Reproductive Medicine Center, Jingmen No.1 People's Hospital, Jingmen, Hubei, China.
Maternity Department, Jingmen No.1 People's Hospital, Jingmen, Hubei, China.
Placenta. 2021 Jan 1;103:156-163. doi: 10.1016/j.placenta.2020.10.023. Epub 2020 Oct 19.
Circ-AK2 has been found to be differentially expressed in PE placenta tissues, however, the role and the underlying molecular mechanisms of circ-AK2 in PE remain poorly known.
The expression of circ-AK2, miR-454-3p, and THBS2 mRNA was detected using quantitative real-time polymerase chain reaction. Protein levels of CyclinD1, MMP-9 and THBS2 were measured using Western blot. Cell proliferation, migration, and invasion were analyzed by 3-(4, 5)-dimethylthiahiazo (-z-y1)-3, 5-di-phenytetrazoliumromide (MTT) assay and transwell assay. The interaction between miR-454-3p and circ-AK2 or THBS2 was analyzed by the dual-luciferase reporter assay.
Circ-AK2 was highly expressed in placental tissues of PE, and overexpression of circ-AK2 inhibited trophoblast cell proliferation, migration and invasion. Circ-AK2 directly bound to miR-454-3p, and miR-454-3p overexpression reversed the inhibitory action of circ-AK2 in biological functions of trophoblast cells. MiR-454-3p was lowly expressed in placental tissues of PE, and directly regulated THBS2 expression in a targeted manner. Silencing miR-454-3p suppressed the proliferating, migratory, and invasive abilities of trophoblast cells, while this condition was abolished by THBS2 knockdown. Besides, we also proved circ-AK2 could regulate THBS2 expression via miR-454-3p.
Circ-AK2 inhibited the proliferation, migration and invasion of trophoblast cells via targeting miR-454-3p/THBS2 axis, suggesting a novel insight into the etiology of PE and a potential therapeutic target for PE treatment.
Circ-AK2 在 PE 胎盘组织中表达差异,但其在 PE 中的作用及潜在分子机制尚不清楚。
采用实时定量聚合酶链反应检测 circ-AK2、miR-454-3p 和 THBS2 mRNA 的表达。采用 Western blot 检测 CyclinD1、MMP-9 和 THBS2 蛋白水平。采用 3-(4,5)-二甲基噻唑 (-z-y1)-3,5-二苯基四氮唑溴盐(MTT)试验和 Transwell 试验分析细胞增殖、迁移和侵袭。通过双荧光素酶报告基因实验分析 miR-454-3p 与 circ-AK2 或 THBS2 的相互作用。
Circ-AK2 在 PE 胎盘组织中高表达,过表达 circ-AK2 抑制滋养细胞增殖、迁移和侵袭。Circ-AK2 直接与 miR-454-3p 结合,miR-454-3p 过表达逆转了 circ-AK2 对滋养细胞生物学功能的抑制作用。miR-454-3p 在 PE 胎盘组织中低表达,直接靶向调节 THBS2 表达。沉默 miR-454-3p 抑制滋养细胞的增殖、迁移和侵袭能力,而 THBS2 敲低则消除了这种情况。此外,我们还证明 circ-AK2 可以通过 miR-454-3p 调节 THBS2 表达。
Circ-AK2 通过靶向 miR-454-3p/THBS2 轴抑制滋养细胞的增殖、迁移和侵袭,为探讨 PE 的病因学提供了新的见解,为治疗 PE 提供了潜在的治疗靶点。