首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Expression of the novel gene embryo implantation factor 2 (EMO2) in the mouse uterus at the implantation sites.
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Expression of the novel gene embryo implantation factor 2 (EMO2) in the mouse uterus at the implantation sites.

机译:新基因胚胎植入因子2(EMO2)在小鼠子宫中植入部位的表达。

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摘要

OBJECTIVE: The aim of this study was to identify a novel implantation-related molecule and to examine EMO2 expression in the mouse uterus during the peri-implantation period. DESIGN: Experimental study. SETTING: Research laboratory. ANIMAL(S): Adult ICR mice aged 6-8 weeks. INTERVENTION(S): Adult female mice were mated with fertile males to achieve pregnancy. Implantation was delayed by ovariectomizing pregnant mice on day 4 and administering P during days 5-7; implantation was then initiated by administering E(2). Pseudopregnant mice were obtained by mating females with vasectomized males. MAIN OUTCOME MEASURE(S): The tissue distribution of EMO2 mRNA was detected by reverse transcriptase-polymerase chain reaction, and the uterine expression pattern of the EMO2 protein was determined by immunohistochemistry. RESULT(S): The full cDNA sequence of EMO2 was registered in GenBank (AY372183). EMO2 mRNA expression was observed in all mouse tissues tested. The expression of the EMO2 protein was predominately localized in decidual cells at the implantation site during days 5-6 of pregnancy, and its expression was induced by the active blastocyst and artificially induced decidualization. CONCLUSION(S): Our data indicate that EMO2 may play a key role in the mouse embryo implantation process.
机译:目的:本研究的目的是鉴定一种新的与植入有关的分子,并检查植入前后围着小鼠子宫中EMO2的表达。设计:实验研究。地点:研究实验室。动物:6-8周大的成年ICR小鼠。干预:成年雌性小鼠与可育雄性动物交配以怀孕。通过在第4天去卵巢妊娠小鼠并在第5-7天给予P来延迟植入。然后通过管理E(2)开始植入。通过将雌性与切除阴茎的雄性交配获得假孕小鼠。主要观察指标:通过逆转录酶-聚合酶链反应检测EMO2 mRNA的组织分布,并通过免疫组化方法检测EMO2蛋白的子宫表达模式。结果:EMO2的完整cDNA序列已在GenBank(AY372183)中进行了注册。在所有测试的小鼠组织中均观察到EMO2 mRNA表达。 EMO2蛋白的表达主要在妊娠的5-6天期间位于植入部位的蜕膜细胞中,并且其表达是由活跃的胚泡和人工诱导的蜕膜化诱导的。结论:我们的数据表明EMO2可能在小鼠胚胎植入过程中起关键作用。

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