The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
Amphiregulin is an essential mediator of estrogen receptor α function in mammary gland development
Open accessAbstract
Most mammary gland development occurs after birth under the control of systemic hormones. Estrogens induce mammary epithelial cell proliferation during puberty via epithelial estrogen receptor α (ERα) by a paracrine mechanism. Epidermal growth factor receptor (EGFR) signaling has long been implicated downstream of ERα signaling, and several EGFR ligands have been described as estrogen-target genes in tumor cell lines. Here, we show that amphiregulin is the unique EGF family member to be transcriptionally induced by estrogen in the mammary glands of puberal mice at a time of exponential expansion of the ductal system. In fact, we find that estrogens induce amphiregulin through the ERα and require amphiregulin to induce proliferation of the mammary epithelium. Like ERα, amphiregulin is required in the epithelium of puberal mice for epithelial proliferation, terminal end buds formation, and ductal elongation. Subsequent stages, such as side-branching and alveologenesis, are not affected. When amphiregulin −/− mammary epithelial cells are in close vicinity to wild-type cells, they proliferate and contribute to all cell compartments of the ductal outgrowth. Thus, amphiregulin is an important paracrine mediator of estrogen function specifically required for puberty-induced ductal elongation, but not for any earlier or later developmental stages.
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Cites
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Control of mammary stem cell function by steroid hormone signalling
Asselin-Labat, M.-L., Vaillant, F., Sheridan, J. M., Pal, B., Wu, D., Simpson, E. R., Yasuda, H., Smyth, G. K., Martin, T. J., Lindeman, G. J., et al. (2010) · Nature · doi:10.1038/nature09027 · Cited by 693
Phenotypic and functional characterisation of the luminal cell hierarchy of the mammary gland
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Sculpting Organs: Mechanical Regulation of Tissue Development
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Human Breast Progenitor Cell Numbers Are Regulated by WNT and TBX3
Arendt, L. M., St. Laurent, J., Wronski, A., Caballero, S., Lyle, S. R., Naber, S. P., & Kuperwasser, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111442 · Cited by 27
Metadata
- Authors
- Ciarloni, L., Mallepell, S., & Brisken, C.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2007-03-27
- Volume
- 104
- Issue
- 13
- Pages
- 5455-5460
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2134318982
- Cited by
- 316
- References
- 46
- FWCI
- 10.05
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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