Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 103, Issue 7, Pages 2196-2201Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.0510974103
Keywords
transactivation function 1; epithelial-mesenchymal interactions; branching; hormonal control; tissue recombination
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Estradiol is a major regulator of postnatal mammary gland development and thought to exert its effects through estrogen receptor alpha (ER alpha) expressed in the mammary gland stroma and epithelium. Previous studies, however, were confounded by the use of an ERa mutant strain that retains some of the protein with transactivation activity. Here, we use an ER alpha(-/-) mouse strain in which no ERa transcript can be detected to analyze mammary gland development in the complete absence of ERa signaling. The ER alpha(-/-) females show no development beyond a rudimentary ductal system. By grafting ER alpha(-/-) epithelium or stroma in combination with ER alpha WT stroma or epithelium, we show that the primary target for estradiol is the mammary epithelium, whereas a direct response of the mammary stroma is not required for mammary gland development to proceed normally. Mammary glands reconstituted with ER alpha(-/-) mammary epithelium exposed to pregnancy hormones show increased transcription of milk protein genes, indicating that ER alpha signaling is not an absolute requirement for a transcriptional response to pregnancy hormones. When ER alpha(-/-) mammary epithelial cells are in close vicinity to ER alpha WT cells, they proliferate and contribute to all aspects of mammary gland development, indicating that estradiol, like progesterone, orchestrates proliferation and morphogenesis by a paracrine mechanism, affecting nearby cells in the mammary epithelium.
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