z-logo
open-access-imgOpen Access
Cell Hierarchy and Lineage Commitment in the Bovine Mammary Gland
Author(s) -
Gat Rauner,
Itamar Barash
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0030113
Subject(s) - biology , progenitor cell , microbiology and biotechnology , population , stem cell , myoepithelial cell , transdifferentiation , cellular differentiation , cell type , mammary gland , cell sorting , cell , cell culture , lineage markers , immunology , genetics , gene , immunohistochemistry , demography , cancer , sociology , breast cancer
The bovine mammary gland is a favorable organ for studying mammary cell hierarchy due to its robust milk-production capabilities that reflect the adaptation of its cell populations to extensive expansion and differentiation. It also shares basic characteristics with the human breast, and identification of its cell composition may broaden our understanding of the diversity in cell hierarchy among mammals. Here, Lin − epithelial cells were sorted according to expression of CD24 and CD49f into four populations: CD24 med CD49f pos (putative stem cells, puStm), CD24 neg CD49f pos (Basal), CD24 high CD49f neg (putative progenitors, puPgt) and CD24 med CD49f neg (luminal, Lum). These populations maintained differential gene expression of lineage markers and markers of stem cells and luminal progenitors. Of note was the high expression of Stat5a in the puPgt cells, and of Notch1, Delta1, Jagged1 and Hey1 in the puStm and Basal populations. Cultured puStm and Basal cells formed lineage-restricted basal or luminal clones and after re-sorting, colonies that preserved a duct-like alignment of epithelial layers. In contrast, puPgt and Lum cells generated only luminal clones and unorganized colonies. Under non-adherent culture conditions, the puPgt and puStm populations generated significantly more floating colonies. The increase in cell number during culture provides a measure of propagation potential, which was highest for the puStm cells. Taken together, these analyses position puStm cells at the top of the cell hierarchy and denote the presence of both bi-potent and luminally restricted progenitors. In addition, a population of differentiated luminal cells was marked. Finally, combining ALDH activity with cell-surface marker analyses defined a small subpopulation that is potentially stem cell- enriched.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom