IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v9y2018i1d10.1038_s41467-018-04188-7.html
   My bibliography  Save this article

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

Author

Listed:
  • Tatyana Grinenko

    (Technische Universität Dresden)

  • Anne Eugster

    (Technische Universität Dresden)

  • Lars Thielecke

    (Technische Universität Dresden)

  • Beáta Ramasz

    (Technische Universität Dresden)

  • Anja Krüger

    (Technische Universität Dresden)

  • Sevina Dietz

    (Technische Universität Dresden)

  • Ingmar Glauche

    (Technische Universität Dresden)

  • Alexander Gerbaulet

    (Technische Universität Dresden)

  • Malte Bonin

    (Technische Universität Dresden
    partner site Dresden
    German Cancer Research Center (DKFZ))

  • Onur Basak

    (Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht
    UMC Utrecht
    University Medical Center Utrecht and Utrecht University)

  • Hans Clevers

    (Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht
    UMC Utrecht
    Lundlaan 6)

  • Triantafyllos Chavakis

    (Technische Universität Dresden
    Technische Universität Dresden)

  • Ben Wielockx

    (Technische Universität Dresden
    Technische Universität Dresden)

Abstract

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 Ki67RFP 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.

Suggested Citation

  • Tatyana Grinenko & Anne Eugster & Lars Thielecke & Beáta Ramasz & Anja Krüger & Sevina Dietz & Ingmar Glauche & Alexander Gerbaulet & Malte Bonin & Onur Basak & Hans Clevers & Triantafyllos Chavakis &, 2018. "Hematopoietic stem cells can differentiate into restricted myeloid progenitors before cell division in mice," Nature Communications, Nature, vol. 9(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04188-7
    DOI: 10.1038/s41467-018-04188-7
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-018-04188-7
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-018-04188-7?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Jacqueline Feyen & Zhen Ping & Lanpeng Chen & Claire Dijk & Tim V. D. Tienhoven & Paulina M. H. Strien & Remco M. Hoogenboezem & Michiel J. W. Wevers & Mathijs A. Sanders & Ivo P. Touw & Marc H. G. P., 2022. "Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04188-7. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.