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首页> 外文期刊>Journal of Reproductive Immunology >Distinct microRNA expression in endometrial lymphocytes, endometrium, and trophoblast during spontaneous porcine fetal loss
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Distinct microRNA expression in endometrial lymphocytes, endometrium, and trophoblast during spontaneous porcine fetal loss

机译:自发性猪胎儿丢失过程中子宫内膜淋巴细胞,子宫内膜和滋养细胞中不同的microRNA表达

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Endometrial lymphocytes are recruited to the porcine maternal-fetal interface by conceptus-derived signals. The transiently recruited lymphocytes adopt a specialized phenotype in the endometrium that regulates various placental physiological processes, including angiogenesis. Small non-coding RNAs, microRNAs (miRNAs) are emerging as principal bio-molecules regulating the development of lymphocytes and their angiogenic functions. However, no information is available in the context of endometrial lymphocytes in pregnancy. We hypothesize that miRNAs are involved in the development of endometrial lymphocytes and their angiogenic functions at the porcine maternal-fetal interface. Using a targeted Q-PCR approach for selected miRNAs involved in immune cell development, angiogenesis, and anti-angiogenesis, we conducted a study to screen endometrial lymphocytes associated with healthy and spontaneously arresting conceptus attachment sites (CAS) at two well-defined periods of fetal loss. Comparisons were made with endometrium and trophoblasts associated with healthy and arresting CAS. In addition, levels of putative mRNA targets and subsequent functional clustering of genes were studied in order to predict the biological mechanisms affected. We found several significant differences for miRNAs involved in immune cell development and angiogenesis (miR-296-5P, miR-150, miR-17P-5P, miR-18a, and miR-19a) between endometrial lymphocytes associated with healthy and arresting CAS. Significant differences were also found in endometrium and trophoblasts for some miRNAs (miR-20b, miR-17-5P, miR-18a, miR-15b-5P, and miR-222). Finally, selected mRNA targets showed differential expression in all groups. Our data, although associative, are the first to unravel the selected miRNAs involved in immune cell development and provide insights into their possible regulation in abortive pregnancy. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:子宫内膜淋巴细胞通过概念来源的信号募集到猪母胎界面。短暂募集的淋巴细胞在子宫内膜采取特殊的表型,调节各种胎盘生理过程,包括血管生成。小型非编码RNA,微小RNA(miRNA)逐渐成为调节淋巴细胞发育及其血管生成功能的主要生物分子。但是,在妊娠中子宫内膜淋巴细胞方面没有可用的信息。我们假设,miRNA参与了子宫内膜淋巴细胞的发展及其在猪母胎界面的血管生成功能。使用针对性的Q-PCR方法对参与免疫细胞发育,血管生成和抗血管生成的选定miRNA进行研究,我们进行了一项研究,以筛选在两个明确定义的时期与健康并自发停止的概念附着位点(CAS)相关的子宫内膜淋巴细胞。胎儿流失。将子宫内膜和滋养细胞与健康的和停搏的CAS进行了比较。此外,研究了推定的mRNA靶标的水平和随后的基因功能簇,以预测受影响的生物学机制。我们发现与健康和停搏CAS相关的子宫内膜淋巴细胞之间涉及免疫细胞发育和血管生成的miRNA的几个显着差异(miR-296-5P,miR-150,miR-17P-5P,miR-18a和miR-19a)。在某些miRNA(miR-20b,miR-17-5P,miR-18a,miR-15b-5P和miR-222)的子宫内膜和滋养细胞中也发现了显着差异。最后,选择的mRNA靶标在所有组中显示差异表达。我们的数据尽管具有关联性,但却是第一个揭开参与免疫细胞发育的选定miRNA的资料,并提供了对其在流产妊娠中可能的调控的见解。 (C)2014 Elsevier Ireland Ltd.保留所有权利。

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