Department of Obstetrics, The Second Hospital of Hebei Medical University, No. 215 Heping Xi Road, Shijiazhuang, 050000, Hebei, China.
Hum Cell. 2020 Jul;33(3):512-520. doi: 10.1007/s13577-020-00322-0. Epub 2020 Mar 4.
Pre-eclampsia (PE) is a disorder of pregnancy characterized by proteinuria and high blood pressure, affecting 2-8% of pregnancies worldwide. Previous studies have shown that PE is closely associated with trophoblast cell dysfunction. Here, we investigated the role of tissue factor pathway inhibitor-2 (TFPI-2) in regulating the biological processes of trophoblast cells. The TFPI-2 levels in plasma samples and placental tissues were tested by ELISA, immunohistochemistry, qRT-PCR, and western blot. HTR8/Svneo cell line was used to simulate the primary trophoblast cells and H/R culture was applied to mimic the oxidative stress state of PE. MTT assay, Annexin V/propidium iodide (PI) apoptosis assay, and transwell assay were used to determine the cell proliferation, apoptosis, and invasion. The expression levels of matrix metalloproteinases (MMPs) were evaluated by western blot. The expression of TFPI-2 was remarkably up-regulated in both the serum and placenta of PE patients. Hypoxia/reoxygenation increased the expression of TFPI-2 in HTR-8/SVneo cell line. TFPI-2 promoted that cell proliferation and inhibited the cell apoptosis of HTR8/SVneo cells in H/R condition. In addition, downregulation of TFPI-2 increased the cell invasion and the expression of MMP2 and MMP9. This study reveals that TFPI-2 plays a crucial role in monitoring the biological function of trophoblast cells, which might provide theoretical basis and therapeutic targets for the treatment of PE.
子痫前期(PE)是一种妊娠并发症,以蛋白尿和高血压为特征,影响全球 2-8%的妊娠。先前的研究表明,PE 与滋养细胞功能障碍密切相关。在这里,我们研究了组织因子途径抑制剂-2(TFPI-2)在调节滋养细胞生物学过程中的作用。通过 ELISA、免疫组织化学、qRT-PCR 和 Western blot 检测血浆样本和胎盘组织中的 TFPI-2 水平。使用 HTR8/Svneo 细胞系模拟原发性滋养细胞,并应用 H/R 培养模拟 PE 的氧化应激状态。MTT 测定、Annexin V/碘化丙啶(PI)凋亡测定和 Transwell 测定用于确定细胞增殖、凋亡和侵袭。通过 Western blot 评估基质金属蛋白酶(MMPs)的表达水平。PE 患者的血清和胎盘均显著上调 TFPI-2 的表达。缺氧/复氧增加 HTR-8/SVneo 细胞系中 TFPI-2 的表达。TFPI-2 在 H/R 条件下促进 HTR8/SVneo 细胞的增殖并抑制细胞凋亡。此外,下调 TFPI-2 增加了细胞侵袭和 MMP2 和 MMP9 的表达。本研究揭示 TFPI-2 在监测滋养细胞生物学功能方面起着至关重要的作用,这可能为 PE 的治疗提供理论基础和治疗靶点。