Research Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet.
Faculty of Medicine, University of Oslo.
J Hypertens. 2020 Jul;38(7):1347-1354. doi: 10.1097/HJH.0000000000002362.
Preeclampsia is a syndrome characterized by hypertension and poor placental development. The developmental wingless (Wnt) pathway plays an important role in placental development and we hypothesized that Wnt signaling would be dysregulated in preeclampsia.
To elucidate aberrations in the Wnt signaling pathway we conducted a pathway analysis on placental mRNA in late-onset preeclampsia and normal pregnancy from the STORK study [n = 10 in each group, RNA sequencing (RNAseq)] to identify differentially expressed genes. In addition, we compared circulating levels of secreted Wnt agonists and antagonists at term pregnancy and 6 months postpartum from an acute preeclampsia study (preeclampsia n = 34, normal pregnancy n = 61).
We found circulating and placental mRNA levels of the secreted Wnt agonist R-spondin 3 (RSPO3) at term elevated in preeclampsia. Increased plasma RSPO3 was associated with high mean arterial pressure. Further, pathway analysis of placental tissue revealed elevated mRNA levels of upstream ligands WNT6 and WNT10A and frizzled receptors 2 and 4 in preeclampsia and downstream activation of the noncanonical Ca/NFAT pathway. Finally, plasma dickkopf 3 was decreased in preeclampsia 6 months postpartum.
We identify a potential role for RSPO3 and activation of noncanonical Wnt signaling in preeclampsia.
子痫前期是一种以高血压和胎盘发育不良为特征的综合征。未折叠蛋白(Wnt)通路在胎盘发育中起着重要作用,我们假设 Wnt 信号通路在子痫前期会失调。
为了阐明 Wnt 信号通路的异常,我们对来自 STORK 研究的晚发型子痫前期和正常妊娠的胎盘 mRNA 进行了通路分析(每组 n = 10,RNA 测序(RNAseq)),以鉴定差异表达的基因。此外,我们比较了来自急性子痫前期研究的足月妊娠和产后 6 个月的循环中分泌型 Wnt 激动剂和拮抗剂的水平(子痫前期 n = 34,正常妊娠 n = 61)。
我们发现,子痫前期足月时循环和胎盘 mRNA 水平升高的分泌型 Wnt 激动剂 R 螺旋结构域蛋白 3(RSPO3)。血浆 RSPO3 升高与平均动脉压升高有关。此外,胎盘组织的通路分析显示,子痫前期中上游配体 WNT6 和 WNT10A 以及卷曲受体 2 和 4 的 mRNA 水平升高,非经典 Ca/NFAT 通路的下游激活。最后,子痫前期患者产后 6 个月血浆 Dickkopf 3 降低。
我们确定 RSPO3 和非经典 Wnt 信号通路的激活在子痫前期中可能具有作用。