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子痫前期和胎儿生长受限中的基质金属蛋白酶 1:蜕膜组织中基因表达降低,绒毛外滋养细胞中蛋白表达增加。

Matrix metalloproteinase 1 in pre-eclampsia and fetal growth restriction: reduced gene expression in decidual tissue and protein expression in extravillous trophoblasts.

机构信息

Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Olav Kyrres gate 11, Trondheim, Norway.

出版信息

Placenta. 2010 Jul;31(7):615-20. doi: 10.1016/j.placenta.2010.04.003. Epub 2010 May 8.

Abstract

Superficial invasion of extravillous trophoblasts (EVTs) and impaired spiral artery remodelling are characterizing phenomena in pregnancies complicated by pre-eclampsia (PE) and fetal growth restriction (FGR). However, the underlying causes remain unclear. In this study, gene expression in decidua basalis tissue from pregnancies complicated with PE and/or FGR (n = 18) and normal pregnancies (n = 17) was assessed by Affymetrix HG Focus microarray to obtain hints of mechanisms involved in the pathogenesis. A total of 200 differentially expressed transcripts were detected at a false discovery rate (FDR) <or= 0.1. Several genes involved in trophoblast differentiation and invasion were downregulated, including the matrix metalloproteinases (MMPs) MMP1, -7 and -12. MMPs are a family of enzymes involved in degradation of extracellular matrix and have been ascribed a permissive role in trophoblast invasion. MMP1 had the highest fold change among the differentially expressed genes (four-fold downregulated) and was chosen for further investigation. Reduced MMP1 mRNA in decidual tissue was confirmed by RT-qPCR. MMP1 protein expression in EVTs was assessed by double immunofluorescence analysis, using antibodies against pro-MMP1 and cytokeratin 7. The proportion of MMP1 positive EVTs was reduced in all subgroups of cases (PE: n = 18, FGR: n = 11 and PE + FGR: n = 30) compared to controls (n = 23) (all p's < 0.05). Based on these findings, we hypothesize that reduced levels of MMP1 protein in EVTs could be linked to the impaired trophoblast invasion in PE and/or FGR.

摘要

滋养细胞外突(EVTs)的浅层浸润和螺旋动脉重塑受损是子痫前期(PE)和胎儿生长受限(FGR)合并妊娠的特征性现象。然而,其根本原因仍不清楚。本研究通过 Affymetrix HG Focus 微阵列评估了合并 PE 和/或 FGR(n = 18)及正常妊娠(n = 17)的妊娠蜕膜组织中的基因表达,以获得参与发病机制的相关机制的线索。在 FDR < 0.1 时检测到 200 个差异表达的转录本。几个参与滋养细胞分化和浸润的基因下调,包括基质金属蛋白酶(MMPs)MMP1、-7 和 -12。MMPs 是一组参与细胞外基质降解的酶,在滋养细胞浸润中具有允许作用。差异表达基因中 MMP1 的倍数变化最高(下调四倍),因此选择其进行进一步研究。通过 RT-qPCR 证实蜕膜组织中 MMP1 mRNA 减少。通过双免疫荧光分析用抗 pro-MMP1 和细胞角蛋白 7 的抗体评估 EVT 中的 MMP1 蛋白表达。与对照组(n = 23)相比,所有病例亚组(PE:n = 18、FGR:n = 11 和 PE + FGR:n = 30)的 MMP1 阳性 EVT 比例均降低(均 p < 0.05)。基于这些发现,我们假设 EVT 中 MMP1 蛋白水平降低可能与 PE 和/或 FGR 中滋养细胞浸润受损有关。

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