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From the Cover: Cochaperone immunophilin FKBP52 is critical to uterine receptivity for embryo implantation

机译:从封面开始:Cochaperone亲免蛋白FKBP52对于胚胎植入的子宫接受性至关重要

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摘要

Embryo implantation in the uterus is a critical step in mammalian reproduction, requiring preparation of the uterus receptive to blastocyst implantation. Uterine receptivity, also known as the window of implantation, lasts for a limited period, and it is during this period blastocysts normally implant. Ovarian steroid hormones estrogen and progesterone (P4) are the primary regulators of this process. The immunophilin FKBP52 serves as a cochaperone for steroid hormone nuclear receptors to govern appropriate hormone action in target tissues. Here we show a critical role for FKBP52 in mouse implantation. This immunophilin has unique spatiotemporal expression in the uterus during implantation, and females missing the Fkbp52 gene have complete implantation failure due to lack of attainment of uterine receptivity. The overlapping uterine expression of FKBP52 with nuclear progesterone receptor (PR) in wild-type mice together with reduced P4 binding to PR, attenuated PR transcriptional activity and down-regulation of several P4-regulated genes in uteri of Fkbp52-/- mice, establishes this cochaperone as a critical regulator of uterine P4 function. Interestingly, ovulation, another P4-mediated event, remains normal. Collectively, the present investigation provides evidence for an in vivo role for this cochaperone in regulating tissue-specific hormone action and its critical role in uterine receptivity for implantation.
机译:子宫中的胚胎植入是哺乳动物繁殖的关键步骤,需要准备能够接受胚泡植入的子宫。子宫接受性,也称为植入窗口,持续有限的时间,并且在此期间,通常将胚泡植入。卵巢类固醇激素雌激素和孕酮(P4)是该过程的主要调节剂。亲免蛋白FKBP52充当类固醇激素核受体的伴侣蛋白来控制靶组织中适当的激素作用。在这里,我们展示了FKBP52在小鼠植入中的关键作用。这种亲免蛋白在植入过程中在子宫中具有独特的时空表达,并且缺少Fkbp52基因的雌性由于缺乏子宫接受性而完全植入失败。 FKBP52与核型孕酮受体(PR)在野生型小鼠中的子宫重叠表达,以及与PR的P4结合减少,PR转录活性减弱以及Fkbp52 -/-子宫中几个P4调控基因的下调小鼠,将这种伴侣蛋白确立为子宫P4功能的关键调节剂。有趣的是,排卵是另一种P4介导的事件,保持正常。总的来说,本研究提供了该伴侣分子在调节组织特异性激素作用中的体内作用及其在子宫植入中的关键作用的证据。

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