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Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells

Growth arrested Swiss mouse embryonic 3T3 cells are used as feeders to support the growth of epidermal keratinocytes and several other target cells. The 3T3 cells have been extensively subcultured owing to their popularity and wide distribution in the world and, as a consequence selective inclusion...

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Autores principales: Chugh, Rishi Man, Chaturvedi, Madhusudan, Yerneni, Lakshmana Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370869/
https://www.ncbi.nlm.nih.gov/pubmed/25799110
http://dx.doi.org/10.1371/journal.pone.0122056
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author Chugh, Rishi Man
Chaturvedi, Madhusudan
Yerneni, Lakshmana Kumar
author_facet Chugh, Rishi Man
Chaturvedi, Madhusudan
Yerneni, Lakshmana Kumar
author_sort Chugh, Rishi Man
collection PubMed
description Growth arrested Swiss mouse embryonic 3T3 cells are used as feeders to support the growth of epidermal keratinocytes and several other target cells. The 3T3 cells have been extensively subcultured owing to their popularity and wide distribution in the world and, as a consequence selective inclusion of variants is a strong possibility in them. Inadvertently selected variants expressing innate resistance to mitomycin C may continue to proliferate even after treatment with such growth arresting agents. The failure of growth arrest can lead to a serious risk of proliferative feeder contamination in target cell cultures. In this study, we passaged Swiss 3T3 cells (CCL-92, ATCC) by different seeding densities and incubation periods. We tested the resultant cultures for differences in anchorage-independent growth, resumption of proliferation after mitomycin C treatment and occurrence of proliferative feeder contaminants in an epidermal keratinocyte co-culture system. The study revealed subculture dependent differential responses. The cultures of a particular subculture procedure displayed unique cell size distribution and disintegrated completely in 6 weeks following mitomycin C treatment, but their repeated subculture resulted in feeder regrowth as late as 11 weeks after the growth arrest. In contrast, mitomycin C failed to inhibit cell proliferation in cultures of the other subculture schemes and also in a clone that was established from a transformation focus of super-confluent culture. The resultant proliferative feeder cells contaminated the keratinocyte cultures. The anchorage-independent growth appeared in late passages as compared with the expression of mitomycin C resistance in earlier passages. The feeder regrowth was prevented by identifying a safe subculture protocol that discouraged the inclusion of resistant variants. We advocate routine anchorage-independent growth assay and absolute confirmation of feeder disintegration to qualify feeder batches and caution on the use of fetal bovine serum.
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spelling pubmed-43708692015-04-04 Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells Chugh, Rishi Man Chaturvedi, Madhusudan Yerneni, Lakshmana Kumar PLoS One Research Article Growth arrested Swiss mouse embryonic 3T3 cells are used as feeders to support the growth of epidermal keratinocytes and several other target cells. The 3T3 cells have been extensively subcultured owing to their popularity and wide distribution in the world and, as a consequence selective inclusion of variants is a strong possibility in them. Inadvertently selected variants expressing innate resistance to mitomycin C may continue to proliferate even after treatment with such growth arresting agents. The failure of growth arrest can lead to a serious risk of proliferative feeder contamination in target cell cultures. In this study, we passaged Swiss 3T3 cells (CCL-92, ATCC) by different seeding densities and incubation periods. We tested the resultant cultures for differences in anchorage-independent growth, resumption of proliferation after mitomycin C treatment and occurrence of proliferative feeder contaminants in an epidermal keratinocyte co-culture system. The study revealed subculture dependent differential responses. The cultures of a particular subculture procedure displayed unique cell size distribution and disintegrated completely in 6 weeks following mitomycin C treatment, but their repeated subculture resulted in feeder regrowth as late as 11 weeks after the growth arrest. In contrast, mitomycin C failed to inhibit cell proliferation in cultures of the other subculture schemes and also in a clone that was established from a transformation focus of super-confluent culture. The resultant proliferative feeder cells contaminated the keratinocyte cultures. The anchorage-independent growth appeared in late passages as compared with the expression of mitomycin C resistance in earlier passages. The feeder regrowth was prevented by identifying a safe subculture protocol that discouraged the inclusion of resistant variants. We advocate routine anchorage-independent growth assay and absolute confirmation of feeder disintegration to qualify feeder batches and caution on the use of fetal bovine serum. Public Library of Science 2015-03-23 /pmc/articles/PMC4370869/ /pubmed/25799110 http://dx.doi.org/10.1371/journal.pone.0122056 Text en © 2015 Chugh 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chugh, Rishi Man
Chaturvedi, Madhusudan
Yerneni, Lakshmana Kumar
Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells
title Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells
title_full Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells
title_fullStr Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells
title_full_unstemmed Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells
title_short Occurrence and Control of Sporadic Proliferation in Growth Arrested Swiss 3T3 Feeder Cells
title_sort occurrence and control of sporadic proliferation in growth arrested swiss 3t3 feeder cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370869/
https://www.ncbi.nlm.nih.gov/pubmed/25799110
http://dx.doi.org/10.1371/journal.pone.0122056
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