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...

Full description

Bibliographic Details
Main Authors: Freija Verdoodt, Maxime Willems, Stijn Mouton, Katrien De Mulder, Wim Bert, Wouter Houthoofd, Julian Smith, Peter Ladurner
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3261893?pdf=render
_version_ 1828749988848467968
author Freija Verdoodt
Maxime Willems
Stijn Mouton
Katrien De Mulder
Wim Bert
Wouter Houthoofd
Julian Smith
Peter Ladurner
author_facet Freija Verdoodt
Maxime Willems
Stijn Mouton
Katrien De Mulder
Wim Bert
Wouter Houthoofd
Julian Smith
Peter Ladurner
author_sort Freija Verdoodt
collection DOAJ
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.
first_indexed 2024-12-10T20:31:31Z
format Article
id doaj.art-2e16d0539192401eb745f59f79f97b1c
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-10T20:31:31Z
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-2e16d0539192401eb745f59f79f97b1c2022-12-22T01:34:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e3022710.1371/journal.pone.0030227Stem cells propagate their DNA by random segregation in the flatworm Macrostomum lignano.Freija VerdoodtMaxime WillemsStijn MoutonKatrien De MulderWim BertWouter HouthoofdJulian SmithPeter LadurnerAdult 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.http://europepmc.org/articles/PMC3261893?pdf=render
spellingShingle Freija Verdoodt
Maxime Willems
Stijn Mouton
Katrien De Mulder
Wim Bert
Wouter Houthoofd
Julian Smith
Peter Ladurner
Stem cells propagate their DNA by random segregation in the flatworm Macrostomum lignano.
PLoS ONE
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
url http://europepmc.org/articles/PMC3261893?pdf=render
work_keys_str_mv AT freijaverdoodt stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT maximewillems stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT stijnmouton stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT katriendemulder stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT wimbert stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT wouterhouthoofd stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT juliansmith stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano
AT peterladurner stemcellspropagatetheirdnabyrandomsegregationintheflatwormmacrostomumlignano