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Uterine NDRG2 expression is increased at implantation sites during early pregnancy in mice, and its down-regulation inhibits decidualization of mouse endometrial stromal cells

机译:小鼠妊娠早期子宫NDRG2表达在植入部位增加,其下调抑制小鼠子宫内膜基质细胞的蜕膜化

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Background N-myc down-regulated gene 2 (NDRG2) is a tumor suppressor involved in cell proliferation and differentiation. The aim of this study was to determine the uterine expression pattern of this gene during early pregnancy in mice. Methods Uterine NDRG2 mRNA and protein expression levels were determined by RT-PCR and Western blot analyses, respectively, during the peri-implantation period in mice. Immunohistochemical (IHC) analysis was performed to examine the spatial localization of NDRG2 expression in mouse uterine tissues. The in vitro decidualization model of mouse endometrial stromal cells (ESCs) was used to evaluate decidualization of ESCs following NDRG2 knock down by small interfering RNA (siRNA). Statistical significance was analyzed by one-way ANOVA using SPSS 19.0 software. Results Uterine NDRG2 gene expression was significantly up-regulated and was predominantly localized to the secondary decidual zone on days 5 and 8 of pregnancy in mice. Its increased expression was associated with artificial decidualization as well as the activation of delayed implantation. Furthermore, uterine NDRG2 expression was induced by estrogen and progesterone treatments. The in vitro decidualization of mouse ESCs was accompanied by up-regulation of NDRG2 expression, and knock down of its expression in these cells by siRNA inhibited the decidualization process. Conclusions These results suggest that NDRG2 might play an important role in the process of decidualization during early pregnancy.
机译:背景N-myc下调基因2(NDRG2)是一种肿瘤抑制因子,参与细胞增殖和分化。这项研究的目的是确定小鼠早期妊娠期间该基因的子宫表达模式。方法采用RT-PCR和Western blot方法分别测定围着床期小鼠子宫内NDRG2的mRNA和蛋白表达水平。进行了免疫组织化学(IHC)分析,以检测小鼠子宫组织中NDRG2表达的空间定位。小鼠子宫内膜基质细胞(ESCs)的体外蜕膜化模型用于评估NDRG2被小干扰RNA(siRNA)敲除后的ESC蜕膜化。使用SPSS 19.0软件通过单因素方差分析分析统计学显着性。结果小鼠NDRG2基因表达在小鼠妊娠的第5天和第8天显着上调,并主要位于次蜕膜区。其增加的表达与人工蜕膜化以及延迟植入的激活有关。此外,子宫NDRG2表达是由雌激素和孕激素治疗诱导的。小鼠ESC的体外蜕膜化伴随NDRG2表达的上调,而siRNA抑制这些细胞中NDRG2表达的表达抑制了蜕膜化过程。结论这些结果表明,NDRG2可能在妊娠早期的蜕膜化过程中起重要作用。

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