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Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice

Hematopoietic stem cells (HSCs) continuously replenish all blood cell types through a series of differentiation steps and repeated cell divisions that involve the generation of lineage-committed progenitors. However, whether cell division in HSCs precedes differentiation is unclear. To this end, we...

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Autores principales: Grinenko, Tatyana, Eugster, Anne, Thielecke, Lars, Ramasz, Beáta, Krüger, Anja, Dietz, Sevina, Glauche, Ingmar, Gerbaulet, Alexander, von Bonin, Malte, Basak, Onur, Clevers, Hans, Chavakis, Triantafyllos, Wielockx, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954009/
https://www.ncbi.nlm.nih.gov/pubmed/29765026
http://dx.doi.org/10.1038/s41467-018-04188-7
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author Grinenko, Tatyana
Eugster, Anne
Thielecke, Lars
Ramasz, Beáta
Krüger, Anja
Dietz, Sevina
Glauche, Ingmar
Gerbaulet, Alexander
von Bonin, Malte
Basak, Onur
Clevers, Hans
Chavakis, Triantafyllos
Wielockx, Ben
author_facet Grinenko, Tatyana
Eugster, Anne
Thielecke, Lars
Ramasz, Beáta
Krüger, Anja
Dietz, Sevina
Glauche, Ingmar
Gerbaulet, Alexander
von Bonin, Malte
Basak, Onur
Clevers, Hans
Chavakis, Triantafyllos
Wielockx, Ben
author_sort Grinenko, Tatyana
collection PubMed
description Hematopoietic stem cells (HSCs) continuously replenish all blood cell types through a series of differentiation steps and repeated cell divisions that involve the generation of lineage-committed progenitors. However, whether cell division in HSCs precedes differentiation is unclear. To this end, we used an HSC cell-tracing approach and Ki67(RFP) knock-in mice, in a non-conditioned transplantation model, to assess divisional history, cell cycle progression, and differentiation of adult HSCs. Our results reveal that HSCs are able to differentiate into restricted progenitors, especially common myeloid, megakaryocyte-erythroid and pre-megakaryocyte progenitors, without undergoing cell division and even before entering the S phase of the cell cycle. Additionally, the phenotype of the undivided but differentiated progenitors correlated with the expression of lineage-specific genes and loss of multipotency. Thus HSC fate decisions can be uncoupled from physical cell division. These results facilitate a better understanding of the mechanisms that control fate decisions in hematopoietic cells.
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spelling pubmed-59540092018-05-17 Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice Grinenko, Tatyana Eugster, Anne Thielecke, Lars Ramasz, Beáta Krüger, Anja Dietz, Sevina Glauche, Ingmar Gerbaulet, Alexander von Bonin, Malte Basak, Onur Clevers, Hans Chavakis, Triantafyllos Wielockx, Ben Nat Commun Article Hematopoietic stem cells (HSCs) continuously replenish all blood cell types through a series of differentiation steps and repeated cell divisions that involve the generation of lineage-committed progenitors. However, whether cell division in HSCs precedes differentiation is unclear. To this end, we used an HSC cell-tracing approach and Ki67(RFP) knock-in mice, in a non-conditioned transplantation model, to assess divisional history, cell cycle progression, and differentiation of adult HSCs. Our results reveal that HSCs are able to differentiate into restricted progenitors, especially common myeloid, megakaryocyte-erythroid and pre-megakaryocyte progenitors, without undergoing cell division and even before entering the S phase of the cell cycle. Additionally, the phenotype of the undivided but differentiated progenitors correlated with the expression of lineage-specific genes and loss of multipotency. Thus HSC fate decisions can be uncoupled from physical cell division. These results facilitate a better understanding of the mechanisms that control fate decisions in hematopoietic cells. Nature Publishing Group UK 2018-05-15 /pmc/articles/PMC5954009/ /pubmed/29765026 http://dx.doi.org/10.1038/s41467-018-04188-7 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Grinenko, Tatyana
Eugster, Anne
Thielecke, Lars
Ramasz, Beáta
Krüger, Anja
Dietz, Sevina
Glauche, Ingmar
Gerbaulet, Alexander
von Bonin, Malte
Basak, Onur
Clevers, Hans
Chavakis, Triantafyllos
Wielockx, Ben
Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
title Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
title_full Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
title_fullStr Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
title_full_unstemmed Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
title_short Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
title_sort hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954009/
https://www.ncbi.nlm.nih.gov/pubmed/29765026
http://dx.doi.org/10.1038/s41467-018-04188-7
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