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新型基因胚胎植入因子2(EMO2)在小鼠子宫着床部位的表达。

Expression of the novel gene embryo implantation factor 2 (EMO2) in the mouse uterus at the implantation sites.

作者信息

Sun Zhaogui, Su Renwei, Yang Zengming, Shi Huijuan, Liu Chengquan, Wang Jian

机构信息

National Population and Family Planning Committee Key Laboratory of Contraceptives and Devices, Shanghai Institute of Planned Parenthood Research, Shanghai, People's Republic of China.

出版信息

Fertil Steril. 2009 May;91(5 Suppl):2116-22. doi: 10.1016/j.fertnstert.2008.01.092. Epub 2008 Apr 1.

Abstract

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.

摘要

目的

本研究旨在鉴定一种新的与着床相关的分子,并检测围植入期小鼠子宫中EMO2的表达。

设计

实验研究。

地点

研究实验室。

动物

6-8周龄的成年ICR小鼠。

干预措施

成年雌性小鼠与可育雄性小鼠交配以实现妊娠。在第4天对妊娠小鼠进行卵巢切除,并在第5-7天给予孕酮来延迟着床;然后通过给予雌二醇启动着床。通过将雌性小鼠与输精管结扎的雄性小鼠交配获得假孕小鼠。

主要观察指标

通过逆转录-聚合酶链反应检测EMO2 mRNA的组织分布,并通过免疫组织化学确定EMO2蛋白的子宫表达模式。

结果

EMO2的完整cDNA序列已在GenBank中注册(AY372183)。在所有测试的小鼠组织中均观察到EMO2 mRNA表达。在妊娠第5-6天,EMO2蛋白的表达主要定位于着床部位的蜕膜细胞,其表达由活化的胚泡和人工诱导的蜕膜化诱导。

结论

我们的数据表明EMO2可能在小鼠胚胎着床过程中起关键作用。

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