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首页> 外文期刊>EBioMedicine >poFUT1 promotes endometrial decidualization by enhancing the O-fucosylation of Notch1
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poFUT1 promotes endometrial decidualization by enhancing the O-fucosylation of Notch1

机译:poFUT1通过增强Notch1的O-岩藻糖基化来促进子宫内膜蜕膜化

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Background Endometrial stromal cell decidualization is critical for embryo implantation. Dysfunctional decidualization leads to implantation failure, miscarriage and even pregnancy associated disorders in subsequent pregnancy trimesters. Protein glycosylation is involved in many physiological and pathological processes. Protein O-fucosyltransferase 1 (poFUT1) is the key enzyme for the O-fucosylation of proteins. However, the role and mechanism of poFUT1 in human endometrial stromal cell decidualization remain elusive. Methods We employed immunohistochemistry to detect the level of poFUT1 in the uterine endometrium from those of the proliferative phase, secretory phase, early pregnancy women and miscarriage patients. Using human endometrial stromal cells (hESCs) and a mouse model, the underlying mechanisms of poFUT1 in decidualization was investigated. Findings The level of poFUT1 was increased in the stromal cells of the secretory phase relative to those in the proliferative phase of the menstrual cycle, and decreased in the stromal cells of miscarriage patients compared to women with healthy early pregnancies. Furthermore, we found that poFUT1 promoted hESCs decidualization. The results also demonstrated that poFUT1 increased O-fucosylation on Notch1 in hESCs, which activated Notch1 signaling pathway. Activated Notch1 (NICD), as a specific trans-factor of PRL and IGFBP1 promoters, enhanced PRL and IGFBP1 transcriptional activity, thus inducing hESCs decidualization. Interpretation Level of poFUT1 is lower in the uterine endometrium from miscarriage patients than early pregnancy women. poFUT1 is critical in endometrial decidualization by controlling the O-fucosylation on Notch1. Our findings provide a new mechanism perspective on poFUT1 in uterine decidualization that may be a useful diagnostic and therapeutic target for miscarriage. Fund National Natural Science Foundation of China (31770857, 31670810 and 31870794). Liaoning Provincial Program for Top Discipline of Basic Medical Sciences.
机译:背景子宫内膜基质细胞蜕膜化对于胚胎植入至关重要。蜕膜功能异常导致随后的妊娠中期植入失败,流产,甚至导致妊娠相关疾病。蛋白糖基化涉及许多生理和病理过程。蛋白质O-岩藻糖基转移酶1(poFUT1)是蛋白质O-岩藻糖基化的关键酶。但是,poFUT1在人子宫内膜基质细胞蜕膜化中的作用和机制仍然难以捉摸。方法采用免疫组织化学方法检测增生期,分泌期,早孕妇女和流产患者子宫内膜中poFUT1的水平。使用人类子宫内膜基质细胞(hESCs)和小鼠模型,研究了蜕膜化过程中poFUT1的潜在机制。结果与健康早孕妇女相比,分泌期基质细胞中poFUT1的水平相对于月经周期增生阶段中的升高,而流产患者基质细胞中的降低。此外,我们发现poFUT1促进hESC蜕膜化。结果还表明,poFUT1增加了hESCs中Notch1的O-岩藻糖基化,从而激活了Notch1信号通路。激活的Notch1(NICD),作为PRL和IGFBP1启动子的特定反式因子,可以增强PRL和IGFBP1的转录活性,从而诱导hESC蜕膜化。流产患者子宫内膜中poFUT1的解释水平低于早孕妇女。通过控制Notch1的O-岩藻糖基化,poFUT1在子宫内膜蜕膜化中至关重要。我们的发现为子宫蜕膜化中poFUT1的新机制提供了视角,这可能是流产的有用诊断和治疗目标。获国家自然科学基金资助(31770857、31670810和31870794)。辽宁省基础医学优秀学科计划。

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