Zhou Yi, Xu Qiu Lian
Department of Obstetrics, Jinhua People's Hospital, 267 Danxi East Road, Jindong District, Jinhua, 321000, China.
Sci Rep. 2025 May 7;15(1):15861. doi: 10.1038/s41598-025-00249-2.
To explore the molecular mechanism of miRNA-155-5p regulating placental trophoblast cell function and affecting preeclampsia. RNA was measured via RT-qPCR, and protein was detected with Western blot as well as Immunohistochemistry. Cell viability, proliferation, migration as well as invasion were detected via CCK8 assay, EDU stain as well as Transwell. Tunel assay measures cell apoptosis. Dual-Luciferase Reporter Assay affirms targeting relationships of miRNA-155-5p and PIK3R1. MiR-155-5p in PE patients' placental trophoblasts was markedly higher, while PIK3R1 was lower. Knockdown of miR-155-5p in trophoblast enhanced cell viability, proliferation, migration as well as invasion, while reducing apoptosis. The predicted target gene of miR-155-5p was PIK3R1, while PIK3R1 expression was inversely correlated to miR-155-5p in HTR-8/SVneo. In trophoblast overexpressing miR-155-5p, increased PIK3R1 expression could reverse the effect. We confirmed that miR-155-5p affects the function of placental trophoblast HTR-8/SVneo, and confirmed that miR-155-5p affects the development of PE by regulating PIK3R1, which provides a target for treatment as well as prevention of PE.
探索miRNA-155-5p调控胎盘滋养层细胞功能及影响子痫前期的分子机制。通过RT-qPCR检测RNA,采用蛋白质免疫印迹法及免疫组织化学法检测蛋白质。通过CCK8检测、EDU染色及Transwell检测细胞活力、增殖、迁移及侵袭。Tunel检测法测定细胞凋亡。双荧光素酶报告基因检测法确认miRNA-155-5p与PIK3R1的靶向关系。子痫前期患者胎盘滋养层细胞中miR-155-5p明显升高,而PIK3R1降低。在滋养层细胞中敲低miR-155-5p可增强细胞活力、增殖、迁移及侵袭,同时减少细胞凋亡。miR-155-5p的预测靶基因是PIK3R1,在HTR-8/SVneo中PIK3R1表达与miR-155-5p呈负相关。在过表达miR-155-5p的滋养层细胞中,增加PIK3R1表达可逆转该效应。我们证实miR-155-5p影响胎盘滋养层细胞HTR-8/SVneo的功能,并证实miR-155-5p通过调控PIK3R1影响子痫前期的发生发展,这为子痫前期的治疗及预防提供了靶点。