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SCA-1 Labels a Subset of Estrogen-Responsive Bipotential Repopulating Cells within the CD24+ CD49fhi Mammary Stem Cell-Enriched Compartment.


ABSTRACT: Estrogen stimulates breast development during puberty and mammary tumors in adulthood through estrogen receptor-? (ER?). These effects are proposed to occur via ER?+ luminal cells and not the mammary stem cells (MaSCs) that are ER?neg. Since ER?+ luminal cells express stem cell antigen-1 (SCA-1), we sought to determine if SCA-1 could define an ER?+ subset of EpCAM+/CD24+/CD49fhi MaSCs. We show that the MaSC population has a distinct SCA-1+ population that is abundant in pre-pubertal mammary glands. The SCA-1+ MaSCs have less stem cell markers and less in vivo repopulating activity than their SCA-1neg counterparts. However, they express ER? and specifically enter the cell cycle at puberty. Using estrogen-deficient aromatase knockouts (ArKO), we showed that the SCA-1+ MaSC could be directly modulated by estrogen supplementation. Thus, SCA-1 enriches for an ER?+, estrogen-sensitive subpopulation within the CD24+/CD49fhi MaSC population that may be responsible for the hormonal sensitivity of the developing mammary gland.

SUBMITTER: Dall GV 

PROVIDER: S-EPMC5312257 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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SCA-1 Labels a Subset of Estrogen-Responsive Bipotential Repopulating Cells within the CD24<sup>+</sup> CD49f<sup>hi</sup> Mammary Stem Cell-Enriched Compartment.

Dall Genevieve V GV   Vieusseux Jessica L JL   Korach Kenneth S KS   Arao Yukitomo Y   Hewitt Sylvia C SC   Hamilton Katherine J KJ   Dzierzak Elaine E   Boon Wah Chin WC   Simpson Evan R ER   Ramsay Robert G RG   Stein Torsten T   Morris Joanne S JS   Anderson Robin L RL   Risbridger Gail P GP   Britt Kara L KL  

Stem cell reports 20170126 2


Estrogen stimulates breast development during puberty and mammary tumors in adulthood through estrogen receptor-α (ERα). These effects are proposed to occur via ERα<sup>+</sup> luminal cells and not the mammary stem cells (MaSCs) that are ERα<sup>neg</sup>. Since ERα<sup>+</sup> luminal cells express stem cell antigen-1 (SCA-1), we sought to determine if SCA-1 could define an ERα<sup>+</sup> subset of EpCAM<sup>+</sup>/CD24<sup>+</sup>/CD49f<sup>hi</sup> MaSCs. We show that the MaSC population h  ...[more]

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