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首页> 外文期刊>Reviews of Reproduction >Placental development during early pregnancy in sheep: cell proliferation, global methylation, and angiogenesis in the fetal placenta
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Placental development during early pregnancy in sheep: cell proliferation, global methylation, and angiogenesis in the fetal placenta

机译:绵羊妊娠早期胎盘发育:胎儿胎盘中的细胞增殖,整体甲基化和血管生成

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摘要

To characterize early fetal placental development, gravid uterine tissues were collected from pregnant ewes every other day from day 16 to 30 after mating. Determination of 1) cell proliferation was based on Ki67 protein immunodetection; 2) global methylation was based on 5-methyl-cytosine (5mC) expression and mRNA expression for DNA methyltransferases (DNMTs) 1, 3a, and 3b; and 3) vascular development was based on smooth muscle cell actin immunolocalization and on mRNA expression of several factors involved in the regulation of angiogenesis in fetal membranes (FMs). Throughout early pregnancy, the labeling index (proportion of proliferating cells) was very high (21%) and did not change. Expression of 5mC and mRNA for DNMT3b decreased, but mRNA for DNMT1 and 3a increased. Blood vessels were detected in FM on days 18–30 of pregnancy, and their number per tissue area did not change. The patterns of mRNA expression for placental growth factor, vascular endothelial growth factor, and their receptors FLT1 and KDR; angiopoietins 1 and 2 and their receptor TEK; endothelial nitric oxide synthase and the NO receptor GUCY13B; and hypoxia inducing factor 1 α changed in FM during early pregnancy. These data demonstrate high cellular proliferation rates, and changes in global methylation and mRNA expression of factors involved in the regulation of DNA methylation and angiogenesis in FM during early pregnancy. This description of cellular and molecular changes in FM during early pregnancy will provide the foundation for determining the basis of altered placental development in pregnancies compromised by environmental, genetic, or other factors.
机译:为了表征胎儿胎盘的早期发育,从交配后第16天到第30天每隔一天从怀孕的母羊中收集妊娠子宫组织。 1)细胞增殖的测定基于Ki67蛋白免疫检测; 2)全局甲基化基于DNA甲基转移酶(DNMT)1、3a和3b的5-甲基胞嘧啶(5mC)表达和mRNA表达; 3)血管的发育基于平滑肌细胞肌动蛋白的免疫定位以及胎膜(FMs)血管生成调控中涉及的几种因子的mRNA表达。在整个怀孕初期,标记指数(增殖细胞的比例)非常高(21%),并且没有变化。 DNMT3b的5mC和mRNA的表达减少,但DNMT1和3a的mRNA的表达增加。在怀孕的第18-30天在FM中检测到血管,并且每个组织区域的血管数量没有变化。胎盘生长因子,血管内皮生长因子及其受体FLT1和KDR的mRNA表达模式;血管生成素1和2及其受体TEK;内皮型一氧化氮合酶和NO受体GUCY13B;妊娠早期FM中的低氧诱导因子1α发生了变化。这些数据表明,在妊娠早期,FM的DNA甲基化和血管生成调控中涉及的因子的高细胞增殖率以及总体甲基化和mRNA表达的变化。妊娠早期FM中细胞和分子变化的描述将为确定受环境,遗传或其他因素影响的妊娠中胎盘发育改变的基础提供基础。

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