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Expression and function of Pdcd4 in mouse endometrium during early pregnancy

机译:妊娠早期小鼠子宫内膜中Pdcd4的表达和功能

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Embryo implantation is a complex process involving synchronised crosstalk between a receptive endometrium and functional blastocysts. Apoptosis plays an important role in this process as well as in the maintenance of pregnancy. In this study, we analysed the expression pattern of programmed cell death 4 ( Pdcd4 ), a gene associated with apoptosis in the mouse endometrium, during early pregnancy and pseudopregnancy by real-time quantitative polymerase chain reaction, in situ hybridisation, Western blotting and immunohistochemistry. The results showed that Pdcd4 was increased along with days of pregnancy and significantly reduced at implantation sites (IS) from day 5 of pregnancy (D5). The level of Pdcd4 at IS was substantially lower than that at interimplantation sites (IIS) on D6 and D7. In addition, Pdcd4 expression in the endometrium was reduced in response to artificially induced decidualisation in vivo and in vitro . Downregulation of Pdcd4 gene expression in cultured primary stromal cells promoted decidualisation, while upregulation inhibited the decidualisation process by increasing apoptosis. These results demonstrate that Pdcd4 is involved in stromal cell decidualisation by mediating apoptosis and therefore plays a role in embryo implantation in mice.
机译:胚胎植入是一个复杂的过程,涉及受孕子宫内膜与功能性胚泡之间的同步串扰。凋亡在该过程以及维持妊娠中起重要作用。在这项研究中,我们通过实时定量聚合酶链反应,原位杂交,Western印迹和免疫组化分析了程序性细胞死亡4(Pdcd4)(一种与小鼠子宫内膜细胞凋亡相关的基因)在早孕和假孕期间的表达模式。 。结果表明,Pdcd4随着怀孕天数的增加而增加,并且从怀孕第5天(D5)起在植入部位(IS)明显减少。 IS上Pdcd4的水平明显低于D6和D7上植入间位点(IIS)的水平。另外,响应于体内和体外人工诱导的蜕膜化,子宫内膜中的Pdcd4表达降低。培养的原代基质细胞中Pdcd4基因表达的下调促进蜕膜形成,而上调则通过增加凋亡来抑制蜕膜形成过程。这些结果表明Pdcd4通过介导凋亡参与基质细胞蜕膜化,因此在小鼠胚胎植入中起作用。

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