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In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture
BACKGROUND: Multiwalled carbon nanotubes (MWCNTs) are suspected lung carcinogens because their shape and size are similar to asbestos. Various MWCNT types are manufactured; however, only MWNT-7 is classified into Group 2B by The International Agency for Research on Cancer. MWNT-7’s carcinogenicity i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580184/ https://www.ncbi.nlm.nih.gov/pubmed/36258253 http://dx.doi.org/10.1186/s41021-022-00253-2 |
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author | Horibata, Katsuyoshi Takasawa, Hironao Hojo, Motoki Taquahashi, Yuhji Shigano, Miyuki Yokota, Satoshi Kobayashi, Norihiro Sugiyama, Kei-ichi Honma, Masamitsu Hamada, Shuichi |
author_facet | Horibata, Katsuyoshi Takasawa, Hironao Hojo, Motoki Taquahashi, Yuhji Shigano, Miyuki Yokota, Satoshi Kobayashi, Norihiro Sugiyama, Kei-ichi Honma, Masamitsu Hamada, Shuichi |
author_sort | Horibata, Katsuyoshi |
collection | PubMed |
description | BACKGROUND: Multiwalled carbon nanotubes (MWCNTs) are suspected lung carcinogens because their shape and size are similar to asbestos. Various MWCNT types are manufactured; however, only MWNT-7 is classified into Group 2B by The International Agency for Research on Cancer. MWNT-7’s carcinogenicity is strongly related to inflammatory reactions. On the other hand, inconsistent results on MWNT-7 genotoxicity have been reported. We previously observed no significant differences in both Pig-a (blood) and gpt (lung) mutant frequencies between MWNT-7-intratracheally treated and negative control rats. In this study, to investigate in vivo MWNT-7 genotoxicity on various endpoints, we attempted to develop a lung micronucleus assay through ex vivo culture targeting the cellular fraction of Clara cells and alveolar Type II (AT-II) cells, known as the initiating cells of lung cancer. Using this system, we analyzed the in vivo MWNT-7 genotoxicity induced by both whole-body inhalation exposure and intratracheal instillation. We also conducted an erythrocyte micronucleus assay using the samples obtained from animals under intratracheal instillation to investigate the tissue specificity of MWNT-7 induced genotoxicities. RESULTS: We detected a significant increase in the incidence of micronucleated cells derived from the cellular fraction of Clara cells and AT-II cells in both MWNT-7-treated and positive control groups compared to the negative control group under both whole-body inhalation exposures and intratracheal instillation. Additionally, the erythrocyte micronucleus assay detected a significant increase in the incidence of micronucleated reticulocytes only in the positive control group. CONCLUSIONS: Our findings indicated that MWNT-7 was genotoxic in the lungs directly exposed by both the body inhalation and intratracheal instillation but not in the hematopoietic tissue. |
format | Online Article Text |
id | pubmed-9580184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95801842022-10-20 In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture Horibata, Katsuyoshi Takasawa, Hironao Hojo, Motoki Taquahashi, Yuhji Shigano, Miyuki Yokota, Satoshi Kobayashi, Norihiro Sugiyama, Kei-ichi Honma, Masamitsu Hamada, Shuichi Genes Environ Short Report BACKGROUND: Multiwalled carbon nanotubes (MWCNTs) are suspected lung carcinogens because their shape and size are similar to asbestos. Various MWCNT types are manufactured; however, only MWNT-7 is classified into Group 2B by The International Agency for Research on Cancer. MWNT-7’s carcinogenicity is strongly related to inflammatory reactions. On the other hand, inconsistent results on MWNT-7 genotoxicity have been reported. We previously observed no significant differences in both Pig-a (blood) and gpt (lung) mutant frequencies between MWNT-7-intratracheally treated and negative control rats. In this study, to investigate in vivo MWNT-7 genotoxicity on various endpoints, we attempted to develop a lung micronucleus assay through ex vivo culture targeting the cellular fraction of Clara cells and alveolar Type II (AT-II) cells, known as the initiating cells of lung cancer. Using this system, we analyzed the in vivo MWNT-7 genotoxicity induced by both whole-body inhalation exposure and intratracheal instillation. We also conducted an erythrocyte micronucleus assay using the samples obtained from animals under intratracheal instillation to investigate the tissue specificity of MWNT-7 induced genotoxicities. RESULTS: We detected a significant increase in the incidence of micronucleated cells derived from the cellular fraction of Clara cells and AT-II cells in both MWNT-7-treated and positive control groups compared to the negative control group under both whole-body inhalation exposures and intratracheal instillation. Additionally, the erythrocyte micronucleus assay detected a significant increase in the incidence of micronucleated reticulocytes only in the positive control group. CONCLUSIONS: Our findings indicated that MWNT-7 was genotoxic in the lungs directly exposed by both the body inhalation and intratracheal instillation but not in the hematopoietic tissue. BioMed Central 2022-10-19 /pmc/articles/PMC9580184/ /pubmed/36258253 http://dx.doi.org/10.1186/s41021-022-00253-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Short Report Horibata, Katsuyoshi Takasawa, Hironao Hojo, Motoki Taquahashi, Yuhji Shigano, Miyuki Yokota, Satoshi Kobayashi, Norihiro Sugiyama, Kei-ichi Honma, Masamitsu Hamada, Shuichi In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
title | In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
title_full | In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
title_fullStr | In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
title_full_unstemmed | In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
title_short | In vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
title_sort | in vivo genotoxicity assessment of a multiwalled carbon nanotube in a mouse ex vivo culture |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580184/ https://www.ncbi.nlm.nih.gov/pubmed/36258253 http://dx.doi.org/10.1186/s41021-022-00253-2 |
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