首页> 外文期刊>Bulletin of experimental biology and medicine >Expression of MicroRNA-146a and MicroRNA-155 in Placental Villi in Early- and Late-Onset Preeclampsia
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Expression of MicroRNA-146a and MicroRNA-155 in Placental Villi in Early- and Late-Onset Preeclampsia

机译:MicroRNA-146A和MicroRNA-155在胎盘绒毛早期和晚期前期前普利坦克斯的表达

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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.
机译:我们在早期或晚期的先兆子痫,我们研究了从18名女性(26-39周)的胎盘绒毛(26-39周)从18名女性(26-39周)中的MicroRNA-146A和MicroRNA-155的表达。参考组由患有生理妊娠和全初期妊娠的妇女,并在妊娠周26-31的剖腹产后的早产。通过用石蜡切片原位杂交检测MicroRNA-146A和MicroRNA-155。结果发现,晚期绒毛血管血管增生的中间绒毛和合胞结的同步性营养细胞中微小RORNA-146a的表达低于全期时期的生理妊娠(P = 0.037和P = 0.001)。早上发病预防患者中间胎盘绒毛绒毛的Syncytootophoblasy的MicroRNA-155的表达高于预递送的基团(P = 0.003)。然而,在中间绒毛的同步性营养细胞和同胞结结中,与全术语生理妊娠相比此外,MicroRNA-146a和microRNA-155的表达在预胰蛋白血症的后期术语中没有增加,而在参考组中,在参考组中表现出随着妊娠年龄的增加,这些标志物的表达逐渐增加。表达MicroRNA-146A和MicroRNA-155在早期和晚期的前普拉姆普拉姆少量不同。这些发现表明,预坦克西亚的不同变体可能是常见的致病途径的特征。受损的滋养细胞不能在所需水平下对MicroRNA合成来维持,这决定了预坦克西亚的恶性循环和疾病的进一步进展。

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