IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v542y2017i7641d10.1038_nature21046.html
   My bibliography  Save this article

Identity and dynamics of mammary stem cells during branching morphogenesis

Author

Listed:
  • Colinda L. G. J. Scheele

    (Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht)

  • Edouard Hannezo

    (Cavendish Laboratory, University of Cambridge
    The Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge
    The Wellcome Trust/Medical Research Council Stem Cell Institute, University of Cambridge)

  • Mauro J. Muraro

    (Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht)

  • Anoek Zomer

    (Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht)

  • Nathalia S. M. Langedijk

    (Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht)

  • Alexander van Oudenaarden

    (Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht)

  • Benjamin D. Simons

    (Cavendish Laboratory, University of Cambridge
    The Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge
    The Wellcome Trust/Medical Research Council Stem Cell Institute, University of Cambridge)

  • Jacco van Rheenen

    (Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht)

Abstract

During puberty, the mouse mammary gland develops into a highly branched epithelial network. Owing to the absence of exclusive stem cell markers, the location, multiplicity, dynamics and fate of mammary stem cells (MaSCs), which drive branching morphogenesis, are unknown. Here we show that morphogenesis is driven by proliferative terminal end buds that terminate or bifurcate with near equal probability, in a stochastic and time-invariant manner, leading to a heterogeneous epithelial network. We show that the majority of terminal end bud cells function as highly proliferative, lineage-committed MaSCs that are heterogeneous in their expression profile and short-term contribution to ductal extension. Yet, through cell rearrangements during terminal end bud bifurcation, each MaSC is able to contribute actively to long-term growth. Our study shows that the behaviour of MaSCs is not directly linked to a single expression profile. Instead, morphogenesis relies upon lineage-restricted heterogeneous MaSC populations that function as single equipotent pools in the long term.

Suggested Citation

  • Colinda L. G. J. Scheele & Edouard Hannezo & Mauro J. Muraro & Anoek Zomer & Nathalia S. M. Langedijk & Alexander van Oudenaarden & Benjamin D. Simons & Jacco van Rheenen, 2017. "Identity and dynamics of mammary stem cells during branching morphogenesis," Nature, Nature, vol. 542(7641), pages 313-317, February.
  • Handle: RePEc:nat:nature:v:542:y:2017:i:7641:d:10.1038_nature21046
    DOI: 10.1038/nature21046
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature21046
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature21046?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
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

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


    Cited by:

    1. Bryant, Adam S. & Lavrentovich, Maxim O., 2022. "Survival in branching cellular populations," Theoretical Population Biology, Elsevier, vol. 144(C), pages 13-23.

    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:nature:v:542:y:2017:i:7641:d:10.1038_nature21046. 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.