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

IF 6.1 2区 生物学 Q1 CELL BIOLOGY Cell Death Discovery Pub Date : 2024-11-25 DOI:10.1038/s41420-024-02228-4
Shizu Aikawa, Takehiro Hiraoka, Mitsunori Matsuo, Yamato Fukui, Hidetoshi Fujita, Tomoko Saito-Fujita, Ryoko Shimizu-Hirota, Norihiko Takeda, Daiki Hiratsuka, Xueting He, Chihiro Ishizawa, Rei Iida, Shun Akaeda, Miyuki Harada, Osamu Wada-Hiraike, Masahito Ikawa, Yutaka Osuga, Yasushi Hirota
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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.

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白血病抑制因子在胚胎附着和着床室形成中的时空功能
胚胎植入是成功怀孕的关键,需要子宫对具有植入能力的囊胚做出适当的反应。母胎交界处的分子通讯控制着这一过程。白血病抑制因子(Lif)在不同物种的植入过程中发挥着关键作用。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。虽然 Lif 表达减少会导致不孕,但其对着床周围子宫的影响仍不清楚。因此,我们利用小鼠子宫特异性基因敲除(uKO)和子宫上皮特异性基因敲除(eKO)研究了 Lif 在子宫生理中的作用。Lif eKO和uKO小鼠因胚胎附着失败而表现出不孕症。补充重组 Lif 能挽救 Lif eKO 小鼠的生殖表型,但不能挽救 Lif uKO 小鼠的生殖表型;然而,注射重组 Lif 能挽救 Lif uKO 小鼠的胚胎附着。RNA-seq分析表明,Lif通过激活核Stat3来控制子宫上皮基因,而不是胚胎基因,从而促进胚胎附着。同时,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 轴以及囊胚存在的调控。总之,我们的研究结果揭示了 Lif 如何在分子和生理上影响早孕期子宫功能的未知机制。
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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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