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Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT
Following a certain type-specific number of mitotic divisions, terminally differentiated cells undergo proliferative senescence, thwarting efforts to expand different cell populations in vitro for the needs of scientific research or medical therapies. The primary cause of this phenomenon is the prog...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160115/ https://www.ncbi.nlm.nih.gov/pubmed/30261016 http://dx.doi.org/10.1371/journal.pone.0204580 |
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author | Petkov, Stoyan Kahland, Tobias Shomroni, Orr Lingner, Thomas Salinas, Gabriela Fuchs, Sigrid Debowski, Katharina Behr, Rüdiger |
author_facet | Petkov, Stoyan Kahland, Tobias Shomroni, Orr Lingner, Thomas Salinas, Gabriela Fuchs, Sigrid Debowski, Katharina Behr, Rüdiger |
author_sort | Petkov, Stoyan |
collection | PubMed |
description | Following a certain type-specific number of mitotic divisions, terminally differentiated cells undergo proliferative senescence, thwarting efforts to expand different cell populations in vitro for the needs of scientific research or medical therapies. The primary cause of this phenomenon is the progressive shortening of the telomeres and the subsequent activation of cell cycle control pathways leading to a block of cell proliferation. Restoration of telomere length by transgenic expression of telomerase reverse transcriptase (TERT) usually results in bypassing of the replicative senescence and ultimately in cell immortalization. To date, there have not been any reports regarding immortalization of cells from common marmoset (Callithrix jacchus), an important non-human primate model for various human diseases, with the use of exogenous human TERT (hTERT). In this study, marmoset fibroblasts were successfully immortalized with transposon-integrated transgenic hTERT and expanded in vitro for over 500 population doublings. Calculation of population doubling levels (PDL) showed that the derived hTERT-transgenic lines had significantly higher proliferation potential than the wild-type fibroblasts, which reached only a maximum of 46 doublings. However, the immortalized cells exhibited differences in the morphology compared with the control fibroblasts and transcriptome analysis also revealed changes in the gene expression patterns. Finally, the karyotypes of all hTERT-transgenic cell lines showed various aberrations such as presence of extra Chromosome 17, isochromosome 21q, or tetraploidy. By single-cell expansion of the least affected monoclonal immortalized line, one sub-clonal line with normal karyotype was established, suggesting the possibility to derive immortal marmoset cells with normal karyotypes. The results of this study are an important step towards the development and optimization of methods for the production of immortalized cells from common marmoset monkeys. |
format | Online Article Text |
id | pubmed-6160115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61601152018-10-19 Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT Petkov, Stoyan Kahland, Tobias Shomroni, Orr Lingner, Thomas Salinas, Gabriela Fuchs, Sigrid Debowski, Katharina Behr, Rüdiger PLoS One Research Article Following a certain type-specific number of mitotic divisions, terminally differentiated cells undergo proliferative senescence, thwarting efforts to expand different cell populations in vitro for the needs of scientific research or medical therapies. The primary cause of this phenomenon is the progressive shortening of the telomeres and the subsequent activation of cell cycle control pathways leading to a block of cell proliferation. Restoration of telomere length by transgenic expression of telomerase reverse transcriptase (TERT) usually results in bypassing of the replicative senescence and ultimately in cell immortalization. To date, there have not been any reports regarding immortalization of cells from common marmoset (Callithrix jacchus), an important non-human primate model for various human diseases, with the use of exogenous human TERT (hTERT). In this study, marmoset fibroblasts were successfully immortalized with transposon-integrated transgenic hTERT and expanded in vitro for over 500 population doublings. Calculation of population doubling levels (PDL) showed that the derived hTERT-transgenic lines had significantly higher proliferation potential than the wild-type fibroblasts, which reached only a maximum of 46 doublings. However, the immortalized cells exhibited differences in the morphology compared with the control fibroblasts and transcriptome analysis also revealed changes in the gene expression patterns. Finally, the karyotypes of all hTERT-transgenic cell lines showed various aberrations such as presence of extra Chromosome 17, isochromosome 21q, or tetraploidy. By single-cell expansion of the least affected monoclonal immortalized line, one sub-clonal line with normal karyotype was established, suggesting the possibility to derive immortal marmoset cells with normal karyotypes. The results of this study are an important step towards the development and optimization of methods for the production of immortalized cells from common marmoset monkeys. Public Library of Science 2018-09-27 /pmc/articles/PMC6160115/ /pubmed/30261016 http://dx.doi.org/10.1371/journal.pone.0204580 Text en © 2018 Petkov et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Petkov, Stoyan Kahland, Tobias Shomroni, Orr Lingner, Thomas Salinas, Gabriela Fuchs, Sigrid Debowski, Katharina Behr, Rüdiger Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT |
title | Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT |
title_full | Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT |
title_fullStr | Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT |
title_full_unstemmed | Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT |
title_short | Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT |
title_sort | immortalization of common marmoset monkey fibroblasts by piggybac transposition of htert |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160115/ https://www.ncbi.nlm.nih.gov/pubmed/30261016 http://dx.doi.org/10.1371/journal.pone.0204580 |
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