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
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