微小 RNA-454 通过调节 Eph 受体 B4 的表达,参与调节子痫前期滋养细胞的增殖、凋亡和侵袭。

MicroRNA-454 is involved in regulating trophoblast cell proliferation, apoptosis, and invasion in preeclampsia by modulating the expression of ephrin receptor B4.

机构信息

Department of Obstetrics, Affiliated Hospital of Shaanxi University of Chinese Medicine, Xianyang, Shaanxi 712046, China.

Shaanxi University of Chinese Medicine, Xianyang, Shaanxi 712046, China.

出版信息

Biomed Pharmacother. 2018 Nov;107:746-753. doi: 10.1016/j.biopha.2018.08.055. Epub 2018 Aug 20.

Abstract

Preeclampsia (PE) is a pregnancy-specific disorder representing a major cause for maternal and perinatal morbidity and mortality. The dysfunction of trophoblast cells plays an important role in the pathogenesis of PE. In recent years, microRNAs (miRNAs) have been suggested to play an important role in regulating trophoblast cell biological functions involved in the pathogenesis of PE. Accumulating evidence has showed that miR-454 plays an important role in regulating cell functions. However, whether miR-454 is involved in regulating cell functions of trophoblast cells during PE remains unclear. In this study, we found that miR-454 expression was significantly downregulated in placental tissues from PE patients. in vitro experiments showed that miR-454 overexpression significantly increased proliferation, inhibited apoptosis, and promoted invasion of trophoblast cells, whereas miR-454 inhibition markedly suppressed proliferation, increased apoptosis, and inhibited invasion of trophoblast cells. Interestingly, bioinformatics analysis predicted that ephrin receptor B4 (EPHB4), an important gene for regulating trophoblast cell function in PE, was a potential target gene of miR-454. Dual-luciferase reporter assay showed that miR-454 directly targeted the 3'-untranslated region of EPHB4. Real-time quantitative polymerase chain reaction and Western blot analysis demonstrated that miR-454 negatively regulated EPHB4 expression in trophoblast cells. Moreover, miR-454 expression was found inversely correlated with EPHB4 expression in placental tissues from PE patients. Importantly, EPHB4 overexpression partially reversed the promotion effect of miR-454 overexpression on trophoblast cell proliferation and invasion. Taken together, these findings demonstrate that miR-454 promotes the proliferation and invasion of trophoblast cells by inhibiting EPHB4 expression, and the decreased miR-454 expression may contribute to PE by promoting EPHB4 expression. Our study provides novel insights into understanding the molecular pathogenesis of PE.

摘要

子痫前期(PE)是一种妊娠特有的疾病,是孕产妇和围产儿发病率和死亡率的主要原因。滋养细胞功能障碍在 PE 的发病机制中起着重要作用。近年来,microRNAs(miRNAs)被认为在调节与 PE 发病机制相关的滋养细胞生物学功能中起着重要作用。越来越多的证据表明,miR-454 在调节细胞功能中起着重要作用。然而,miR-454 是否参与调节 PE 期间滋养细胞的细胞功能仍不清楚。在这项研究中,我们发现 miR-454 在 PE 患者的胎盘组织中的表达明显下调。体外实验表明,miR-454 的过表达显著增加了滋养细胞的增殖,抑制了凋亡,并促进了侵袭,而 miR-454 的抑制则显著抑制了增殖,增加了凋亡,并抑制了滋养细胞的侵袭。有趣的是,生物信息学分析预测,Ephrin 受体 B4(EPHB4)是调节 PE 中滋养细胞功能的重要基因,是 miR-454 的一个潜在靶基因。双荧光素酶报告基因检测显示,miR-454 直接靶向 EPHB4 的 3'-非翻译区。实时定量聚合酶链反应和 Western blot 分析表明,miR-454 负调控滋养细胞中 EPHB4 的表达。此外,在 PE 患者的胎盘组织中发现 miR-454 的表达与 EPHB4 的表达呈负相关。重要的是,EPHB4 的过表达部分逆转了 miR-454 过表达对滋养细胞增殖和侵袭的促进作用。总之,这些发现表明,miR-454 通过抑制 EPHB4 的表达促进滋养细胞的增殖和侵袭,而 miR-454 表达的降低可能通过促进 EPHB4 的表达导致 PE。我们的研究为理解 PE 的分子发病机制提供了新的见解。

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