacetate; The changes in plasma membrane potential were estimated using fluorescent cationic dye DiBAC4; And the changes in mitochondria membrane potential were estimated using fluorescent dye Rhodamine 123. RESULTS: The ROS levels in CHL cells increased in all treated groups compared with the control group (P < 0.01); The plasma membrane potential and mitochondrial membrane potential in CHL cells dissipated after incubated with Cr(VI) at 10 mumol/L for 3 hours and 6 hours (P < 0.01), at 2.5 mumol/L for 6 hours (P < 0.01 or 0.05). CONCLUSION:Cr(VI) causes the dissipation of plasma membrane potential and mitochondrial membrane potential in CHL cell cultures, and Cr(VI)-induced ROS may play a role in the injuries.