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Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells
Exposure to asbestos fibers increases the risk of mesothelioma in humans. One hypothetical carcinogenic mechanism is that asbestos fibers may directly induce mutations in mesothelial cells. Although the uptake of asbestos fibers by mesothelial cells is recognized, methods for the quantification of t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705149/ https://www.ncbi.nlm.nih.gov/pubmed/23874067 http://dx.doi.org/10.3164/jcbn.12-104 |
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author | Yamashita, Kyoko Nagai, Hirotaka Kondo, Yuji Misawa, Nobuaki Toyokuni, Shinya |
author_facet | Yamashita, Kyoko Nagai, Hirotaka Kondo, Yuji Misawa, Nobuaki Toyokuni, Shinya |
author_sort | Yamashita, Kyoko |
collection | PubMed |
description | Exposure to asbestos fibers increases the risk of mesothelioma in humans. One hypothetical carcinogenic mechanism is that asbestos fibers may directly induce mutations in mesothelial cells. Although the uptake of asbestos fibers by mesothelial cells is recognized, methods for the quantification of the uptake have not been well established. In the present study, we evaluated two distinct methods, using crocidolite fibers and MeT5A mesothelial cells. One method is histological evaluation using the cell-block technique, which allows for the direct cross-sectional observation of cells and fibers. We found the bright field observation with ×1000 magnification (oil-immersion) of the sample with Kernechtrot staining was most suitable for this purpose. The other method is flow cytometric analysis, which permits the evaluation of a much larger number of cells. We observed that the side scatter (SSC) increased with the intracellular fibers, and that the “mean SSC ratio (treated/control)” was useful for quantification. We could collect the cells with abundant internalized crocidolite fibers by sorting. Results of the two methodologies were correlated well in the experiments. The quantities of internalized fibers increased with incubation time and loaded dosage, but they were inversely associated with cellular density in culture. |
format | Online Article Text |
id | pubmed-3705149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-37051492013-07-19 Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells Yamashita, Kyoko Nagai, Hirotaka Kondo, Yuji Misawa, Nobuaki Toyokuni, Shinya J Clin Biochem Nutr Original Article Exposure to asbestos fibers increases the risk of mesothelioma in humans. One hypothetical carcinogenic mechanism is that asbestos fibers may directly induce mutations in mesothelial cells. Although the uptake of asbestos fibers by mesothelial cells is recognized, methods for the quantification of the uptake have not been well established. In the present study, we evaluated two distinct methods, using crocidolite fibers and MeT5A mesothelial cells. One method is histological evaluation using the cell-block technique, which allows for the direct cross-sectional observation of cells and fibers. We found the bright field observation with ×1000 magnification (oil-immersion) of the sample with Kernechtrot staining was most suitable for this purpose. The other method is flow cytometric analysis, which permits the evaluation of a much larger number of cells. We observed that the side scatter (SSC) increased with the intracellular fibers, and that the “mean SSC ratio (treated/control)” was useful for quantification. We could collect the cells with abundant internalized crocidolite fibers by sorting. Results of the two methodologies were correlated well in the experiments. The quantities of internalized fibers increased with incubation time and loaded dosage, but they were inversely associated with cellular density in culture. the Society for Free Radical Research Japan 2013-07 2013-06-01 /pmc/articles/PMC3705149/ /pubmed/23874067 http://dx.doi.org/10.3164/jcbn.12-104 Text en Copyright © 2013 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yamashita, Kyoko Nagai, Hirotaka Kondo, Yuji Misawa, Nobuaki Toyokuni, Shinya Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
title | Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
title_full | Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
title_fullStr | Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
title_full_unstemmed | Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
title_short | Evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
title_sort | evaluation of two distinct methods to quantify the uptake of crocidolite fibers by mesothelial cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705149/ https://www.ncbi.nlm.nih.gov/pubmed/23874067 http://dx.doi.org/10.3164/jcbn.12-104 |
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