Department of Physiology & Biophysics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Biol Reprod. 2012 Nov 16;87(5):115. doi: 10.1095/biolreprod.112.102251. Print 2012 Nov.
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.
卵巢激素雌激素和孕激素通过与其同源受体协同作用,并与上下文依赖的核共激活因子一起,促进子宫接受性和成功妊娠。此前,我们表明转录因子 Krüppel 样因子(KLF)9 是子宫中孕激素受体(PGR)的共激活因子,并且 Klf9 缺失的小鼠表现出生育力降低和孕激素敏感性降低。高度相关的家族成员 KLF13 在怀孕和未怀孕的 Klf9 缺失小鼠的子宫中表达增加,并类似地调节子宫内膜基质细胞中 PGR 介导的转录激活。然而,尚未报道 Klf13 缺失的子宫表型。在本研究中,我们证明了小鼠 Klf13 的缺失并不影响雌性生育力和妊娠结局。Klf13 缺失的雌性的产仔数、植入胚胎数、子宫形态和卵巢甾体激素产生与野生型(WT)对照相当。此外,妊娠 WT 和 Klf13 缺失的雌性在妊娠第 3.5 天(DPC)具有相似的子宫 Pgr、雌激素受体和 Wnt 信号成分转录水平。尽管 WT 和 Klf13 缺失的雌性之间的整体组织 KLF9 蛋白和转录水平没有差异,但在 DPC 3.5 时,Klf13 缺失的雌性的核 KLF9 水平高于 WT 子宫。Klf13 缺失的雌性相对于 WT 子宫中核 KLF9 水平的类似诱导缺失与基质 PGR 表达降低有关。在分化的人子宫内膜基质细胞中,通过针对 KLF9/KLF13 的小干扰 RNA 同时敲低会降低蜕膜化相关的 PRL 表达,而单独敲低 KLF9 和 KLF13 会分别降低 WNT4 和 BMP2 的转录水平。结果表明,KLF9 和 KLF13 在着床期子宫中功能上互补,以确保妊娠成功。