| Literature DB >> 30004627 |
Lan Hai1, Maria M Szwarc1, Margeaux Wetendorf2, San-Pin Wu3, Mary C Peavey4, Sandra L Grimm1, Dean P Edwards1, Francesco J DeMayo3, John P Lydon1.
Abstract
Using a Rosa26 gene targeting strategy in mouse embryonic stem cells, we have generated a new transgenic mouse (Pgr-B LSL ), which is designed to conditionally express the epitope-tagged mouse progesterone receptor-B (PGR-B) isoform when crossed with a specific cre driver mouse. To functionally validate this transgenic mouse, we crossed the Pgr-B LSL mouse with the MMTV-CREA transgenic mouse to create the MMTV-CREA/Pgr-B LSL bigenic (termed PR-B:OE to denote PGR-B overexpressor). As expected, transgene-derived PGR-B protein was specifically targeted to the virgin mammary gland epithelium. At a functional level, the PR-B:OE bigenic exhibited abnormal mammary morphogenesis-dilated epithelial ducts, precocious alveologenesis and lateral side-branching, along with a prominent proliferative signature-that resulted in pregnant PR-B:OE mice unable to exhibit mammary gland terminal differentiation at parturition. Because of this developmental failure, the PR-B:OE mammary gland was incapable of producing milk resulting in early neonatal death of otherwise healthy litters. This first line of analysis demonstrates the utility of the Pgr-B LSL mouse to examine the role of the PGR-B isoform in different physiologic and pathophysiologic systems that are responsive to progesterone.Entities:
Keywords: differentiation; isoform; lactation; mammary gland; mouse; progesterone receptor-B; proliferation; transgenic
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Year: 2018 PMID: 30004627 PMCID: PMC6141023 DOI: 10.1002/dvg.23223
Source DB: PubMed Journal: Genesis ISSN: 1526-954X Impact factor: 2.487