Jiashuo Zhang, Lan Mei, Yanping Zhang, Xiaohong Wei, Min Liu, Yangxue Yin, Qin Xu, Lingyun Liao, Linbo Gao, Rong Zhou
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Poly(A)-binding protein cytoplasmic 1 (PABPC1) was a target protein of lncRNA-ATB, and its expression was positively regulated by lncRNA-ATB in trophoblasts. Reduced PABPC1 expression inhibited proliferation, migration, invasion, and tube formation, and enhanced apoptosis in trophoblast cells. In sPE-affected placentas, PABPC1 expression was reduced, which may have mediated the effect of lncRNA-ATB on MDM2. Moreover, MDM2 expression was inhibited after lncRNA-ATB or PABPC1 knockdown in trophoblasts, and reduced MDM2 expression suppressed trophoblast biological functions. Further, the interaction between PABPC1 and MDM2 was suggested to be mediated by p53, and p53 expression was negatively regulated by PABPC1. In summary, PABPC1 mediates the effects of lncRNA-ATB on trophoblast biological functions via the p53/MDM2 pathway. 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引用次数: 0
摘要
异常螺旋状动脉重构是子痫前期的起点。重度子痫前期(sPE)患者胎盘lncRNA-ATB水平显著降低,这些水平降低可抑制HTR-8/SVneo滋养细胞的生物学功能。然而,lncRNA-ATB调控滋养层细胞生物学行为的机制尚不清楚。在这里,我们旨在鉴定滋养细胞中与lncRNA-ATB相互作用的蛋白,并揭示与该分子相关的生物学调控机制。本研究采用RNA-protein pull-down和RNA免疫沉淀法鉴定lncRNA-ATB下游因子。Poly(A)-binding protein cytoplasmic 1 (PABPC1)是lncRNA-ATB的靶蛋白,其在滋养细胞中的表达受到lncRNA-ATB的正调控。减少PABPC1表达抑制滋养细胞的增殖、迁移、侵袭和管形成,并增强细胞凋亡。在spe影响的胎盘中,PABPC1表达降低,这可能介导了lncRNA-ATB对MDM2的影响。此外,lncRNA-ATB或PABPC1敲低滋养层细胞后,MDM2表达受到抑制,MDM2表达降低抑制滋养层细胞生物学功能。此外,PABPC1与MDM2的相互作用可能是由p53介导的,并且PABPC1负向调节p53的表达。综上所述,PABPC1通过p53/MDM2通路介导lncRNA-ATB对滋养细胞生物学功能的影响。我们的发现为lncRNA-ATB在sPE发病机制中的作用提供了新的视角。
LncRNA-ATB Contributes to Severe Preeclampsia by Modulating the p53/MDM2 Pathway via PABPC1
Abnormal spiral artery remodeling is the starting point of preeclampsia. Placental lncRNA-ATB levels are significantly reduced in patients with severe preeclampsia (sPE), and these reduced levels can inhibit the biological functions of HTR-8/SVneo trophoblasts. However, the mechanism by which lncRNA-ATB regulates the biological behavior of trophoblasts remains unclear. Here, we aimed to identify proteins that interact with lncRNA-ATB in trophoblasts and uncover the biological regulatory mechanism associated with this molecule. In this study, RNA-protein pull-down and RNA immunoprecipitation tests were used to identify lncRNA-ATB downstream factors. Poly(A)-binding protein cytoplasmic 1 (PABPC1) was a target protein of lncRNA-ATB, and its expression was positively regulated by lncRNA-ATB in trophoblasts. Reduced PABPC1 expression inhibited proliferation, migration, invasion, and tube formation, and enhanced apoptosis in trophoblast cells. In sPE-affected placentas, PABPC1 expression was reduced, which may have mediated the effect of lncRNA-ATB on MDM2. Moreover, MDM2 expression was inhibited after lncRNA-ATB or PABPC1 knockdown in trophoblasts, and reduced MDM2 expression suppressed trophoblast biological functions. Further, the interaction between PABPC1 and MDM2 was suggested to be mediated by p53, and p53 expression was negatively regulated by PABPC1. In summary, PABPC1 mediates the effects of lncRNA-ATB on trophoblast biological functions via the p53/MDM2 pathway. Our findings provide a new perspective on the role of lncRNA-ATB in sPE pathogenesis.
期刊介绍:
The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.