Nizyaeva N V, Kulikova G V, Nagovitsyna M N, Kan N E, Prozorovskaya K N, Shchegolev A I, Sukhikh G T
V. I. Kulakov Research Center for Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation, Moscow, Russia.
Bull Exp Biol Med. 2017 Jul;163(3):394-399. doi: 10.1007/s10517-017-3812-0. Epub 2017 Jul 27.
We studied the expression of microRNA-146a and microRNA-155 in placental villi from 18 women (26-39 weeks of gestation) of reproductive age with early- or late-onset preeclampsia. The reference group consisted of women with physiological pregnancy and full-term gestation and with preterm birth after caesarian section on gestation week 26-31. MicroRNA-146a and microRNA-155 were detected by in situ hybridization with digoxigenin on paraffin sections. It was found that the expression of microRNA-146a in both syncytiotrophoblast of the intermediate villi and syncytial knots was lower at late-onset preeclampsia than at physiologic pregnancy of full-term period (p=0.037 and p=0.001 respectively). The expression of microRNA-155 in syncytiotrophoblast of intermediate placental villi in early-onset preeclampsia was higher than in group with preterm delivery (p=0.003). However, in syncytiotrophoblast of intermediate villi and in syncytial knots, the expression of microRNA-155 was lower at late-onset preeclampsia in comparison with full-term physiological pregnancy (p=0.005). In addition, the expression of microRNA-146a and microRNA-155 did not increase in the later terms in preeclampsia, while in the reference groups demonstrating gradual increase in the expression of these markers with increasing gestational age. Expression microRNA-146a and microRNA-155 little differed in early- and late-onset preeclampsia. These findings suggest that different variants of preeclampsia are probably characterized by common pathogenetic pathways. Damaged trophoblast cannot maintain of microRNAs synthesis at the required level, which determines the formation of a vicious circle in preeclampsia and further progression of the disease.
我们研究了18名育龄期(妊娠26 - 39周)早发型或晚发型子痫前期孕妇胎盘绒毛中微小RNA - 146a和微小RNA - 155的表达情况。对照组由生理妊娠且足月分娩以及在妊娠26 - 31周行剖宫产术后早产的女性组成。通过地高辛原位杂交法在石蜡切片上检测微小RNA - 146a和微小RNA - 155。结果发现,晚发型子痫前期中间绒毛合体滋养层和合体结节中微小RNA - 146a的表达均低于足月生理妊娠(分别为p = 0.037和p = 0.001)。早发型子痫前期胎盘中间绒毛合体滋养层中微小RNA - 155的表达高于早产组(p = 0.003)。然而,与足月生理妊娠相比,晚发型子痫前期中间绒毛合体滋养层和合体结节中微小RNA - 155的表达较低(p = 0.005)。此外,子痫前期晚期微小RNA - 146a和微小RNA - 155的表达并未增加,而在对照组中,随着孕周增加这些标志物的表达逐渐增加。早发型和晚发型子痫前期中微小RNA - 146a和微小RNA - 155的表达差异不大。这些发现表明,不同类型的子痫前期可能具有共同的发病机制。受损的滋养层无法将微小RNA的合成维持在所需水平,这决定了子痫前期恶性循环的形成及疾病的进一步发展。