...
首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Gene and protein expression signature of endometrial glandular and stromal compartments during the window of implantation
【24h】

Gene and protein expression signature of endometrial glandular and stromal compartments during the window of implantation

机译:着床期间子宫内膜腺体和间质区室的基因和蛋白质表达特征

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: To map the changes in messenger RNA (mRNA) and protein abundance during the window of implantation in specifically endometrial stromal and glandular epithelial cells obtained using laser microdissection microscopy (LDM). Design: Endometrial samples were collected from two menstrual cycles at 2 and 7 days after first significant rise in blood LH, and separate cell populations were obtained using LDM. A new generation linear polymerase chain reaction (PCR) amplified the mRNA, which were hybridized to both Affymetrix U133 Plus2 and Agilent 4x44K microarrays followed by gene set analysis. Immunohistochemistry assessed protein expression between the two collection times. Setting: In vitro fertilization clinic. Patient(s): Nine Caucasian, fertile, cycling women. Intervention(s): None. Main Outcome Measure(s): Cycle dating using blood markers; microarrays on laser microdissected glands and stroma; dual platform microarray confirmation; immunohistochemical analysis of cell cycle proteins. Result(s): The two microarray platforms showed concordance. During the window of implantation, a statistically significant network of 22 mRNA associated with the cell cycle was down-regulated. Immunohistochemistry identified altered localization in stroma. Conclusion(s): Microarrays demonstrated glands and stroma have distinct mRNA signatures, each dependent on the day of the cycle. We characterized two compartments of the receptive endometrium with a transcriptomic signature identifying regulation of only the cell cycle. Immunohistochemical analysis of cell cycle proteins identified a signature staining pattern of nuclear relocalization of a group of cyclins of stromal cells, which may be clinically applicable.
机译:目的:绘制通过激光显微切割显微镜(LDM)获得的子宫内膜基质和腺上皮细胞在植入窗口期间信使RNA(mRNA)和蛋白质丰度的变化图。设计:在血液中LH首次显着升高后的第2天和第7天,从两个月经周期收集子宫内膜样品,并使用LDM获得单独的细胞群。新一代线性聚合酶链反应(PCR)扩增了mRNA,并将其与Affymetrix U133 Plus2和Agilent 4x44K微阵列杂交,然后进行基因组分析。免疫组织化学评估了两个收集时间之间的蛋白质表达。地点:体外受精诊所。患者:九名白人,可育,骑自行车的妇女。干预措施:无。主要观察指标:使用血液标记物进行循环约会;激光显微切割的腺体和基质上的微阵列;双平台微阵列确认;细胞周期蛋白的免疫组织化学分析。结果:两个微阵列平台显示出一致性。在植入窗口期间,与细胞周期相关的22个mRNA的统计显着网络被下调。免疫组织化学鉴定了基质中定位的改变。结论:微阵列显示腺体和间质具有不同的mRNA特征,每个特征均取决于周期的一天。我们用仅识别细胞周期调控的转录组特征来表征子宫内膜的两个区室。细胞周期蛋白的免疫组织化学分析确定了一组基质细胞周期蛋白核重定位的标志性染色模式,这可能在临床上适用。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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