Form and Function: how Estrogen and Progesterone Regulate the Mammary Epithelial Hierarchy

被引:112
作者
Arendt, Lisa M. [1 ,2 ,3 ,4 ]
Kuperwasser, Charlotte [1 ,2 ,3 ,5 ]
机构
[1] Tufts Univ, Sackler Sch Grad Biomed Sci, Dev Mol & Chem Biol Dept, Sch Med, Boston, MA 02111 USA
[2] Tufts Med Ctr, Mol Oncol Res Inst, Boston, MA 02111 USA
[3] Raymond & Beverly Sackler Lab Convergence Biomed, Boston, MA 02111 USA
[4] Univ Wisconsin, Sch Vet Med, Dept Comparat Biosci, Madison, WI 53706 USA
[5] Tufts Univ, Sch Med, Dev Mol & Chem Biol Dept, Boston, MA 02111 USA
关键词
Mammary epithelial cells; Breast; Progenitor cells; Estrogen; Progesterone;
D O I
10.1007/s10911-015-9337-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The mammary gland undergoes dramatic post-natal growth beginning at puberty, followed by full development occurring during pregnancy and lactation. Following lactation, the alveoli undergo apoptosis, and the mammary gland reverses back to resemble the nonparous gland. This process of growth and regression occurs for multiple pregnancies, suggesting the presence of a hierarchy of stem and progenitor cells that are able to regenerate specialized populations of mammary epithelial cells. Expansion of epithelial cell populations in the mammary gland is regulated by ovarian steroids, in particular estrogen acting through its receptor estrogen receptor alpha (ER alpha) and progesterone signaling through progesterone receptor (PR). A diverse number of stem and progenitor cells have been identified based on expression of cell surface markers and functional assays. Here we review the current understanding of how estrogen and progesterone act together and separately to regulate stem and progenitor cells within the human and mouse mammary tissues. Better understanding of the hierarchal organization of epithelial cell populations in the mammary gland and how the hormonal milieu affects its regulation may provide important insights into the origins of different subtypes of breast cancer.
引用
收藏
页码:9 / 25
页数:17
相关论文
共 163 条
[81]
Stingl J., Eirew P., Ricketson I., Shackleton M., Vaillant F., Choi D., Et al., Purification and unique properties of mammary epithelial stem cells, Nature, 439, pp. 993-997, (2006)
[82]
Van Keymeulen A., Rocha A.S., Ousset M., Beck B., Bouvencourt G., Rock J., Et al., Distinct stem cells contribute to mammary gland development and maintenance, Nature, 479, pp. 189-193, (2011)
[83]
Prater M.D., Petit V., Alasdair R.I., Giraddi R.R., Shehata M., Menon S., Et al., Mammary stem cells have myoepithelial cell properties, Nat Cell Biol, 16, pp. 942-947, (2014)
[84]
Boras-Granic K., Dann P., Wysolmerski J.J., Embryonic cells contribute directly to the quiescent stem cell population in the adult mouse mammary gland, Breast Cancer Res, 16, (2014)
[85]
van Amerongen R., Bowman A.N., Nusse R., Developmental stage and time dictate the fate of Wnt/beta-catenin-responsive stem cells in the mammary gland, Cell Stem Cell, 11, pp. 387-400, (2012)
[86]
Wang D., Cai C., Dong X., Yu Q.C., Zhang X.O., Yang L., Et al., Identification of multipotent mammary stem cells by protein C receptor expression, Nature, 517, pp. 81-84, (2015)
[87]
Tao L., van Bragt M.P., Laudadio E., Li Z., Lineage tracing of mammary epithelial cells using cell-type-specific cre-expressing adenoviruses, Stem Cell Reports, 2, pp. 770-779, (2014)
[88]
Rios A.C., Fu N.Y., Lindeman G.J., Visvader J.E., In situ identification of bipotent stem cells in the mammary gland, Nature, 506, pp. 322-327, (2014)
[89]
Pei X.H., Bai F., Smith M.D., Usary J., Fan C., Pai S.Y., Et al., CDK inhibitor p18(INK4c) is a downstream target of GATA3 and restrains mammary luminal progenitor cell proliferation and tumorigenesis, Cancer Cell, 15, pp. 389-401, (2009)
[90]
Zhu Y., Huang Y.F., Kek C., Bulavin D.V., Apoptosis differently affects lineage tracing of Lgr5 and Bmi1 intestinal stem cell populations, Cell Stem Cell, 12, pp. 298-303, (2013)