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白血病抑制因子在胚胎着床及着床腔形成中的时空功能

Spatiotemporal functions of leukemia inhibitory factor in embryo attachment and implantation chamber formation.

作者信息

Aikawa Shizu, Hiraoka Takehiro, Matsuo Mitsunori, Fukui Yamato, Fujita Hidetoshi, Saito-Fujita Tomoko, Shimizu-Hirota Ryoko, Takeda Norihiko, Hiratsuka Daiki, He Xueting, Ishizawa Chihiro, Iida Rei, Akaeda Shun, Harada Miyuki, Wada-Hiraike Osamu, Ikawa Masahito, Osuga Yutaka, Hirota Yasushi

机构信息

Department of Obstetrics and Gynecology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.

出版信息

Cell Death Discov. 2024 Nov 25;10(1):481. doi: 10.1038/s41420-024-02228-4.

Abstract

Embryo implantation is crucial for successful pregnancy, requiring appropriate uterine responses to implantation-competent blastocysts. Molecular communication at the maternal-fetal junction governs this process. Leukemia inhibitory factor (Lif) plays a pivotal role in implantation across species. Lif is abundantly expressed in the glandular epithelium during blastocyst-receptive phase and is induced in the stroma surrounding attached blastocysts. While diminished Lif expression leads to infertility, its influence on peri-implantation uteri remains unclear. Therefore, we investigated the role of Lif in uterine physiology using its uterine-specific knockout (uKO) and uterine epithelial-specific KO (eKO) in mice. Lif eKO and uKO mice displayed infertility owing to failed embryo attachment. Recombinant Lif supplementation rescued the reproductive phenotype of Lif eKO mice, but not Lif uKO mice; however, recombinant Lif injection rescued embryo attachment in Lif uKO mice. RNA-seq analysis indicated that Lif governs uterine epithelial genes, but not embryonic genes, to facilitate embryo attachment via activating nuclear Stat3. Concordantly, three-dimensional imaging of the uterine epithelium revealed that luminal closure and crypt formation are regulated by the uterine Lif-Stat3 axis as well as the presence of blastocysts. Collectively, our findings shed light on previously unknown mechanism on how Lif influences uterine functions molecularly and physiologically during early pregnancy.

摘要

胚胎着床对于成功妊娠至关重要,需要子宫对具备着床能力的囊胚作出适当反应。母胎界面的分子通讯控制着这一过程。白血病抑制因子(Lif)在跨物种着床过程中起关键作用。Lif在囊胚接受期的腺上皮中大量表达,并在附着囊胚周围的基质中被诱导产生。虽然Lif表达降低会导致不孕,但其对围着床期子宫的影响仍不清楚。因此,我们利用小鼠子宫特异性敲除(uKO)和子宫上皮特异性敲除(eKO)来研究Lif在子宫生理中的作用。Lif eKO和uKO小鼠由于胚胎附着失败而表现出不孕。重组Lif补充剂挽救了Lif eKO小鼠的生殖表型,但对Lif uKO小鼠无效;然而,重组Lif注射挽救了Lif uKO小鼠的胚胎附着。RNA测序分析表明,Lif通过激活核Stat3来调控子宫上皮基因而非胚胎基因,以促进胚胎附着。与此一致,子宫上皮的三维成像显示,管腔闭合和隐窝形成受子宫Lif-Stat3轴以及囊胚的存在调控。总的来说,我们的研究结果揭示了Lif在妊娠早期如何在分子和生理水平上影响子宫功能的未知机制。

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