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叶酸缺乏对 Esr1、Cdh1 和 Pgr 启动子甲基化和基因表达的影响及其对子宫内膜容受性和胚胎着床的影响。

Effect of folate deficiency on promoter methylation and gene expression of Esr1, Cdh1 and Pgr, and its influence on endometrial receptivity and embryo implantation.

机构信息

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Box 197, No. 1 Yixueyuan Road, Yuzhong District, 400016 Chongqing, PR China.

出版信息

Hum Reprod. 2012 Sep;27(9):2756-65. doi: 10.1093/humrep/des187. Epub 2012 Jun 15.

Abstract

BACKGROUND

Folate, one of the B vitamins, provides the one-carbon units required for methylation. Folate deficiency has been associated with many pathologies. However, much less is known about the effect of it on human reproduction, especially on implantation. The establishment of uterine receptivity is crucial for successful embryo implantation. Gene expression can be influenced by both heredity and epigenetics such as DNA methylation. However, it is not known whether the methylation and expression of genes related to uterine receptivity can be affected by folate levels. To explore whether folate deficiency affected the epigenetic regulation of genes related to uterine receptivity, and their influence on implantation, we investigated the methylation and expression of cadherin 1 (Cdh1), progesterone receptor (Pgr) and estrogen receptor 1 (Esr1) genes during implantation and the implantation efficiency using a folate-deficient pregnant mouse model.

METHODS

Serum folate levels of pregnant mice were measured using the electro-chemiluminescence immunoassay. The methylation status of Cdh1, Pgr and Esr1 promoter regions was determined by methylation-specific PCR and bisulfite sequencing. The expression of Cdh1, Pgr and Esr1 in the implantation-site endometrium was examined by real-time PCR, western blot and immunohistochemistry. The number and the morphology of pinopodes, important morphological markers of endometrial receptivity, were examined using scanning electron microscopy. The number of implantation sites demarcated by distinct blue bands was recorded.

RESULTS

Serum folate levels of the folate-deficient group were lower (5.42 ± 1.35 ng/ml, n= 42) than those of the normal group (24.13 ± 4 .26 ng/ml, n= 37; P = 0.003). Here we show that the methylation status and mRNA levels of Esr1 were decreased (P= 0.021, P= 0.045, respectively), while the Cdh1 and Pgr expression levels were slightly but not significantly elevated and the methylation status did not vary in the folate-deficient mice compared with the wild type. Neither the number nor morphology of pinopodes was affected by folate deficiency. Furthermore, folate deficiency did not affect the number of implantation sites in mice.

CONCLUSIONS

This study demonstrates for the first time that, unlike the effects on Esr1, folate deficiency in mice does not influence the methylation and expression of Pgr and Cdh1, two genes shown to be essential for uterine receptivity and embryo implantation. Embryo implantation in mice appears to be unaffected by a deficiency in folate, suggesting that abnormalities in a pregnancy caused by folate deficiency start to develop after implantation.

摘要

背景

叶酸是 B 族维生素之一,提供甲基化所需的一碳单位。叶酸缺乏与许多病理有关。然而,人们对它对人类生殖的影响,尤其是对植入的影响知之甚少。建立子宫容受性对于成功的胚胎植入至关重要。基因表达可以受到遗传和表观遗传(如 DNA 甲基化)的影响。然而,目前尚不清楚与子宫容受性相关的基因的甲基化和表达是否会受到叶酸水平的影响。为了探讨叶酸缺乏是否会影响与子宫容受性相关的基因的表观遗传调控及其对植入的影响,我们使用叶酸缺乏的妊娠小鼠模型研究了植入过程中钙黏蛋白 1 (Cdh1)、孕激素受体 (Pgr)和雌激素受体 1 (Esr1) 基因的甲基化和表达及其对植入效率的影响。

方法

采用电化学发光免疫分析法测定妊娠小鼠血清叶酸水平。采用甲基化特异性 PCR 和亚硫酸氢盐测序法检测 Cdh1、Pgr 和 Esr1 启动子区的甲基化状态。采用实时 PCR、western blot 和免疫组织化学法检测植入部位子宫内膜中 Cdh1、Pgr 和 Esr1 的表达。用扫描电子显微镜观察重要的子宫内膜容受性形态学标志物- 种植窗期的突状突起的数量和形态。记录用明显蓝色带标记的植入部位数量。

结果

叶酸缺乏组血清叶酸水平较低(5.42±1.35ng/ml,n=42),明显低于正常组(24.13±4.26ng/ml,n=37;P=0.003)。我们发现 Esr1 的甲基化状态和 mRNA 水平降低(P=0.021,P=0.045),而 Cdh1 和 Pgr 的表达水平略有升高但无统计学意义,且叶酸缺乏组与野生型相比,其甲基化状态无变化。种植窗期突状突起的数量和形态均不受叶酸缺乏的影响。此外,叶酸缺乏并不影响小鼠的植入部位数量。

结论

本研究首次表明,与 Esr1 不同,叶酸缺乏对 Pgr 和 Cdh1 的甲基化和表达没有影响,这两个基因对子宫容受性和胚胎植入至关重要。小鼠的胚胎植入似乎不受叶酸缺乏的影响,这表明由叶酸缺乏引起的妊娠异常是在植入后开始发展的。

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