In vitro evaluation of cytotoxicity and oxidative stress induced by multiwalled carbon nanotubes in murine RAW 264.7 macrophages and human A549 lung cells.
- Author:
Bo CHEN
1
;
Ying LIU
;
Wei Ming SONG
;
Yasuhiko HAYASHI
;
Xun Cheng DING
;
Wei Hua LI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cell Culture Techniques; Cell Line; Cell Survival; drug effects; Dose-Response Relationship, Drug; Humans; Lung; drug effects; enzymology; metabolism; pathology; Macrophages, Alveolar; drug effects; enzymology; metabolism; pathology; Mice; Microscopy, Electron, Scanning; Microscopy, Electron, Transmission; Microscopy, Fluorescence; Nanotubes, Carbon; chemistry; toxicity; Oxidative Stress; drug effects; Reactive Oxygen Species; metabolism; Surface Properties
- From: Biomedical and Environmental Sciences 2011;24(6):593-601
- CountryChina
- Language:English
-
Abstract:
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.
