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Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line
Mesothelial cells are susceptible to asbestos fiber-induced cytotoxicity and on longer time scales to transformation; the resulting mesothelioma is a highly aggressive neoplasm that is considered as incurable at the present time Zucali et al. (Cancer Treatment Reviews 37:543–558, 2011). Only few mur...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539351/ https://www.ncbi.nlm.nih.gov/pubmed/25877069 http://dx.doi.org/10.1007/s11626-015-9885-z |
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author | Blum, Walter Pecze, László Felley-Bosco, Emanuela Worthmüller-Rodriguez, Janine Wu, Licun Vrugt, Bart de Perrot, Marc Schwaller, Beat |
author_facet | Blum, Walter Pecze, László Felley-Bosco, Emanuela Worthmüller-Rodriguez, Janine Wu, Licun Vrugt, Bart de Perrot, Marc Schwaller, Beat |
author_sort | Blum, Walter |
collection | PubMed |
description | Mesothelial cells are susceptible to asbestos fiber-induced cytotoxicity and on longer time scales to transformation; the resulting mesothelioma is a highly aggressive neoplasm that is considered as incurable at the present time Zucali et al. (Cancer Treatment Reviews 37:543–558, 2011). Only few murine cell culture models of immortalized mesothelial cells and mesothelioma cell lines exist to date. We generated SV40-immortalized cell lines derived from wild-type (WT) and neurofibromatosis 2 (merlin) heterozygote (Nf2+/−) mice, both on a commonly used genetic background, C57Bl/6J. All immortalized mesothelial clones consistently grow in DMEM supplemented with fetal bovine serum. Cells can be passaged for more than 40 times without any signs of morphological changes or a decrease in proliferation rate. The tumor suppressor gene NF2 is one of the most frequently mutated genes in human mesothelioma, but its detailed function is still unknown. Thus, these genotypically distinct cell lines likely relevant for malignant mesothelioma formation are expected to serve as useful in vitro models, in particular to compare with in vivo studies in mice of the same genotype. Furthermore, we generated a novel murine mesothelioma cell line RN5 originating from an Nf2+/− mouse subjected to repeated crocidolite exposure. RN5 cells are highly tumorigenic. |
format | Online Article Text |
id | pubmed-4539351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-45393512015-08-19 Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line Blum, Walter Pecze, László Felley-Bosco, Emanuela Worthmüller-Rodriguez, Janine Wu, Licun Vrugt, Bart de Perrot, Marc Schwaller, Beat In Vitro Cell Dev Biol Anim Article Mesothelial cells are susceptible to asbestos fiber-induced cytotoxicity and on longer time scales to transformation; the resulting mesothelioma is a highly aggressive neoplasm that is considered as incurable at the present time Zucali et al. (Cancer Treatment Reviews 37:543–558, 2011). Only few murine cell culture models of immortalized mesothelial cells and mesothelioma cell lines exist to date. We generated SV40-immortalized cell lines derived from wild-type (WT) and neurofibromatosis 2 (merlin) heterozygote (Nf2+/−) mice, both on a commonly used genetic background, C57Bl/6J. All immortalized mesothelial clones consistently grow in DMEM supplemented with fetal bovine serum. Cells can be passaged for more than 40 times without any signs of morphological changes or a decrease in proliferation rate. The tumor suppressor gene NF2 is one of the most frequently mutated genes in human mesothelioma, but its detailed function is still unknown. Thus, these genotypically distinct cell lines likely relevant for malignant mesothelioma formation are expected to serve as useful in vitro models, in particular to compare with in vivo studies in mice of the same genotype. Furthermore, we generated a novel murine mesothelioma cell line RN5 originating from an Nf2+/− mouse subjected to repeated crocidolite exposure. RN5 cells are highly tumorigenic. Springer US 2015-04-15 2015 /pmc/articles/PMC4539351/ /pubmed/25877069 http://dx.doi.org/10.1007/s11626-015-9885-z Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Article Blum, Walter Pecze, László Felley-Bosco, Emanuela Worthmüller-Rodriguez, Janine Wu, Licun Vrugt, Bart de Perrot, Marc Schwaller, Beat Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
title | Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
title_full | Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
title_fullStr | Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
title_full_unstemmed | Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
title_short | Establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
title_sort | establishment of immortalized murine mesothelial cells and a novel mesothelioma cell line |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539351/ https://www.ncbi.nlm.nih.gov/pubmed/25877069 http://dx.doi.org/10.1007/s11626-015-9885-z |
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