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Characterization of IK cytokine expression in mouse endometrium during early pregnancy and its significance on implantation

机译:妊娠早期小鼠子宫内膜中IK细胞因子表达的表征及其对植入的意义

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The expression of IK?cytokine was investigated in the mouse endometrium during early pregnancy (D1-D7 of pregnancy) and pseudopregnancy using real-time PCR, western blotting and immunohistochemical analysis, and the effects of IK?cytokine on embryo implantation were observed by injection with antisense IK?cytokine oligodeoxynucleotides in the uterine horn. Our data showed that the expression of IK?cytokine mRNA increased gradually from D1 to D4 of pregnancy and reached a peak level at D4 of pregnancy (P<0.05). Western blotting and immunohistochemical analysis revealed that the expression of IK?cytokine protein increased gradually from D1 to D5 of pregnancy and reached a peak level at D5 of pregnancy (P<0.05). The expression of IK?cytokine in the pseudopregnant uterus was significantly lower compared to that in the normal pregnant uterus and the level of the protein never showed a high peak during the whole pseudopregnancy. The expression of IK?cytokine at the implantation site was much stronger than that in the peri-implantation site on Day?5 of pregnancy. After 24 and 48?h of injection with antisense IK?cytokine oligodexynucleotides in the uterine horn on D3 of pregnancy (i.e. implantation window), the expression of IK?cytokine in the uterus was remarkably inhibited, while the expression of major histocompatibility complex?Ⅱ (MHCⅡ) increased and the number of implanted embryos significantly decreased in the site of uterine horns receiving antisense IK?cytokine (P<0.05). These results suggested that IK?cytokine may play a crucial role in implantation.
机译:采用实时荧光定量PCR,免疫印迹和免疫组化分析方法,研究了妊娠早期(妊娠D1-D7)和假孕小鼠子宫内膜中IK?细胞因子的表达,并观察了IK?细胞因子对胚胎植入的影响。在子宫角中含有反义IK?细胞因子寡聚脱氧核苷酸。我们的数据显示,IK?细胞因子mRNA的表达从妊娠的D1到D4逐渐增加,并在妊娠的D4达到峰值(P <0.05)。 Western blotting和免疫组织化学分析显示,IK?细胞因子蛋白的表达从妊娠D1到D5逐渐增加,并在妊娠D5达到峰值(P <0.05)。与假孕子宫相比,假孕子宫中IK?细胞因子的表达明显降低,并且蛋白质水平在整个假孕期间从未显示出高峰值。妊娠第5天,IK?细胞因子在植入部位的表达要强于植入周缘部位。在妊娠第3天(即植入窗口)子宫角注射反义IK?细胞因子寡聚核苷酸后24小时和48?h,子宫内IK?细胞因子的表达受到明显抑制,而主要组织相容性复合物的表达Ⅱ反义IK细胞因子在子宫角部位(MHCⅡ)增加(MHCⅡ),植入的胚胎数目明显减少(P <0.05)。这些结果表明IK细胞因子可能在植入中起关键作用。

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