A comparison of acute and long-term effects of industrial multiwalled carbon nanotubes on human lung and immune cells in vitro
0301 basic medicine
Micronucleus Tests
Cell Death
Dose-Response Relationship, Drug
Cell Survival
Nanotubes, Carbon
T-Lymphocytes
Tetrazolium Salts
Apoptosis
Asbestos
Epithelial Cells
Immunohistochemistry
Endocytosis
Jurkat Cells
Thiazoles
03 medical and health sciences
Microscopy, Electron, Transmission
Humans
Comet Assay
Reactive Oxygen Species
Lung
Cell Proliferation
DOI:
10.1016/j.toxlet.2010.11.012
Publication Date:
2010-11-27T09:40:23Z
AUTHORS (10)
ABSTRACT
The close resemblance of carbon nanotubes to asbestos fibers regarding their high aspect ratio, biopersistence and reactivity increases public concerns on the widespread use of these materials. The purpose of this study was not only to address the acute adverse effects of industrially produced multiwalled carbon nanotubes (MWCNTs) on human lung and immune cells in vitro but also to further understand if their accumulation and biopersistence leads to long-term consequences or induces adaptive changes in these cells. In contrast to asbestos fibers, pristine MWCNTs did not induce overt cell death in A549 lung epithelial cells and Jurkat T lymphocytes after acute exposure to high doses of this material (up to 30 μg/ml). Nevertheless, very high levels of reactive oxygen species (ROS) and decreased metabolic activity were observed which might affect long-term viability of these cells. However, the continuous presence of low amounts of MWCNTs (0.5 μg/ml) for 6 months did not have major adverse long-term effects although large amounts of nanotubes accumulated at least in A549 cells. Moreover, MWCNTs did not appear to induce adaptive mechanisms against particle stress in long-term treated A549 cells. Our study demonstrates that despite the high potential for ROS formation, pristine MWCNTs can accumulate and persist within cells without having major long-term consequences or inducing adaptive mechanisms.
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