Identity and dynamics of mammary stem cells during branching morphogenesis

Colinda L. G. J. Scheele, Edouard Hannezo, Mauro J. Muraro, Anoek Zomer, Nathalia S. M. Langedijk, Alexander van Oudenaarden, Benjamin D. Simons () and Jacco van Rheenen ()
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Colinda L. G. J. Scheele: Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht
Edouard Hannezo: Cavendish Laboratory, 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
Jacco van Rheenen: Cancer Genomics Netherlands, Hubrecht Institute-KNAW & University Medical Centre Utrecht

Nature, 2017, vol. 542, issue 7641, 313-317

Abstract: 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.

Date: 2017
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DOI: 10.1038/nature21046

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