Tianjin Key Laboratory of human development and reproductive regulation, Tianjin Central Hospital of Gynecology Obstetrics, No. 156 Nankai Sanma Road Nankai District, Tianjin, 300100, China.
Tianjin Key Laboratory of human development and reproductive regulation, Tianjin Central Hospital of Gynecology Obstetrics, No. 156 Nankai Sanma Road Nankai District, Tianjin, 300100, China.
Transpl Immunol. 2022 Oct;74:101666. doi: 10.1016/j.trim.2022.101666. Epub 2022 Jul 6.
Preeclampsia (PE) is a syndrome commonly occurring among the pregnant. Shallow trophoblast invasion is considered to be closely related to PE. Therefore, in trophoblast cells, we explored the potential mechanisms of lncRNA XIST in the modulation of trophoblast invasion and proliferation.
GEO online analyzer was used to screen the abnormally expressed RNAs in placenta tissues from patients with severe PE and healthy controls. The prediction of target bindings was performed on TargetScan and starBase. Transfection was conducted to regulate the RNA expression levels in trophoblast cells, HTR-8/SVneo. RT-qPCR measured expression of lncRNA XIST, miR-340-5p and KCNJ16. The CCK-8 assay examined cell viability. Flow cytometer analyzed apoptosis and luciferase assay determined the luciferase activity. Transwell assays detected the invasion and western blot verified the changes in protein expression of MMP2, MMP9 and KCNJ16 in trophoblast cells.
lncRNA XIST expression was enhanced in PE patients. Upregulation of lncRNA XIST in HTR-8/SVneo cells inhibited the cell proliferation and invasion, and induced apoptosis. XIST upregulation inhibited MMP2 and MMP9 protein expression. lncRNA XIST/ KCNJ16 interplayed as ceRNAs of miR-340-5p. Specifically,miR-340-5p overexpression reversed the effect of XIST upregulation on the cell apoptosis, proliferation and invasive ability and the knockdown of KCNJ16 could add to the effect of miR-340-5p overexpression in HTR-8/SVneo.
lncRNA XIST was upregulated in PE. Upregulation of lncRNA XIST exerted the inhibitory effects on the proliferation and invasion of trophoblast cells through the interactions with miR-340-5p/KCNJ16, which suggests that the lncRNA XIST/miR-340-5p/KCNJ16 axis might play a role in PE.
子痫前期(PE)是孕妇中常见的综合征。浅绒毛浸润被认为与 PE 密切相关。因此,在滋养细胞中,我们探索了长链非编码 RNA XIST 在调节滋养细胞侵袭和增殖中的潜在机制。
使用 GEO 在线分析器筛选来自重度 PE 患者和健康对照者胎盘组织中异常表达的 RNA。使用 TargetScan 和 starBase 进行靶基因结合预测。转染调节滋养细胞 HTR-8/SVneo 中的 RNA 表达水平。RT-qPCR 检测 lncRNA XIST、miR-340-5p 和 KCNJ16 的表达。CCK-8 测定细胞活力。流式细胞仪分析细胞凋亡,荧光素酶测定检测荧光素酶活性。Transwell 检测侵袭,Western blot 检测滋养细胞中 MMP2、MMP9 和 KCNJ16 蛋白表达的变化。
PE 患者中 lncRNA XIST 的表达增强。HTR-8/SVneo 细胞中 lncRNA XIST 的上调抑制细胞增殖和侵袭,并诱导细胞凋亡。XIST 上调抑制 MMP2 和 MMP9 蛋白表达。lncRNA XIST/KCNJ16 作为 miR-340-5p 的 ceRNA 相互作用。具体来说,miR-340-5p 的过表达逆转了 XIST 上调对细胞凋亡、增殖和侵袭能力的影响,而 KCNJ16 的敲低可以增强 miR-340-5p 过表达在 HTR-8/SVneo 中的作用。
PE 中 lncRNA XIST 上调。lncRNA XIST 的上调通过与 miR-340-5p/KCNJ16 的相互作用,对滋养细胞的增殖和侵袭发挥抑制作用,提示 lncRNA XIST/miR-340-5p/KCNJ16 轴可能在 PE 中发挥作用。