| Literature DB >> 30954439 |
Gui Ma1, Ang Gao1, Yinan Yang1, Yuan He1, Xi Zhang1, Baotong Zhang2, Zhiqian Zhang1, Mei Li3, Xing Fu1, Dan Zhao1, Rui Wu1, Leilei Qi1, Qingxia Hu1, Juan Li1, Liya Fu1, Zhengmao Zhu1, Jin-Tang Dong4.
Abstract
Progesterone (Pg)/progesterone receptor (PR) signaling drives mammary gland side-branching and alveologenesis, but the mechanisms through which Pg/PR signaling functions remain to be clarified. Using in vitro and in vivo models and histological and molecular analyses, we determined the role of Zfhx3 transcription factor in mammary gland development driven by Pg/PR signaling. Postnatal deletion of Zfhx3 in mouse mammary epithelial cells attenuated side-branching morphogenesis and alveologenesis. These effects were undetectable in the absence of Pg/PR signaling. During the estrus cycle, Zfhx3 expression corresponded to that of Pg, being at the highest level at the diestrus stage; Zfhx3 deletion inhibited mammary gland branching more potently at diestrus than estrus stage. Loss of Zfhx3 not only attenuated the expansion of stem/progenitor cells driven by Pg/PR signaling, but also impaired the function of Pg/PR signaling in the transcriptional activation of multiple genes. In addition, Pg/PR signaling significantly expanded PR- and Zfhx3-positive epithelial cells, and induced the physical association of ZFHX3 with PR. These findings establish Zfhx3 as an integral transcription factor of Pg/PR signaling in driving side-branching and alveologenesis during mammary gland development.Entities:
Keywords: Alveologenesis; Ductal side-branching; Mammary gland; Pregnancy; Progesterone-progesterone receptor signaling; Zfhx3/Atbf1
Year: 2019 PMID: 30954439 DOI: 10.1016/j.jgg.2019.03.003
Source DB: PubMed Journal: J Genet Genomics ISSN: 1673-8527 Impact factor: 4.275