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...

Descripción completa

Detalles Bibliográficos
Autores principales: Reimann, Hauke, Stopper, Helga, Hintzsche, Henning
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