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β-连环蛋白和 Dickkopf-1 在正常和子痫前期妊娠第 3 孕期胎盘的差异表达:一项对比研究。

Differential expression of β-catenin and Dickkopf-1 in the third trimester placentas from normal and preeclamptic pregnancies: a comparative study.

机构信息

Department of Clinical Laboratory, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Reprod Biol Endocrinol. 2013 Mar 4;11:17. doi: 10.1186/1477-7827-11-17.

Abstract

BACKGROUND

Beta-catenin is a key nuclear effector of Wnt signaling which could be antagonized by dickkopf-1(DKK1). Beta-catenin and DKK1 are involved in a variety of biological processes; however, their expression in the placenta with severe preeclampsia (PE) has not been elucidated. This study was aimed to detect the localization and compare the expression of beta-catenin and DKK1 in normal and preeclamptic placenta.

METHODS

Sixty pregnant women who underwent cesarean section were enrolled in this study, including 30 healthy pregnant women in the control group and 30 preeclamptic women in the severe PE group. Real-time polymerase chain reaction (real-time-PCR) and western blot were employed to detect the beta-catenin and DKK1 mRNA and protein expression levels, respectively, and their locations were evaluated by immunohistochemistry (IHC).

RESULTS

Our results indicated that beta-catenin and DKK1 were expressed predominantly in the syncytiotrophoblast and the extravillous trophoblast (EVT). The beta-catenin mRNA and protein expressions were significantly decreased, whereas the DKK1 significantly increased in preeclamptic placental tissues compared to normal placental controls.

CONCLUSIONS

In conclusion, decreased beta-catenin expression, as well as DKK1 over-expression might be associated with the process of the pathogenesis of PE. Further studies would elucidate their exact roles in the pathogenesis of PE.

摘要

背景

β-连环蛋白是 Wnt 信号的关键核效应物,可被 Dickkopf-1(DKK1)拮抗。β-连环蛋白和 DKK1 参与多种生物学过程;然而,它们在严重先兆子痫(PE)胎盘中的表达尚未阐明。本研究旨在检测β-连环蛋白和 DKK1 在正常和先兆子痫胎盘中的定位并比较其表达。

方法

本研究纳入了 60 名接受剖宫产术的孕妇,包括 30 名健康孕妇(对照组)和 30 名严重 PE 孕妇(PE 组)。采用实时聚合酶链反应(real-time-PCR)和 Western blot 分别检测β-连环蛋白和 DKK1 mRNA 和蛋白表达水平,并通过免疫组织化学(IHC)评估其定位。

结果

结果表明,β-连环蛋白和 DKK1 主要表达于合体滋养层和细胞滋养层外胚层(EVT)。与正常胎盘对照相比,PE 胎盘组织中β-连环蛋白 mRNA 和蛋白表达显著降低,而 DKK1 表达显著增加。

结论

总之,β-连环蛋白表达降低以及 DKK1 过度表达可能与 PE 发病机制过程有关。进一步的研究将阐明它们在 PE 发病机制中的确切作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afec/3599361/0823fa20ddc3/1477-7827-11-17-1.jpg

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