Xu Jingjie, Li Mo, Zhang Lu, Xiong Hao, Lai Lidan, Guo Meijun, Zong Teng, Zhang Dalei, Yang Bei, Wu Lei, Tang Min, Kuang Haibin
Department of Physiology, Nanchang University, Nanchang, Jiangxi, China.
Department of Cell Biology, School of Medicine, Nanchang University, Nanchang, Jiangxi, China.
Mol Reprod Dev. 2015 Nov;82(11):898-906. doi: 10.1002/mrd.22532. Epub 2015 Aug 10.
The androgen receptor (AR) is a ligand-activated transcription factor that is important for both the male and female reproductive systems. The expression and regulation of AR in the uterine endometrium during early pregnancy and decidualization remain relatively under-investigated, so we sought to immunohistochemically examine the spatiotemporal expression of AR in mouse uteri during the peri-implantation period as well as in response to specific steroid hormones. AR protein was found in the nuclei of uterine stromal cells starting on pregnancy Days 1 and 2, with its abundance increasing on Days 3 and 4. From pregnancy Days 5 to 9, however, the expression of AR markedly declined in stromal zones of uteri. No signal was detected in the decidualized cells surrounding the site of embryo implantation; moreover, no AR immunostaining was observed in decidualized uterine cells in an artificial oil-induced model of decidualization. Progesterone significantly inhibited AR protein expression, whereas estrogen dramatically elevated AR abundance in the stroma of ovariectomized mouse uteri. Taken together, our results are the first to demonstrate that decidualization and progesterone significantly inhibited the AR protein expression in vivo, whereas estrogen increased AR protein levels in the stromal cells of mouse uteri. These responses might be advantageous for the proliferation and differentiation of uterine stroma and for embryo implantation during early pregnancy.
雄激素受体(AR)是一种配体激活的转录因子,对男性和女性生殖系统都很重要。在妊娠早期和蜕膜化过程中,子宫内膜中AR的表达和调控仍相对研究不足,因此我们试图通过免疫组织化学方法检测围植入期小鼠子宫中AR的时空表达以及对特定类固醇激素的反应。在妊娠第1天和第2天开始,在子宫基质细胞核中发现了AR蛋白,其丰度在第3天和第4天增加。然而,从妊娠第5天到第9天,子宫基质区AR的表达明显下降。在胚胎植入部位周围的蜕膜化细胞中未检测到信号;此外,在人工油诱导的蜕膜化模型中,蜕膜化的子宫细胞中未观察到AR免疫染色。孕酮显著抑制AR蛋白表达,而雌激素显著提高去卵巢小鼠子宫基质中AR的丰度。综上所述,我们的结果首次证明,蜕膜化和孕酮在体内显著抑制AR蛋白表达,而雌激素增加小鼠子宫基质细胞中AR蛋白水平。这些反应可能有利于妊娠早期子宫基质的增殖和分化以及胚胎植入。