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环境污染物苯并[a]芘通过促进绒毛外滋养层细胞凋亡和抑制迁移诱导复发性流产。

Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast.

机构信息

Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou, 510120 Guangdong, China.

Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou, 510120 Guangdong, China.

出版信息

Biomed Res Int. 2020 Oct 16;2020:8983494. doi: 10.1155/2020/8983494. eCollection 2020.

Abstract

METHODS

The implantation sites, fetus resorption, and abnormal fetuses were studied in pregnant mice treated with different doses of BaP by oral gavage from day 1 to day 10 of gestation. Additionally, apoptosis and related signaling pathway, and the migration and invasion of trophoblasts, were assessed before and after exposure of BPDE in Swan 71 trophoblast cell. Besides, the migration and invasion, and its related signaling pathway, were assessed in villi obtained from women.

RESULTS

We observed a concentration-dependent incidence of abnormal murine fetuses, beginning with 0.1 mg/kg BaP; with a BaP concentration of 2 mg/kg, no fetuses developed. Correspondingly, a BPDE concentration-dependent apoptosis of human trophoblasts. Beginning with 0.5 M BPDE exposure, Bax/Caspase-3 were increased and Bcl-2 decreased. Furthermore, BPDE also inhibited, in a dose-dependent manner, the migration of villous explants from elective abortion women, consistent with the reduced migration of villous explants from women with recurrent pregnancy loss (RPL), and reduced the cell immigration in Swan 71 trophoblasts, in a dose-dependent manner measured by transwell assays.

CONCLUSIONS

Our study results provide mechanistic insight to the effect of BPDE on trophoblast dysfunction through enhanced cell apoptosis and inhibited migration, providing further experimental evidence to the causative links between BaP exposure and PRL.

摘要

方法

通过口服灌胃,从妊娠第 1 天到第 10 天,对不同剂量 BaP 处理的怀孕小鼠进行植入部位、胎儿吸收和异常胎儿研究。此外,在 Swan 71 滋养细胞暴露于 BPDE 前后,评估了细胞凋亡及其相关信号通路,以及滋养细胞的迁移和侵袭。此外,还评估了从人工流产妇女获得的绒毛中的迁移和侵袭及其相关信号通路。

结果

我们观察到异常胎鼠的发生率呈浓度依赖性,从 0.1mg/kg BaP 开始;当 BaP 浓度为 2mg/kg 时,没有胎儿发育。相应地,人滋养细胞的 BPDE 浓度依赖性凋亡。从 0.5μM BPDE 暴露开始,Bax/Caspase-3 增加,Bcl-2 减少。此外,BPDE 还以剂量依赖性方式抑制选择性流产妇女绒毛外植体的迁移,与复发性妊娠丢失(RPL)妇女的绒毛外植体迁移减少一致,并且通过 Transwell 测定,以剂量依赖性方式减少 Swan 71 滋养细胞中的细胞迁移。

结论

我们的研究结果提供了 BPDE 通过增强细胞凋亡和抑制迁移对滋养细胞功能障碍的影响的机制见解,为 BaP 暴露与 PRL 之间的因果关系提供了进一步的实验证据。

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