当前位置:首页 / CITED2通过调控滋养细胞功能参与子痫前期发病的机制研究
论著·基础研究 | 更新时间:2026-08-10
|
CITED2通过调控滋养细胞功能参与子痫前期发病的机制研究
Mechanism of CITED2 participating in the pathogenesis of preeclampsia by regulating trophoblast function: a research study

广西医学 页码:1026-1032

作者机构:陆秀景,硕士,住院医师,研究方向为围产医学与高危妊娠。

基金信息:广西自然科学基金(2024GXNSFAA010368);广西医疗卫生适宜技术开发与推广应用项目(S2022080);广西医科大学第一附属医院优秀医学英才培养计划(〔优秀医学英才〕202107号)

DOI:10.11675/j.issn.0253⁃4304.2026.07.13

  • 中文简介
  • 英文简介
  • 参考文献

目的 探讨Cbp/p300相互作用反式激活因子2(CITED2)过表达对人绒毛膜滋养层细胞HTR⁃8/Svneo增殖、迁移、侵袭及凋亡功能的调控作用,为阐明子痫前期(PE)发病机制提供新思路。方法 将HTR⁃8/Svneo细胞分为过表达组(转染CITED2过表达质粒)和空载组(转染空载质粒)。通过实时荧光定量PCR和Western blot验证转染效率后,分别采用CCK⁃8法、划痕实验、Transwell实验和流式细胞术系统评估CITED2过表达对滋养细胞增殖、迁移、侵袭及凋亡的影响。结果 CCK⁃8实验结果显示,在培养48 h、72 h、96 h后,过表达组的吸光度值高于空载组(P<0.05)。划痕实验结果表明,划痕24 h后,过表达组的细胞迁移率高于空载组(P<0.05)。Transwell实验结果显示,过表达组的穿膜细胞数多于空载组(P<0.001)。流式细胞术检测结果显示,与空载组相比,过表达组的细胞凋亡率降低(P<0.05)。结论 CITED2可通过促进滋养细胞增殖、迁移和侵袭并抑制其凋亡,在PE发生和发展过程中发挥保护作用。

Objective To investigate the regulatory effects of Cbp/p300‑interacting transactivator with Glu/Asp rich carboxy⁃terminal domain 2 (CITED2) overexpression on the proliferation, migration, invasion, and apoptosis of extravillous trophoblast HTR‑8/Svneo cells, providing new insights into the pathogenesis of preeclampsia (PE). Methods HTR‑8/Svneo cells were assigned to overexpression group (with the transfection of CITED2 overexpression plasmid) or empty vector group (with the transfection of empty vector plasmid). After the validation of the transfection efficiency by using real⁃time fluorescent quantitative PCR and Western blot, the effects of CITED2 overexpression on trophoblast proliferation, migration, invasion, and apoptosis were systematically evaluated via CCK‑8 assay, wound‑healing assay, Transwell assay, and flow cytometry, respectively. Results The CCK‑8 assay results revealed that at 48, 72, and 96 hours post‑culture, the absorbance value in the overexpression group was higher than that in the empty vector group (P<0.05). The wound‑healing assay demonstrated that at 24 hours after scratching, the cell migration rate in the overexpression group was higher than that in the empty vector group (P<0.05). The Transwell assay revealed that the number of transmembrane cells in the overexpression group was more than that in the empty vector group (P<0.001). Flow cytometry results indicated that the cell apoptosis rate in the overexpression group was lower than that in the empty vector group (P<0.05). Conclusion CITED2 exerts protective effect during the occurrence and development of PE through promoting proliferation, migration, invasion of trophoblast, and inhibiting their apoptosis.

12

浏览量

1

下载量

0

CSCD

工具集