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雌激素通过 CCAAT/增强子结合蛋白-β在胚胎着床和蜕膜化期间调节小鼠子宫中的阿米洛利结合蛋白 1。

Estrogen regulates amiloride-binding protein 1 through CCAAT/enhancer-binding protein-beta in mouse uterus during embryo implantation and decidualization.

机构信息

Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, School of Life Science, Xiamen University, Xiamen 361005, China.

出版信息

Endocrinology. 2010 Oct;151(10):5007-16. doi: 10.1210/en.2010-0170. Epub 2010 Jul 28.

Abstract

Embryo implantation is an intricate interaction between receptive uterus and active blastocyst. The mechanism underlying embryo implantation is still unknown. Although histamine and putrescine are important for embryo implantation and decidualization, excess amount of histamine and putrescine is harmful. Amiloride binding protein 1 (Abp1) is a membrane-associated amine oxidase and mainly metabolizes histamine and putrescine. In this study, we first showed that Abp1 is strongly expressed in the decidua on d 5-8 of pregnancy. Abp1 expression is not detected during pseudopregnancy and under delayed implantation but is detected after estrogen activation. Because Abp1 is mainly localized in the decidua and also strongly expressed during in vitro decidualization, Abp1 might play a role during mouse decidualization. The regulation of estrogen on Abp1 is mediated by transcription factor CCAAT/enhancer-binding protein-β. Abp1 expression is also regulated by cAMP, bone morphogenetic protein 2, and ERK1/2. Abp1 may be essential for mouse embryo implantation and decidualization.

摘要

胚胎着床是一个复杂的过程,涉及到接受性子宫和活跃的囊胚之间的相互作用。胚胎着床的机制尚不清楚。虽然组胺和腐胺对于胚胎着床和蜕膜化很重要,但过量的组胺和腐胺是有害的。胺氧化酶结合蛋白 1(Abp1)是一种膜相关的胺氧化酶,主要代谢组胺和腐胺。在本研究中,我们首先表明 Abp1 在妊娠第 5-8 天的蜕膜中强烈表达。在假孕和延迟着床期间未检测到 Abp1 的表达,但在雌激素激活后检测到。由于 Abp1 主要定位于蜕膜中,并且在体外蜕膜化过程中也强烈表达,因此 Abp1 可能在小鼠蜕膜化过程中发挥作用。雌激素对 Abp1 的调节是通过转录因子 CCAAT/增强子结合蛋白-β介导的。Abp1 的表达还受到 cAMP、骨形态发生蛋白 2 和 ERK1/2 的调节。Abp1 可能对于小鼠胚胎着床和蜕膜化是必需的。

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