Data · dataset · 2016
In vitro and in vivo genotoxic effects of straight versus tangled multi-walled carbon nanotubes
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Some multi-walled carbon nanotubes (MWCNTs) induce mesothelioma in rodents, straight MWCNTs showing a more pronounced effect than tangled MWCNTs.
Description
As primary and secondary genotoxicity may play a role in MWCNT carcinogenesis, we used a battery of assays for DNA damage and micronuclei to compare the genotoxicity of straight (MWCNT-S) and tangled MWCNTs (MWCNT-T) in vitro (primary genotoxicity) and in vivo (primary or secondary genotoxicity).
C57Bl/6 mice showed a dose-dependent increase in DNA strand breaks, as measured by the comet assay, in lung cells 24 h after a single pharyngeal aspiration of MWCNT-S (1–200 μg/mouse). An increase was also observed for DNA strand breaks in lung and bronchoalveolar lavage (BAL) cells and for micronucleated alveolar type II cells in mice exposed to aerosolized MWCNT-S (8.2–10.8 mg/m 3 ) for 4 d, 4 h/d. No systemic genotoxic effects, assessed by the γ-H2AX assay in blood mononuclear leukocytes or by micronucleated polychromatic erythrocytes (MNPCEs) in bone marrow or blood, were observed for MWCNT-S by either exposure technique.
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MWCNT-T showed a dose-related decrease in DNA damage in BAL and lung cells of mice after a single pharyngeal aspiration (1–200 μg/mouse) and in MNPCEs after inhalation exposure (17.5 mg/m 3 ). In vitro in human bronchial epithelial BEAS-2B cells, MWCNT-S induced DNA strand breaks at low doses (5 and 10 μg/cm 2 ), while MWCNT-T increased strand breakage only at 200 μg/cm 2 . Neither of the MWCNTs was able to induce micronuclei in vitro .
Our findings suggest that both primary and secondary mechanisms may be involved in the genotoxicity of straight MWCNTs.
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- Repository landing page tandf.figshare.com/articles/dataset/_i_In_160_vitro_i_and_i_in_160_vivo_i_genotox… ↗
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- Repository landing page figshare.com/articles/_i_In_160_vitro_i_and_i_in_160_vivo_i_genotoxic_effec… ↗
landing page · from DataCite
- DOI doi.org/10.6084/m9.figshare.1625303 ↗
DOI / persistent id · from DataCite
- DOI doi.org/10.6084/m9.figshare.1625303.v2 ↗
DOI / persistent id · from DataCite
Documentation and papers
- Creative Commons Attribution 4.0 International creativecommons.org/licenses/by/4.0/legalcode ↗
license · from DataCite
- IsSupplementTo 10.3109/17435390.2015.1132345 doi.org/10.3109/17435390.2015.1132345 ↗
publication · from DataCite
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- DataCite API api.datacite.org/dois/10.6084/m9.figshare.1625303.v2 ↗
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- DataCite API api.datacite.org/dois/10.6084/m9.figshare.1625303 ↗
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- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.1625303 ↗
catalogue entry · from DataCite
- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.1625303.v2 ↗
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Topics
- Stated by source
- Biological sciences · Biological sciences · Health sciences · Health sciences · Physical sciences · Physical sciences
- From keywords
- Biochemistry and cell biology · Cancer · Cancer · Medicine & Health · Medicine & Health · Microbiology
Related
Provenance · 2 source records, 18 field assertions
| Source | Key | Last seen | Raw |
|---|---|---|---|
| DataCite | 10.6084/m9.figshare.1625303 | 13 d ago | JSON v1 |
| DataCite | 10.6084/m9.figshare.1625303.v2 | 13 d ago | JSON v1 |
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