<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saenz FR</submitter><funding>NCI NIH HHS</funding><pagination>e97666</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4022745</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(5)</volume><pubmed_abstract>Mammary epithelial (ME) cells cultured under conventional conditions senesce after several passages. Here, we demonstrate that mouse ME cells isolated from normal mammary glands or from mouse mammary tumor virus (MMTV)-Neu-induced mammary tumors, can be cultured indefinitely as conditionally reprogrammed cells (CRCs) on irradiated fibroblasts in the presence of the Rho kinase inhibitor Y-27632. Cell surface progenitor-associated markers are rapidly induced in normal mouse ME-CRCs relative to ME cells. However, the expression of certain mammary progenitor subpopulations, such as CD49f+ ESA+ CD44+, drops significantly in later passages. Nevertheless, mouse ME-CRCs grown in a three-dimensional extracellular matrix gave rise to mammary acinar structures. ME-CRCs isolated from MMTV-Neu transgen</pubmed_abstract><journal>PloS one</journal><pubmed_title>Conditionally reprogrammed normal and transformed mouse mammary epithelial cells display a progenitor-cell-like phenotype.</pubmed_title><pmcid>PMC4022745</pmcid><funding_grant_id>R21 CA180524</funding_grant_id><funding_grant_id>CA18052</funding_grant_id><funding_grant_id>CA177466</funding_grant_id><funding_grant_id>CA113477</funding_grant_id><funding_grant_id>R33 CA177466</funding_grant_id><funding_grant_id>P30 CA051008</funding_grant_id><funding_grant_id>P30CA051008</funding_grant_id><funding_grant_id>R01 CA113477</funding_grant_id><funding_grant_id>T32 CA009686</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Ory V</pubmed_authors><pubmed_authors>Wellstein A</pubmed_authors><pubmed_authors>Riegel AT</pubmed_authors><pubmed_authors>Saenz FR</pubmed_authors><pubmed_authors>Rosenfield S</pubmed_authors><pubmed_authors>Schlegel R</pubmed_authors><pubmed_authors>Johnson MD</pubmed_authors><pubmed_authors>AlOtaiby M</pubmed_authors><pubmed_authors>Furlong M</pubmed_authors><pubmed_authors>Cavalli LR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Conditionally reprogrammed normal and transformed mouse mammary epithelial cells display a progenitor-cell-like phenotype.</name><description>Mammary epithelial (ME) cells cultured under conventional conditions senesce after several passages. Here, we demonstrate that mouse ME cells isolated from normal mammary glands or from mouse mammary tumor virus (MMTV)-Neu-induced mammary tumors, can be cultured indefinitely as conditionally reprogrammed cells (CRCs) on irradiated fibroblasts in the presence of the Rho kinase inhibitor Y-27632. Cell surface progenitor-associated markers are rapidly induced in normal mouse ME-CRCs relative to ME cells. However, the expression of certain mammary progenitor subpopulations, such as CD49f+ ESA+ CD44+, drops significantly in later passages. Nevertheless, mouse ME-CRCs grown in a three-dimensional extracellular matrix gave rise to mammary acinar structures. ME-CRCs isolated from MMTV-Neu transgen</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-18T20:55:43.505Z</modification><creation>2019-03-26T23:24:50Z</creation></dates><accession>S-EPMC4022745</accession><cross_references><pubmed>24831228</pubmed><doi>10.1371/journal.pone.0097666</doi></cross_references></HashMap>