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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >MicroRNA-376c Impairs Transforming Growth Factor-β and Nodal Signaling to Promote Trophoblast Cell Proliferation and InvasionNovelty and Significance
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MicroRNA-376c Impairs Transforming Growth Factor-β and Nodal Signaling to Promote Trophoblast Cell Proliferation and InvasionNovelty and Significance

机译:MicroRNA-376c损害转化生长因子-β和节点信号,促进滋养层细胞增殖和侵袭

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摘要

Preeclampsia is a major disorder of pregnancy and a leading cause of maternal and perinatal morbidity and mortality. MicroRNAs are small noncoding RNAs that regulate gene expression posttranscriptionally. In this study, we examined the expression of miR-376c and found that miR-376c levels were downregulated in both placental and plasma samples collected from preeclamptic patients, when compared with the normal pregnant women at the same gestational stage. Overexpression of miR-376c induced trophoblast cell proliferation, migration, and invasion in HTR8/SVneo cells and promoted placental explant outgrowth. In contrast, inhibition of endogenous miR-376c resulted in a decrease in trophoblast cell invasion and placental explant outgrowth. We identified activin receptor-like kinase 5 (ALK5), a type I receptor for transforming growth factor-β, and ALK7, a type I receptor for Nodal, as targets of miR-376c. Overexpression of miR-376c repressed transforming growth factor-β and Nodal functions, whereas overexpression of ALK5 and ALK7 reversed the effects of miR-376c. These results demonstrate that miR-376c inhibits both ALK5 and ALK7 expression to impair transforming growth factor-β/Nodal signaling, leading to increases in cell proliferation and invasion. An unbalanced Nodal/transforming growth factor-β and miR-376c expression may lead to the development of preeclampsia.
机译:子痫前症是妊娠的主要疾病,是孕产妇和围产儿发病和死亡的主要原因。 MicroRNA是小的非编码RNA,可转录后调控基因表达。在这项研究中,我们检查了miR-376c的表达,发现与同胎妊娠的正常孕妇相比,从先兆子痫患者收集的胎盘和血浆样品中的miR-376c水平均下调。 miR-376c的过表达在HTR8 / SVneo细胞中诱导滋养层细胞增殖,迁移和侵袭,并促进胎盘外植体的生长。相反,抑制内源性miR-376c导致滋养层细胞侵袭和胎盘外植体生长减少。我们确定了激活素受体样激酶5(ALK5)(一种用于转化生长因子-β的I型受体)和ALK7(一种用于Nodal的I型受体)作为miR-376c的靶标。 miR-376c的过表达抑制了转化生长因子-β和Nodal功能,而ALK5和ALK7的过表达逆转了miR-376c的作用。这些结果表明,miR-376c同时抑制ALK5和ALK7表达,从而损害转化生长因子-β/ Nodal信号传导,导致细胞增殖和侵袭增加。节点/转化生长因子-β和miR-376c表达失衡可能导致先兆子痫的发展。

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