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dc.contributor.authorThomas, E.
dc.contributor.authorLee-Pullen, T.
dc.contributor.authorRigby, P.
dc.contributor.authorHartmann, P.
dc.contributor.authorXu, J.
dc.contributor.authorZeps, Nikolajs
dc.date.accessioned2017-01-30T15:18:34Z
dc.date.available2017-01-30T15:18:34Z
dc.date.created2015-10-29T04:09:34Z
dc.date.issued2012
dc.identifier.citationThomas, E. and Lee-Pullen, T. and Rigby, P. and Hartmann, P. and Xu, J. and Zeps, N. 2012. Receptor activator of NF-κB ligand promotes proliferation of a putative mammary stem cell unique to the lactating epithelium. Stem Cells. 30 (6): pp. 1255-1264.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/45110
dc.identifier.doi10.1002/stem.1092
dc.description.abstract

In mice, CD49fhi mammary stem cells (MaSCs) asymmetrically divide to generate CD49f+ committed progenitor cells that differentiate into CD49f− phenotypes of the milk-secreting tissue at the onset of pregnancy. We show CD49f+ primary mammary epithelial cells (PMECs) isolated from lactating tissue uniquely respond to pregnancy-associated hormones (PAH) compared with CD49f+ cells from nonlactating tissue. Differentiation of CD49f+ PMEC in extracellular matrix produces CD49f− luminal cells to form differentiated alveoli. The PAH prolactin and placental lactogen specifically stimulate division of CD49f− luminal cells, while receptor activator of nuclear factor (NF)-κB ligand (RANKL) specifically stimulates division of basal CD49f+ cells. In nondifferentiating conditions, we observed a greater proportion of multipotent self-renewing cells, and RANKL treatment activated the RANK pathway in these cultures. Furthermore, we observed the deposition of calcium nodules in a proportion of these cells. These data imply that a MaSC unique to the lactating breast exists in humans, which generates progeny with discrete lineages and distinct response to PAH.

dc.titleReceptor activator of NF-κB ligand promotes proliferation of a putative mammary stem cell unique to the lactating epithelium
dc.typeJournal Article
dcterms.source.volume30
dcterms.source.number6
dcterms.source.startPage1255
dcterms.source.endPage1264
dcterms.source.issn1066-5099
dcterms.source.titleStem Cells
curtin.accessStatusOpen access via publisher


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