The pattern of β-catenin responsiveness within the mammary gland is regulated by progesterone receptor
Author(s) -
Minoti Hiremath,
John P. Lydon,
Pamela Cowin
Publication year - 2007
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.006585
Subject(s) - biology , mammary gland , beta catenin , endocrinology , progesterone receptor , catenin , progenitor cell , medicine , receptor , microbiology and biotechnology , progenitor , beta (programming language) , signal transduction , wnt signaling pathway , stem cell , cancer , estrogen receptor , genetics , breast cancer , computer science , programming language
Experiments involving beta-catenin loss- and gain-of-function in the mammary gland have decisively demonstrated the role of this protein in normal alveologenesis. However, the relationship between hormonal and beta-catenin signaling has not been investigated. In this study, we demonstrate that activated beta-catenin rescues alveologenesis in progesterone receptor (PR; Pgr)-null mice during pregnancy. Two distinct subsets of mammary cells respond to expression of DeltaN89beta-catenin. Cells at ductal tips are inherently beta-catenin-responsive and form alveoli in the absence of PR. However, PR activity confers beta-catenin responsiveness to progenitor cells along the lateral ductal borders in the virgin gland. Once activated by beta-catenin, responding cells switch on an alveolar differentiation program that is indistinguishable from that observed in pregnancy and is curtailed by PR signaling.
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