Characterization of bipotent mammary epithelial progenitor cells in normal adult human breast tissue

J Stingl, CJ Eaves, I Zandieh, JT Emerman - Breast cancer research and …, 2001 - Springer
J Stingl, CJ Eaves, I Zandieh, JT Emerman
Breast cancer research and treatment, 2001Springer
The purpose of the present study was to characterize primitive epithelial progenitor
populations present in adult normal human mammary tissue using a combination of flow
cytometry and in vitro colony assay procedures. Three types of human breast epithelial cell
(HBEC) progenitors were identified: luminal-restricted, myoepithelial-restricted and bipotent
progenitors. The first type expressed epithelial cell adhesion molecule (EpCAM), α6 integrin
and MUC1 and generated colonies composed exclusively of cells positive for the luminal …
Abstract
The purpose of the present study was to characterize primitive epithelial progenitor populations present in adult normal human mammary tissue using a combination of flow cytometry and in vitro colony assay procedures. Three types of human breast epithelial cell (HBEC) progenitors were identified: luminal-restricted, myoepithelial-restricted and bipotent progenitors. The first type expressed epithelial cell adhesion molecule (EpCAM), α6 integrin and MUC1 and generated colonies composed exclusively of cells positive for the luminal-associated markers keratin 8/18, keratin 19, EpCAM and MUC1. Bipotent progenitors produced colonies containing a central core of cells expressing luminal markers surrounded by keratin 14+ myoepithelial-like cells. Single cell cultures confirmed the bipotentiality of these progenitors. Their high expression of α6 integrin and low expression of MUC1 suggests a basal position of these cells in the mammary epithelium in vivo. Serial passage in vitro of an enriched population of bipotent progenitors demonstrated that only myoepithelial-restricted progenitors could be readily generated under the culture conditions used. These results support a hierarchical branching model of HBEC progenitor differentiation from a primitive uncommitted cell to luminal- and myoepithelial-restricted progenitors.
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