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子痫前期miR-4531/CX3CL1信号轴参与血管损伤的体外研究

Effects of miR-4531/CX3CL1 signaling pathway on the vascular injury in preeclampsia in vitro

  • 摘要:
    目的 探讨miR-4531/CX3CL1信号通路在子痫前期血管损伤中的作用,寻找早期诊断和防治子痫前期的潜在靶点。
    方法 选择2021年10月至2022年12月在复旦大学附属闵行医院诊断为晚发型子痫前期的10例患者及同期10例正常妊娠者的胎盘组织样本,用qRT-PCR检测miR-4531和CX3CL1在胎盘组织中的表达水平。通过lipofectamine 2000进行体外细胞转染,用荧光素酶报告基因实验确定miR-4531与CX3CL1之间的结合关系。检测中性粒细胞的凋亡,人脐静脉内皮细胞(HUVECs)的迁移、修复、集落形成、游离DNA(cfDNA)释放等。
    结果 子痫前期患者胎盘组织中miR-4531下调、CX3CL1上调(P<0.05)。荧光素酶报告基因实验显示,miR-4531与CX3CL1之间存在直接结合关系。上调miR-4531促进HUVECs的迁移、增殖和修复,抑制缺氧条件下HUVECs中cfDNA的释放及中性粒细胞的凋亡(P<0.05);下调miR-4531抑制HUVECs的增殖、迁移和修复,增强缺氧条件下HUVECs中cfDNA的释放,促进中性粒细胞的凋亡(P<0.05)。
    结论  子痫前期患者胎盘组织中miR-4531表达下调,可能通过靶向调控CX3CL1通路导致缺氧条件下血管内皮损伤和异常高凝血状态,是PE潜在的治疗靶点。

     

    Abstract:
    Objective To investigate the effects of miR-4531/CX3CL1 signaling pathway on the vascular injury in preeclampsia, and to search possible targets for early diagnosis and prevention of preeclampsia.
    Methods Placental tissue samples were obtained from 10 patients with late-onset preeclampsia and 10 normal pregnant women in the Obstetrics and Gynecology Department of Minhang Hospital, Fudan University from October 2021 to December 2022. The levels of miR-4531 and CX3CL1 were evaluated by qRT-PCR. Cell transfection was performed by lipofectamine 2000 in vitro. The binding relationship between miR-4531 and CX3CL1 was determined by luciferase reporter assay. The apoptosis of neutrophils, the migration, repair, colony formation and cell-free DNA (cfDNA) release of human umbilical vein endothelial cells (HUVECs) were detected.
    Results MiR-4531 was significantly downregulated, and CX3CL1 was upregulated in placental tissues of preeclampsia patients (P<0.05). Luciferase report assay confirmed the direct binding relationship between miR-4531 and CX3CL1. Upregulation of miR-4531significantly promoted the migration, proliferation, repair, and inhibited cfDNA release of HUVECs and neutrophils apoptosis in medium under hypoxic condition (P<0.05). However, downregulation of miR-4531 obviously inhibited the proliferation, migration, repair, and enhanced cfDNA release of HUVECs and neutrophils apoptosis in medium under hypoxic condition (P<0.05).
    Conclusions The miR-4531is downregulated in placental tissues of preeclampsia parients and is a potential therapeutic target for preeclampsia. It might cause endothelial damage and an abnormal hypercoagulable state under hypoxic condition by targeting and regulating the CX3CL1 pathway.

     

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