In Vitro Evaluation of Cytotoxicity and Oxidative Stress Induced by Multiwalled Carbon Nanotubes in Murine RAW 264.7 Macrophages and Human A549 Lung Cells
Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Methods Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and t...
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Published in | Biomedical and environmental sciences Vol. 24; no. 6; pp. 593 - 601 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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China
Elsevier B.V
01.12.2011
Key Laboratory of Public Health Safety, Ministry of Education, School of Public Health, Fudan University,Shanghai 200032, China%Putuo District Center for Disease Control and Prevention, Shanghai 200333, China%Graduate School of Engineering, Nagoya Institute of Technology, Nagoya 466-8555, Japan%NPFPC Key Laboratory of Contraceptive & Devices, Shanghai Institute of Planned Parenthood Research, Shanghai 200032,China |
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Abstract | Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Methods Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and the MWCNTs suspensions at 2.5, 10, 25, and 100 ug/mL for 24 h. Each treatment was evaluated by cell viability, cytotoxicity and oxidative stress. Results Overall, both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs. DNA salt treatment showed no change compared to the blank control. In both cell lines, significant changes at the doses of 25 and 100 ug/mL treatments were found in cell viabilities, cytotoxicity, and oxidative stress indexes. The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 ug/mL treatment, whereas no change was seen in most of the indexes. The ROS generation in both cell lines went up in minutes, reached the climax within an hour and faded down after several hours. Conclusion Exposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells, that was closely correlated to the increased oxidative stress. |
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AbstractList | OBJECTIVE: To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). METHODS: Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and the MWCNTs suspensions at 2.5, 10, 25, and 100 μg/mL for 24 h. Each treatment was evaluated by cell viability, cytotoxicity and oxidative stress. RESULTS: Overall, both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs. DNA salt treatment showed no change compared to the blank control. In both cell lines, significant changes at the doses of 25 and 100 μg/mL treatments were found in cell viabilities, cytotoxicity, and oxidative stress indexes. The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 μg/mL treatment, whereas no change was seen in most of the indexes. The ROS generation in both cell lines went up in minutes, reached the climax within an hour and faded down after several hours. CONCLUSION: Exposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells, that was closely correlated to the increased oxidative stress. To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and the MWCNTs suspensions at 2.5, 10, 25, and 100 μg/mL for 24 h. Each treatment was evaluated by cell viability, cytotoxicity and oxidative stress. Overall, both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs. DNA salt treatment showed no change compared to the blank control. In both cell lines, significant changes at the doses of 25 and 100 μg/mL treatments were found in cell viabilities, cytotoxicity, and oxidative stress indexes. The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 μg/mL treatment, whereas no change was seen in most of the indexes. The ROS generation in both cell lines went up in minutes, reached the climax within an hour and faded down after several hours. Exposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells, that was closely correlated to the increased oxidative stress. R734.2; Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs).Methods Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type Ⅱ (human A549 lung cells) were exposed to the blank control,DNA salt control,and the MWCNTs suspensions at 2.5,10,25,and 100 μg/mL for 24 h.Each treatment was evaluated by cell viability,cytotoxicity and oxidative stress.Results Overall,both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs.DNA salt treatment showed no change compared to the blank control.In both cell lines,significant changes at the doses of 25 and 100 μg/mL treatments were found in cell viabilities,cytotoxicity,and oxidative stress indexes.The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 μg/mL treatment,whereas no change was seen in most of the indexes.The ROS generation in both cell lines went up in minutes,reached the climax within an hour and faded down after several hours.Conclusion Exposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells,that was closely correlated to the increased oxidative stress. Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Methods Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and the MWCNTs suspensions at 2.5, 10, 25, and 100 ug/mL for 24 h. Each treatment was evaluated by cell viability, cytotoxicity and oxidative stress. Results Overall, both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs. DNA salt treatment showed no change compared to the blank control. In both cell lines, significant changes at the doses of 25 and 100 ug/mL treatments were found in cell viabilities, cytotoxicity, and oxidative stress indexes. The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 ug/mL treatment, whereas no change was seen in most of the indexes. The ROS generation in both cell lines went up in minutes, reached the climax within an hour and faded down after several hours. Conclusion Exposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells, that was closely correlated to the increased oxidative stress. OBJECTIVETo investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs).METHODSCultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and the MWCNTs suspensions at 2.5, 10, 25, and 100 μg/mL for 24 h. Each treatment was evaluated by cell viability, cytotoxicity and oxidative stress.RESULTSOverall, both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs. DNA salt treatment showed no change compared to the blank control. In both cell lines, significant changes at the doses of 25 and 100 μg/mL treatments were found in cell viabilities, cytotoxicity, and oxidative stress indexes. The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 μg/mL treatment, whereas no change was seen in most of the indexes. The ROS generation in both cell lines went up in minutes, reached the climax within an hour and faded down after several hours.CONCLUSIONExposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells, that was closely correlated to the increased oxidative stress. |
Author | CHEN Bo LIU Ying SONG Wei Ming HAYASHI Yasuhiko DING Xun Cheng LI Wei Hua |
AuthorAffiliation | Key Laboratory of Public Health Safety, Ministry of Education, School of Public Health, Fudan University, Shanghai 200032, China Putuo District Center for Disease Control and Prevention, Shanghai 200333, China Graduate School of Engineering, Nagoya Inst#ute of Technology, Nagoya 466-8555, Japan NPFPC Key Laboratory of Contraceptive & Devices, Shanghai Institute of Planned Parenthood Research, Shanghai 200032, China |
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Keywords | Oxidative stress Cytotoxicity A549 cells Multi-wall carbon nanotubes RAW 264.7 cells |
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Notes | Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Methods Cultured macrophages (murine RAW264.7 cells) and alveolar epithelium cells type II (human A549 lung cells) were exposed to the blank control, DNA salt control, and the MWCNTs suspensions at 2.5, 10, 25, and 100 ug/mL for 24 h. Each treatment was evaluated by cell viability, cytotoxicity and oxidative stress. Results Overall, both cell lines had similar patterns in response to the cytotoxicity and oxidative stress of MWCNTs. DNA salt treatment showed no change compared to the blank control. In both cell lines, significant changes at the doses of 25 and 100 ug/mL treatments were found in cell viabilities, cytotoxicity, and oxidative stress indexes. The reactive oxygen species (ROS) generation was also found to be significantly higher at the dose of 10 ug/mL treatment, whereas no change was seen in most of the indexes. The ROS generation in both cell lines went up in minutes, reached the climax within an hour and faded down after several hours. Conclusion Exposure to MWCNTs resulted in a dose-dependent cytotoxicity in cultured RAW264.7 cells and A549 cells, that was closely correlated to the increased oxidative stress. Multi-wall carbon nanotubes; Cytotoxicity; Oxidative stress; RAW 264.7 cells; A549 cells 11-2816/Q http://dx.doi.org/10.3967/0895-3988.2011.06.002 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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Snippet | Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Methods Cultured macrophages... To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). Cultured macrophages (murine RAW264.7... OBJECTIVE: To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs). METHODS: Cultured macrophages... OBJECTIVETo investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs).METHODSCultured macrophages... R734.2; Objective To investigate in vitro cytotoxicity and oxidative stress response induced by multiwalled carbon nanotubes (MWCNTs).Methods Cultured... |
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SubjectTerms | A549 cells A549细胞 Animals Cell Culture Techniques Cell Line Cell Survival - drug effects Cytotoxicity Dose-Response Relationship, Drug Humans Lung - drug effects Lung - enzymology Lung - metabolism Lung - pathology Macrophages, Alveolar - drug effects Macrophages, Alveolar - enzymology Macrophages, Alveolar - metabolism Macrophages, Alveolar - pathology Mice Microscopy, Electron, Scanning Microscopy, Electron, Transmission Microscopy, Fluorescence Multi-wall carbon nanotubes Nanotubes, Carbon - chemistry Nanotubes, Carbon - toxicity Oxidative stress Oxidative Stress - drug effects RAW 264.7 cells Reactive Oxygen Species - metabolism Surface Properties 体外细胞毒性 多壁碳纳米管 小鼠 巨噬细胞 氧化应激反应 肺癌细胞 诱导 |
Title | In Vitro Evaluation of Cytotoxicity and Oxidative Stress Induced by Multiwalled Carbon Nanotubes in Murine RAW 264.7 Macrophages and Human A549 Lung Cells |
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