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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Dynamic Proteomic Profiles of In Vivo- and In Vitro-Produced Mouse Postimplantation Extraembryonic Tissues and Placentas
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Dynamic Proteomic Profiles of In Vivo- and In Vitro-Produced Mouse Postimplantation Extraembryonic Tissues and Placentas

机译:体外和体外小鼠后后模木制组织和胎盘的动态蛋白质组学谱

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摘要

As the interface between the mother and the developing fetus, the placenta is believed to play an important role in assisted reproductive technology (ART)-induced aberrant intrauterine and postnatal development. However, the mechanisms underlying aberrant placentation remain unclear, especially during extraembryonic tissue development and early stages of placental formation. Using a mouse model, this investigation provides the first comparative proteomic analysis of in vivo (IVO) and in vitro-produced (IVP) extraembryonic tissues and placentas after IVO fertilization and development, or in vitro fertilization and culture, respectively. We identified 165 and 178 differentially expressed proteins (DEPs) between IVO and IVP extraembryonic tissues and placentas on Embryonic Day 7.5 (E7.5) and E10.5, respectively. Many DEPs were functionally associated with genetic information processing, such as impaired de novo DNA methylation, as well as posttranscriptional, translational and posttranslational dysregulation. These novel findings were further confirmed by global hypomethylation, and a lower level of correlation was found between the transcriptome and proteome in the IVP groups. In addition, numerous DEPs were involved in energy and amino acid metabolism, cytoskeleton organization and transport, and vasculogenesis and angiogene-sis. These disturbed processes and pathways are likely to be associated with embryonic intrauterine growth restriction, an enlarged placenta, and impaired labyrinth morphogenesis. This study provides a direct and comprehensive reference for the further exploration of the placental mechanisms that underlie ART-induced developmental aberrations.
机译:作为母亲和发展胎儿之间的界面,胎盘被认为在辅助生殖技术(艺术)诱导异常宫内和产后发育中发挥重要作用。然而,异常讲台的机制仍然不清楚,特别是在胎盘形成的超结晶组织发育和早期阶段。使用鼠标模型,本研究分别为体内(IVO)和体外产生(IVP)Impereabrynic组织和胎盘分别提供了IVO施肥和发展或体外施肥和培养后的第一种比较蛋白质组学分析。在胚胎第7.5(E7.5)和E10.5分别在IVO和IVP Imprybrysonic组织和胎盘之间鉴定了165和178型差异表达的蛋白质(DEPS)和胎儿。许多DEP在功能上与遗传信息处理有关,例如损害Novo DNA甲基化,以及术后翻译,平移和后期性失调。通过全局低甲基化进一步证实这些新发现,在IVP组中的转录组和蛋白质组之间发现了较低的相关性。此外,许多DEPS参与能量和氨基酸代谢,细胞骨架组织和运输,以及血管生成和血管生成型。这些受扰动的方法和途径可能与胚胎宫内生长限制,扩大的胎盘和迷宫式形态发生障碍有关。本研究提供了直接和全面的参考,进一步探索艺术诱导的发育畸变的胎盘机制。

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