Department of Obstetrics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, China.
Department of Obstetrics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, China.
Mol Cell Probes. 2019 Apr;44:21-28. doi: 10.1016/j.mcp.2019.01.004. Epub 2019 Jan 24.
Preeclampsia (PE), a special type of hypertensive disorder complicating pregnancy (HDCP), is highly associated with the migratory and invasive capacity of extravillous trophoblasts (EVTs). Here, we aimed to study the functions of low-density lipoprotein receptor-related protein 6 (LRP6) in PE pathogenesis. A comparative analysis of cellular gene expressions between placenta tissues collected from PE patients and normal pregnant women showed that the expressions of LRP6, β-catenin and matrix metallopeptidases/TIMP metallopeptidase inhibitors (MMPs/TIMPs) ratio in placentas of PE patients were much lower than the normal. Then, we constructed and transfected LRP6 siRNA (siLRP6) and LRP6 overexpression vectors into HTR6/SVneo cells. On the contrary to siLRP6, LRP6 overexpression could significant enhance cell viability, and strengthen the abilities of cell migration and invasion. Importantly, the overexpression of LRP6 could induce the upregulation of MMP-2 and MMP-9 levels, and downregulation of TIMPs. The mRNA and protein levels of β-catenin, an intracellular signal transducer of Wnt signaling pathway, were significantly up-regulated under the effects of LRP6 overexpression. XAV939, a Wnt/β-catenin pathway inhibitor, was introduced to confirm the involvement of Wnt/β-catenin pathway in functions of LRP6. The results of cell viability detection showed that XAV939 could significantly inhibit the positive effects of LRP6 overexpression on cell viability. Taken together, low-expressed LRP6 may be responsible of lower migration and invasion of EVTs and subsequent PE, and the mechanisms show a highly association with Wnt/β-catenin pathway.
子痫前期(PE)是一种特殊类型的妊娠高血压疾病(HDCP),与绒毛外滋养细胞(EVTs)的迁移和侵袭能力密切相关。在这里,我们旨在研究低密度脂蛋白受体相关蛋白 6(LRP6)在 PE 发病机制中的作用。对来自 PE 患者和正常孕妇的胎盘组织细胞基因表达的比较分析表明,PE 患者胎盘组织中 LRP6、β-连环蛋白和基质金属蛋白酶/金属蛋白酶抑制剂(MMPs/TIMPs)比值的表达明显低于正常。然后,我们构建并转染 LRP6 siRNA(siLRP6)和 LRP6 过表达载体到 HTR6/SVneo 细胞中。与 siLRP6 相反,LRP6 过表达可以显著增强细胞活力,并增强细胞迁移和侵袭能力。重要的是,LRP6 的过表达可以诱导 MMP-2 和 MMP-9 水平的上调和 TIMPs 的下调。Wnt 信号通路的细胞内信号转导物β-连环蛋白的 mRNA 和蛋白水平在 LRP6 过表达的作用下显著上调。引入 Wnt/β-连环蛋白通路抑制剂 XAV939 来确认 Wnt/β-连环蛋白通路在 LRP6 功能中的参与。细胞活力检测结果表明,XAV939 可显著抑制 LRP6 过表达对细胞活力的正向作用。总之,低表达的 LRP6 可能是 EVTs 迁移和侵袭能力降低以及随后发生 PE 的原因,其机制与 Wnt/β-连环蛋白通路密切相关。