首页> 美国卫生研究院文献>Journal of Pregnancy >Differential Gene Expression Analysis of Placentas with Increased Vascular Resistance and Pre-Eclampsia Using Whole-Genome Microarrays
【2h】

Differential Gene Expression Analysis of Placentas with Increased Vascular Resistance and Pre-Eclampsia Using Whole-Genome Microarrays

机译:使用全基因组芯片的血管阻力增加和先兆子痫的胎盘差异基因表达分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pre-eclampsia is a pregnancy complication characterized by hypertension and proteinuria. There are several factors associated with an increased risk of developing pre-eclampsia, one of which is increased uterine artery resistance, referred to as “notching”. However, some women do not progress into pre-eclampsia whereas others may have a higher risk of doing so. The placenta, central in pre-eclampsia pathology, may express genes associated with either protection or progression into pre-eclampsia. In order to search for genes associated with protection or progression, whole-genome profiling was performed. Placental tissue from 15 controls, 10 pre-eclamptic, 5 pre-eclampsia with notching, and 5 with notching only were analyzed using microarray and antibody microarrays to study some of the same gene product and functionally related ones. The microarray showed 148 genes to be significantly altered between the four groups. In the preeclamptic group compared to notch only, there was increased expression of genes related to chemotaxis and the NF-kappa B pathway and decreased expression of genes related to antigen processing and presentation, such as human leukocyte antigen B. Our results indicate that progression of pre-eclampsia from notching may involve the development of inflammation. Increased expression of antigen-presenting genes, as seen in the notch-only placenta, may prevent this inflammatory response and, thereby, protect the patient from developing pre-eclampsia.
机译:子痫前期是一种以高血压和蛋白尿为特征的妊娠并发症。有多种因素与子痫前期风险增加有关,其中之一是子宫动脉阻力增加,称为“切口”。但是,有些妇女没有发展为先兆子痫,而另一些妇女则有更高的风险。子痫前期病理的中心胎盘可能表达与保护或进展为子痫前期有关的基因。为了搜索与保护或进展相关的基因,进行了全基因组分析。使用微阵列和抗体微阵列分析了来自15个对照,10个先兆子痫,5个先兆子痫,5个先切口的胎盘组织,以研究一些相同的基因产物和功能相关的产物。微阵列显示四组之间有148个基因发生了显着改变。在先兆子痫组中,与仅缺口相比,与趋化性和NF-κB通路相关的基因表达增加,而与抗原加工和呈递相关的基因(例如人白细胞抗原B)的表达下降。我们的结果表明,子痫前期的切口可能涉及炎症的发展。如仅在缺刻的胎盘中所见,抗原呈递基因的表达增加可以预防这种炎症反应,从而保护患者免于先兆子痫的发作。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号