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 inBiomedical and environmental sciences Vol. 24; no. 6; pp. 593 - 601
Main Authors CHEN, Bo, LIU, Ying, SONG, Wei Ming, HAYASHI, Yasuhiko, DING, Xun Cheng, LI, Wei Hua
Format Journal Article
LanguageEnglish
Published 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.
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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Copyright 2011 The Editorial Board of Biomedical and Environmental Sciences
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Keywords Oxidative stress
Cytotoxicity
A549 cells
Multi-wall carbon nanotubes
RAW 264.7 cells
Language English
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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
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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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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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https://dx.doi.org/10.3967/0895-3988.2011.06.002
https://www.ncbi.nlm.nih.gov/pubmed/22365394
https://search.proquest.com/docview/923954398
https://d.wanfangdata.com.cn/periodical/bes201106002
Volume 24
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