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白细胞介素-1β和转化生长因子-β通过破坏紧密连接削弱胎盘屏障:一项体内和体外研究

IL-1β and TGF-β weaken the placental barrier through destruction of tight junctions: an in vivo and in vitro study.

作者信息

Tossetta G, Paolinelli F, Avellini C, Salvolini E, Ciarmela P, Lorenzi T, Emanuelli M, Toti P, Giuliante R, Gesuita R, Crescimanno C, Voltolini C, Di Primio R, Petraglia F, Castellucci M, Marzioni D

机构信息

Department of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60020 Ancona, Italy.

Department of Molecular and Clinical Sciences-Histology, Università Politecnica delle Marche, 60020 Ancona, Italy.

出版信息

Placenta. 2014 Jul;35(7):509-16. doi: 10.1016/j.placenta.2014.03.016. Epub 2014 Apr 15.

Abstract

INTRODUCTION

Chorioamnionitis is a gestational pathological condition characterized by acute inflammation of the amniochorionic membranes and placentas leading to high concentrations of IL-1β, Il-6, Il-8 and TGF-β in the amniotic fluid. In normal conditions, the permeability of foeto-maternal barrier is due to the assembly and maintenance of different cellular junctional domains.

METHODS

In the present study, first we aimed to evaluate the protein expression (by immunohistochemistry and western blotting) and mRNA (by real time PCR) levels of the molecular components of tight junctions (Zonula occludens-1 and occludin), and of adherent junctions (VE-cadherin and β-catenin) in placentas from chorioamnionitis compared to that in normal pregnancies.

RESULTS

Western blotting results showed a significant down-regulation of occludin in placentas affected with chorioamnionitis. No differences were detected for the other proteins analysed. We evaluated whether occludin expression was regulated by IL-1β, IL-6, IL-8 and TGF-β by means of in vitro studies using HUVEC cultures and demonstrated a key role of IL-1β and TGF-β in the disappearance of occludin at cellular border.

CONCLUSIONS

We conclude by suggesting a pivotal role of these two cytokines in facilitating intra-placental infection via para-cellular way due to the disassembly of tight junctions at trophoblastic and endothelial cells in placental tissues.

摘要

引言

绒毛膜羊膜炎是一种妊娠病理状态,其特征为羊膜绒毛膜和胎盘的急性炎症,导致羊水内白细胞介素-1β、白细胞介素-6、白细胞介素-8和转化生长因子-β浓度升高。在正常情况下,母胎屏障的通透性归因于不同细胞连接结构域的组装和维持。

方法

在本研究中,首先我们旨在通过免疫组织化学和蛋白质印迹法评估绒毛膜羊膜炎患者胎盘与正常妊娠胎盘相比紧密连接分子成分(闭合蛋白和闭合小环蛋白-1)以及黏附连接分子成分(血管内皮钙黏蛋白和β-连环蛋白)的蛋白表达水平,并通过实时聚合酶链反应评估其信使核糖核酸水平。

结果

蛋白质印迹结果显示,绒毛膜羊膜炎患者胎盘的闭合蛋白显著下调。对分析的其他蛋白质未检测到差异。我们通过使用人脐静脉内皮细胞培养物进行体外研究,评估闭合蛋白表达是否受白细胞介素-1β、白细胞介素-6、白细胞介素-8和转化生长因子-β的调节,并证明白细胞介素-1β和转化生长因子-β在细胞边界闭合蛋白消失中起关键作用。

结论

我们通过研究得出结论,这两种细胞因子在促进胎盘内感染方面起着关键作用,其通过胎盘组织中滋养层细胞和内皮细胞紧密连接的解体,经细胞旁途径实现感染。

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