Lalevée S, Lapaire O, Bühler M
Laboratory for Prenatal Medicine, Department of Biomedicine, University Hospital Basel, Basel CH-4031, Switzerland.
1] Laboratory for Prenatal Medicine, Department of Biomedicine, University Hospital Basel, Basel CH-4031, Switzerland [2] Department of Obstetrics and Gynecology, University Hospital Basel, CH-4031 Basel, Switzerland.
Cell Death Dis. 2014 Sep 4;5(9):e1408. doi: 10.1038/cddis.2014.368.
Preeclampsia is a severe pregnancy-related disorder and a leading cause of maternal and fetal mortality worldwide. Early identification of patients with an increased risk for preeclampsia is thus one of the most important goals in obstetrics. Here we identify two related human microRNAs as potential biomarkers to detect at-risk pregnancies. We demonstrate that miR455-3P and miR455-5P are significantly downregulated in placentas from preeclampsia patients, whereas other placenta-specific microRNAs remain unaffected. microRNA target prediction and validation revealed a potential link of miR455-3P to hypoxia signaling. Together with our observation that expression levels of miR455-3P and miR455-5P are upregulated during trophoblast differentiation, our results suggest a model in which miR455-3P represses a hypoxia response that might otherwise prevent cytotrophoblasts from syncytiotrophoblast differentiation. In summary, our work reveals aberrant hypoxia signaling in preeclampsia that can be explained by deregulated expression of miR455. As miR455 has been found in circulating blood, the development of noninvasive prenatal tests enabling early diagnosis of preeclampsia may be possible.
子痫前期是一种严重的妊娠相关疾病,也是全球孕产妇和胎儿死亡的主要原因。因此,早期识别子痫前期风险增加的患者是产科最重要的目标之一。在此,我们鉴定出两种相关的人类微小RNA作为检测高危妊娠的潜在生物标志物。我们证明,子痫前期患者胎盘组织中miR455 - 3P和miR455 - 5P显著下调,而其他胎盘特异性微小RNA不受影响。微小RNA靶标预测和验证揭示了miR455 - 3P与缺氧信号传导之间的潜在联系。结合我们观察到miR455 - 3P和miR455 - 5P在滋养层细胞分化过程中表达上调,我们的结果提示了一种模型,即miR455 - 3P抑制缺氧反应,否则可能阻止细胞滋养层细胞向合体滋养层细胞分化。总之,我们的研究揭示了子痫前期中异常的缺氧信号传导,这可以通过miR455表达失调来解释。由于已在循环血液中发现miR455,开发能够早期诊断子痫前期的非侵入性产前检测可能成为现实。