ACVR2A 在子痫前期进展中通过 TCF7/c-JUN 通路促进滋养层细胞侵袭

Shujing Yang, Huanyao Liu, Jieshi Hu, Bingjun Chen, Wanlu An, Xuwen Song, Yi Yang, Fang He
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引用次数: 0

摘要

子痫前期(PE)是一种与遗传因素有关的严重妊娠疾病,尤其是 ACVR2A 基因,该基因编码的受体参与活化素信号通路,在生殖过程中发挥关键作用。转录组数据分析和实验验证证实,PE 患者胎盘组织中 ACVR2A 表达下调。本研究采用CRISPR/Cas9技术,利用HTR8/SVneo和JAR细胞系研究了ACVR2A基因缺失对滋养层细胞的影响。ACVR2A基因缺失会抑制滋养层细胞的迁移、增殖和侵袭,突显了它在细胞功能中的关键作用。RNA-seq数据分析揭示了一个受ACVR2A基因敲除影响的复杂调控网络,尤其是在TCF7/c-JUN通路中。通过 RT-PCR 和免疫组化分析,假设并证实了 ACVR2A 与 TCF7/c-JUN 通路之间的潜在关联。研究强调了 PE 发病的复杂性和遗传因素的重要性,尤其是在 GWAS 中发现的 ACVR2A 基因的作用。这项研究为深入研究 PE 的复杂机制奠定了坚实的基础,为有针对性的早期干预、个性化治疗和加强产科保健铺平了道路。
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ACVR2A Facilitates Trophoblast Cell Invasion through TCF7/c-JUN Pathway in Pre-eclampsia Progression
Pre-eclampsia (PE) is a serious pregnancy disorder linked to genetic factors, particularly the ACVR2A gene, which encodes a receptor involved in the activin signaling pathway and plays a critical role in reproductive processes. Transcriptomic data analysis and experimental verification confirmed a downregulation of ACVR2A expression in placental tissues from PE patients. In this study, CRISPR/Cas9 technology was employed to investigate the effect of ACVR2A gene deletion on trophoblast cells using the HTR8/SVneo and JAR cell lines.. Deletion of ACVR2A inhibits trophoblastic migration, proliferation, and invasion, underscoring its pivotal role in cellular function. RNA-seq data analysis unveiled an intricate regulatory network influenced by ACVR2A gene knockout, especially in the TCF7/c-JUN pathway. By employing RT-PCR and immunohistochemical analysis, a potential association between ACVR2A and the TCF7/c-JUN pathway was hypothesized and confirmed. The complexity of PE onset and the significance of genetic factors were emphasized, particularly the role of the ACVR2A gene identified in GWAS. This study established a robust foundation for delving deeper into the intricate mechanisms of PE, paving the way for focused early intervention, personalized treatment, and enhanced obstetric healthcare.
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