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Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano

Adult stem cells are proposed to have acquired special features to prevent an accumulation of DNA-replication errors. Two such mechanisms, frequently suggested to serve this goal are cellular quiescence, and non-random segregation of DNA strands during stem cell division, a theory designated as the...

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Autores principales: Verdoodt, Freija, Willems, Maxime, Mouton, Stijn, De Mulder, Katrien, Bert, Wim, Houthoofd, Wouter, Smith, Julian, Ladurner, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261893/
https://www.ncbi.nlm.nih.gov/pubmed/22276162
http://dx.doi.org/10.1371/journal.pone.0030227
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author Verdoodt, Freija
Willems, Maxime
Mouton, Stijn
De Mulder, Katrien
Bert, Wim
Houthoofd, Wouter
Smith, Julian
Ladurner, Peter
author_facet Verdoodt, Freija
Willems, Maxime
Mouton, Stijn
De Mulder, Katrien
Bert, Wim
Houthoofd, Wouter
Smith, Julian
Ladurner, Peter
author_sort Verdoodt, Freija
collection PubMed
description Adult stem cells are proposed to have acquired special features to prevent an accumulation of DNA-replication errors. Two such mechanisms, frequently suggested to serve this goal are cellular quiescence, and non-random segregation of DNA strands during stem cell division, a theory designated as the immortal strand hypothesis. To date, it has been difficult to test the in vivo relevance of both mechanisms in stem cell systems. It has been shown that in the flatworm Macrostomum lignano pluripotent stem cells (neoblasts) are present in adult animals. We sought to address by which means M. lignano neoblasts protect themselves against the accumulation of genomic errors, by studying the exact mode of DNA-segregation during their division. In this study, we demonstrated four lines of in vivo evidence in favor of cellular quiescence. Firstly, performing BrdU pulse-chase experiments, we localized ‘Label-Retaining Cells’ (LRCs). Secondly, EDU pulse-chase combined with Vasa labeling demonstrated the presence of neoblasts among the LRCs, while the majority of LRCs were differentiated cells.We showed that stem cells lose their label at a slow rate, indicating cellular quiescence. Thirdly, CldU/IdU− double labeling studies confirmed that label-retaining stem cells showed low proliferative activity. Finally, the use of the actin inhibitor, cytochalasin D, unequivocally demonstrated random segregation of DNA-strands in LRCs. Altogether, our data unambiguously demonstrated that the majority of neoblasts in M. lignano distribute their DNA randomly during cell division, and that label-retention is a direct result of cellular quiescence, rather than a sign of co-segregation of labeled strands.
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spelling pubmed-32618932012-01-24 Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano Verdoodt, Freija Willems, Maxime Mouton, Stijn De Mulder, Katrien Bert, Wim Houthoofd, Wouter Smith, Julian Ladurner, Peter PLoS One Research Article Adult stem cells are proposed to have acquired special features to prevent an accumulation of DNA-replication errors. Two such mechanisms, frequently suggested to serve this goal are cellular quiescence, and non-random segregation of DNA strands during stem cell division, a theory designated as the immortal strand hypothesis. To date, it has been difficult to test the in vivo relevance of both mechanisms in stem cell systems. It has been shown that in the flatworm Macrostomum lignano pluripotent stem cells (neoblasts) are present in adult animals. We sought to address by which means M. lignano neoblasts protect themselves against the accumulation of genomic errors, by studying the exact mode of DNA-segregation during their division. In this study, we demonstrated four lines of in vivo evidence in favor of cellular quiescence. Firstly, performing BrdU pulse-chase experiments, we localized ‘Label-Retaining Cells’ (LRCs). Secondly, EDU pulse-chase combined with Vasa labeling demonstrated the presence of neoblasts among the LRCs, while the majority of LRCs were differentiated cells.We showed that stem cells lose their label at a slow rate, indicating cellular quiescence. Thirdly, CldU/IdU− double labeling studies confirmed that label-retaining stem cells showed low proliferative activity. Finally, the use of the actin inhibitor, cytochalasin D, unequivocally demonstrated random segregation of DNA-strands in LRCs. Altogether, our data unambiguously demonstrated that the majority of neoblasts in M. lignano distribute their DNA randomly during cell division, and that label-retention is a direct result of cellular quiescence, rather than a sign of co-segregation of labeled strands. Public Library of Science 2012-01-19 /pmc/articles/PMC3261893/ /pubmed/22276162 http://dx.doi.org/10.1371/journal.pone.0030227 Text en Verdoodt 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
Verdoodt, Freija
Willems, Maxime
Mouton, Stijn
De Mulder, Katrien
Bert, Wim
Houthoofd, Wouter
Smith, Julian
Ladurner, Peter
Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano
title Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano
title_full Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano
title_fullStr Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano
title_full_unstemmed Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano
title_short Stem Cells Propagate Their DNA by Random Segregation in the Flatworm Macrostomum lignano
title_sort stem cells propagate their dna by random segregation in the flatworm macrostomum lignano
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261893/
https://www.ncbi.nlm.nih.gov/pubmed/22276162
http://dx.doi.org/10.1371/journal.pone.0030227
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