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一种经过基因工程改造以条件性表达孕激素受体-B亚型的小鼠模型。

A mouse model engineered to conditionally express the progesterone receptor-B isoform.

作者信息

Hai Lan, Szwarc Maria M, Wetendorf Margeaux, Wu San-Pin, Peavey Mary C, Grimm Sandra L, Edwards Dean P, DeMayo Francesco J, Lydon John P

机构信息

Department of Molecular & Cellular Biology, Baylor College of Medicine, Houston, Texas.

University of North Carolina Chapel Hill, Chapel Hill, North Carolina.

出版信息

Genesis. 2018 Aug;56(8):e23223. doi: 10.1002/dvg.23223. Epub 2018 Aug 10.

Abstract

Using a Rosa26 gene targeting strategy in mouse embryonic stem cells, we have generated a new transgenic mouse (Pgr-B ), 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 mouse with the MMTV-CREA transgenic mouse to create the MMTV-CREA/Pgr-B 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 mouse to examine the role of the PGR-B isoform in different physiologic and pathophysiologic systems that are responsive to progesterone.

摘要

利用小鼠胚胎干细胞中的Rosa26基因靶向策略,我们培育出了一种新的转基因小鼠(Pgr-B ),其设计目的是在与特定的cre驱动小鼠杂交时,条件性表达带有表位标签的小鼠孕激素受体-B(PGR-B)亚型。为了在功能上验证这种转基因小鼠,我们将Pgr-B 小鼠与MMTV-CREA转基因小鼠杂交,创造出了MMTV-CREA/Pgr-B 双转基因小鼠(称为PR-B:OE,以表示PGR-B过表达小鼠)。正如预期的那样,转基因衍生的PGR-B蛋白特异性地靶向处女乳腺上皮。在功能水平上,PR-B:OE双转基因小鼠表现出异常的乳腺形态发生——扩张的上皮导管、早熟的腺泡形成和侧向分支,同时伴有显著的增殖特征——这导致怀孕的PR-B:OE小鼠在分娩时无法表现出乳腺终末分化。由于这种发育失败,PR-B:OE乳腺无法产奶,导致原本健康的一窝幼崽在新生儿早期死亡。这第一系列分析证明了Pgr-B 小鼠在研究PGR-B亚型在对孕激素有反应的不同生理和病理生理系统中的作用方面的实用性。

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