Cargando…
Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells
Micronuclei are small nuclear cellular structures containing whole chromosomes or chromosomal fragments. While there is a lot of information available about the origin and formation of micronuclei, less is known about the fate of micronuclei and micronucleated cells. Possible fates include extrusion...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502055/ https://www.ncbi.nlm.nih.gov/pubmed/32681187 http://dx.doi.org/10.1007/s00204-020-02840-0 |
_version_ | 1783584150781952000 |
---|---|
author | Reimann, Hauke Stopper, Helga Hintzsche, Henning |
author_facet | Reimann, Hauke Stopper, Helga Hintzsche, Henning |
author_sort | Reimann, Hauke |
collection | PubMed |
description | Micronuclei are small nuclear cellular structures containing whole chromosomes or chromosomal fragments. While there is a lot of information available about the origin and formation of micronuclei, less is known about the fate of micronuclei and micronucleated cells. Possible fates include extrusion, degradation, reincorporation and persistence. Live cell imaging was performed to quantitatively analyse the fates of micronuclei and micronucleated cells occurring in vitro. Imaging was conducted for up to 96 h in HeLa-H2B-GFP cells treated with 0.5, 1 and 2 µg/ml etoposide. While a minority of micronuclei was reincorporated into the main nucleus during mitosis, the majority of micronuclei persisted without any alterations. Degradation and extrusion were observed rarely or never. The presence of micronuclei affected the proliferation of the daughter cells and also had an influence on cell death rates. Mitotic errors were found to be clearly increased in micronucleus-containing cells. The results show that micronuclei and micronucleated cells can, although delayed in cell cycle, sustain for multiple divisions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00204-020-02840-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7502055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75020552020-10-01 Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells Reimann, Hauke Stopper, Helga Hintzsche, Henning Arch Toxicol Genotoxicity and Carcinogenicity Micronuclei are small nuclear cellular structures containing whole chromosomes or chromosomal fragments. While there is a lot of information available about the origin and formation of micronuclei, less is known about the fate of micronuclei and micronucleated cells. Possible fates include extrusion, degradation, reincorporation and persistence. Live cell imaging was performed to quantitatively analyse the fates of micronuclei and micronucleated cells occurring in vitro. Imaging was conducted for up to 96 h in HeLa-H2B-GFP cells treated with 0.5, 1 and 2 µg/ml etoposide. While a minority of micronuclei was reincorporated into the main nucleus during mitosis, the majority of micronuclei persisted without any alterations. Degradation and extrusion were observed rarely or never. The presence of micronuclei affected the proliferation of the daughter cells and also had an influence on cell death rates. Mitotic errors were found to be clearly increased in micronucleus-containing cells. The results show that micronuclei and micronucleated cells can, although delayed in cell cycle, sustain for multiple divisions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00204-020-02840-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-07-17 2020 /pmc/articles/PMC7502055/ /pubmed/32681187 http://dx.doi.org/10.1007/s00204-020-02840-0 Text en © The Author(s) 2020 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/. |
spellingShingle | Genotoxicity and Carcinogenicity Reimann, Hauke Stopper, Helga Hintzsche, Henning Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells |
title | Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells |
title_full | Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells |
title_fullStr | Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells |
title_full_unstemmed | Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells |
title_short | Long-term fate of etoposide-induced micronuclei and micronucleated cells in Hela-H2B-GFP cells |
title_sort | long-term fate of etoposide-induced micronuclei and micronucleated cells in hela-h2b-gfp cells |
topic | Genotoxicity and Carcinogenicity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502055/ https://www.ncbi.nlm.nih.gov/pubmed/32681187 http://dx.doi.org/10.1007/s00204-020-02840-0 |
work_keys_str_mv | AT reimannhauke longtermfateofetoposideinducedmicronucleiandmicronucleatedcellsinhelah2bgfpcells AT stopperhelga longtermfateofetoposideinducedmicronucleiandmicronucleatedcellsinhelah2bgfpcells AT hintzschehenning longtermfateofetoposideinducedmicronucleiandmicronucleatedcellsinhelah2bgfpcells |