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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >The reproductive phenotype of mice null for transcription factor Krüppel-like factor 13 suggests compensatory function of family member Krüppel-like factor 9 in the peri-implantation uterus
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The reproductive phenotype of mice null for transcription factor Krüppel-like factor 13 suggests compensatory function of family member Krüppel-like factor 9 in the peri-implantation uterus

机译:转录因子Krüppel样因子13无效的小鼠的生殖表型暗示着家族成员Krüppel样因子9在围着子宫中的补偿功能。

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The ovarian hormones estrogen and progesterone promote uterine receptivity and successful pregnancy through their cognate receptors functioning in concert with context-dependent nuclear coregulators. Previously, we showed that the transcription factor Krüppel-like factor (KLF) 9 is a progesterone receptor (PGR) coactivator in the uterus and that mice null for Klf9 exhibit subfertility and reduced progesterone sensitivity. The highly related family member KLF13 displays increased expression in uteri of pregnant and nonpregnant Klf9 null mice and similarly regulates PGR-mediated transactivation in endometrial stromal cells. However, a uterine phenotype with loss of Klf13 has not been reported. In the present study, we demonstrate that Klf13 deficiency in mice did not compromise female fertility and pregnancy outcome. Klf13 null females had litter sizes, numbers of implanting embryos, uterine morphology, and ovarian steroid hormone production comparable to those of wild-type (WT) counterparts. Further, pregnant WT and Klf13 null females at Day Postcoitum (DPC) 3.5 had similar uterine Pgr, estrogen receptor, and Wnt-signaling component transcript levels. Nuclear levels of KLF9 were higher in Klf13 null than in WT uteri at DPC 3.5, albeit whole-tissue KLF9 protein and transcript levels did not differ between genotypes. The lack of a similar induction of nuclear KLF9 levels in uteri of virgin Klf13(-/-) mice relative to WT uteri was associated with lower stromal PGR expression. In differentiating human endometrial stromal cells, coincident KLF9/KLF13 knockdown by small interfering RNA targeting reduced decidualization-associated PRL expression, whereas KLF9 and KLF13 knockdowns alone reduced transcript levels of WNT4 and BMP2, respectively. Results suggest that KLF9 and KLF13 functionally compensate in peri-implantation uterus for pregnancy success.
机译:卵巢激素雌激素和孕激素通过其关联受体与上下文依赖性核共调节剂协同作用,促进子宫接受性和成功妊娠。以前,我们表明转录因子Krüppel样因子(KLF)9是子宫中的孕激素受体(PGR)共激活因子,而对Klf9无效的小鼠表现出不育性并降低了孕激素敏感性。高度相关的家庭成员KLF13在怀孕和未怀孕的Klf9 null小鼠的子宫中显示增加的表达,并类似地调节子宫内膜间质细胞中PGR介导的反式激活。但是,尚未报告子宫丢失Klf13的表型。在本研究中,我们证明小鼠Klf13缺乏症不会损害女性的生育能力和妊娠结局。与野生型(WT)雌性相比,Klf13雌性无性仔的产仔数,植入胚胎的数量,子宫形态和卵巢类固醇激素的产生具有可比性。此外,妊娠后天(DP​​C)3.5的孕妇WT和Klf13无效雌性的子宫Pgr,雌激素受体和Wnt信号成分转录水平相似。在DPC 3.5时,Klf13无效的KLF9的核水平高于WT子宫,尽管不同基因型的全组织KLF9蛋白和转录水平没有差异。相对于野生型子宫,在原始Klf13(-/-)小鼠子宫​​中缺乏类似的诱导性核KLF9水平与较低的基质PGR表达相关。在分化人类子宫内膜间质细胞中,靶向小分子干扰RNA的同时发生的KLF9 / KLF13敲除降低了蜕膜化相关的PRL表达,而单独的KLF9和KLF13敲除分别降低了WNT4和BMP2的转录水平。结果表明,KLF9和KLF13在植入前子宫功能上对妊娠成功进行了补偿。

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