| Literature DB >> 25173976 |
Michael D Prater1, Valérie Petit2, I Alasdair Russell1, Rajshekhar R Giraddi1, Mona Shehata1, Suraj Menon1, Reiner Schulte1, Ivo Kalajzic3, Nicola Rath4, Michael F Olson4, Daniel Metzger5, Marisa M Faraldo2, Marie-Ange Deugnier2, Marina A Glukhova2, John Stingl1.
Abstract
Contractile myoepithelial cells dominate the basal layer of the mammary epithelium and are considered to be differentiated cells. However, we observe that up to 54% of single basal cells can form colonies when seeded into adherent culture in the presence of agents that disrupt actin-myosin interactions, and on average, 65% of the single-cell-derived basal colonies can repopulate a mammary gland when transplanted in vivo. This indicates that a high proportion of basal myoepithelial cells can give rise to a mammary repopulating unit (MRU). We demonstrate that myoepithelial cells, flow-sorted using two independent myoepithelial-specific reporter strategies, have MRU capacity. Using an inducible lineage-tracing approach we follow the progeny of myoepithelial cells that express α-smooth muscle actin and show that they function as long-lived lineage-restricted stem cells in the virgin state and during pregnancy.Entities:
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Year: 2014 PMID: 25173976 PMCID: PMC4183554 DOI: 10.1038/ncb3025
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824