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雌激素激素生理学:雌激素受体突变小鼠的生殖研究结果。

Estrogen hormone physiology: reproductive findings from estrogen receptor mutant mice.

机构信息

Receptor Biology Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences/NIH, Research Triangle Park, NC 27709, United States.

Receptor Biology Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences/NIH, Research Triangle Park, NC 27709, United States.

出版信息

Reprod Biol. 2014 Mar;14(1):3-8. doi: 10.1016/j.repbio.2013.12.002. Epub 2013 Dec 21.

Abstract

Estrogen receptors (ERs) play a crucial role in reproduction and normal physiology. The two sub-types of ER (ERα and β) are expressed in various levels in different tissues and selective cell types. Gene targeting technology allowed us to produce lines of mice with disrupted ERα (αERKO) and ERβ genes (βERKO) as well as a compound αβERKO in the whole body. Male and female αERKO mice are infertile. Estrogen, EGF and IGF-1 treatments failed to induce uterine growth and DNA synthesis in αERKO uteri. αERKO females are infertile due to hypoplastic uteri and hyperemic ovaries with no corpora lutea due to persistent LH stimulation from loss of negative feedback. αERKO males are infertile, with testicular atrophy and seminiferous tubule dysmorphogenesis producing decreased spermatogenesis and inactive sperm. βERKO females show arrested folliculogenesis and subfertility. Ovarian analyses indicate differential gene expression related to ovulatory stimulation deficits including lack of LH, PR, Cyp19 and Cox2 expression. A unique ovarian phenotype is found only in αβERKO females showing transdifferentiation of granulosa cells to Sertoli cells. We describe here several novel mouse models which possess ERα gene modification. To understand ERα function in uterine endometrial epithelial cells, we generated a tissue selective ERα gene disrupted mouse model, the uterine epithelial-specific ERα knockout (UtEpiαERKO). To understand the physiological role of ERα functional domains, we generated a mouse model with a mutation in the ligand dependent transcription activation domain of ERα (AF2ERKI). Findings from the ERα mutant mice suggest that the absence of functional ERα is not lethal and results in significant endocrine effects and altered physiological processes.

摘要

雌激素受体(ERs)在生殖和正常生理中起着至关重要的作用。两种 ER 亚型(ERα和 ERβ)在不同组织和选择性细胞类型中以不同水平表达。基因靶向技术使我们能够产生 ERα(αERKO)和 ERβ基因(βERKO)缺失以及全身αβERKO 的小鼠品系。雄性和雌性αERKO 小鼠不育。雌激素、EGF 和 IGF-1 处理未能诱导 αERKO 子宫的生长和 DNA 合成。由于子宫发育不良和卵巢充血,没有黄体由于 LH 刺激的持续失去负反馈,αERKO 雌性不育。αERKO 雄性不育,睾丸萎缩和曲细精管发育不良导致精子发生减少和精子失活。βERKO 雌性表现为卵泡发生停滞和生育力下降。卵巢分析表明与排卵刺激缺陷相关的差异基因表达,包括缺乏 LH、PR、Cyp19 和 Cox2 表达。仅在 αβERKO 雌性中发现一种独特的卵巢表型,表现为颗粒细胞向支持细胞的转分化。我们在这里描述了几种具有 ERα 基因修饰的新型小鼠模型。为了了解 ERα 在子宫子宫内膜上皮细胞中的功能,我们生成了组织选择性 ERα 基因缺失的小鼠模型,即子宫上皮特异性 ERα 敲除(UtEpiαERKO)。为了了解 ERα 功能域的生理作用,我们生成了一种具有 ERα 配体依赖性转录激活域突变的小鼠模型(AF2ERKI)。从 ERα 突变小鼠的研究结果表明,缺乏功能性 ERα 并不是致命的,并且会导致显著的内分泌效应和改变的生理过程。

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