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Endometrial Exosomes/Microvesicles in the Uterine Microenvironment: A New Paradigm for Embryo-Endometrial Cross Talk at Implantation

机译:子宫内膜外来体/子宫微环境的微泡:一种新的范式胚胎 - 子宫内膜相声在植入

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摘要

Exosomes are nanoparticles (∼100 nm diameter) released from cells, which can transfer small RNAs and mRNA via the extracellular environment to cells at distant sites. We hypothesised that exosomes or the slightly larger microvesicles (100–300 nm) are released from the endometrial epithelium into the uterine cavity, and that these contain specific micro (mi)RNA that could be transferred to either the trophectodermal cells of the blastocyst or to endometrial epithelial cells, to promote implantation. The aim of this study was to specifically identify and characterise exosomes/microvesicles (mv) released from endometrial epithelial cells and to determine whether exosomes/mv are present in uterine fluid. Immunostaining demonstrated that the tetraspanins, CD9 and CD63 used as cell surface markers of exosomes are present on the apical surfaces of endometrial epithelial cells in tissue sections taken across the menstrual cycle: CD63 showed cyclical regulation. Exosome/mv pellets were prepared from culture medium of endometrial epithelial cell (ECC1 cells) and from uterine fluid and its associated mucus by sequential ultracentifugation. Exosomes/mv were positively identified in all preparations by FACS and immunofluorescence staining following exosome binding to beads. Size particle analysis confirmed the predominance of particles of 50–150 nm in each of these fluids. MiRNA analysis of the ECC1 cells and their exosomes/mv demonstrated sorting of miRNA into exosomes/mv: 13 of the 227 miRNA were specific to exosomes/mv, while a further 5 were not present in these. The most abundant miRNA in exosomes/mv were hsa-miR-200c, hsa-miR-17 and hsa-miR-106a. Bioinformatic analysis showed that the exosome/mv-specific miRNAs have potential targets in biological pathways highly relevant for embryo implantation. Thus exosomes/mv containing specific miRNA are present in the microenvironment in which embryo implantation occurs and may contribute to the endometrial-embryo cross talk essential for this process.
机译:外泌体是从细胞释放的纳米颗粒(直径约100 nm),可以通过细胞外环境将小的RN​​A和mRNA转移到远处的细胞。我们假设外泌体或稍大的微囊泡(100-300 nm)从子宫内膜上皮释放到子宫腔,并且它们含有特定的微小(mi)RNA,可以转移到胚泡的滋养皮细胞或子宫内膜中。子宫内膜上皮细胞,促进着床。这项研究的目的是特异性鉴定和表征从子宫内膜上皮细胞释放的外泌体/微囊泡(mv),并确定子宫液中是否存在外泌体/ mv。免疫染色表明,用作外泌体细胞表面标志物的四跨膜蛋白,CD9和CD63存在于整个月经周期的组织切片中的子宫内膜上皮细胞的顶表面上:CD63显示出周期性调节作用。通过顺序超速离心从子宫内膜上皮细胞(ECC1细胞)的培养基,子宫液及其相关粘液制备外泌体/ mv沉淀。外泌体与珠子结合后,通过FACS和免疫荧光染色在所有制剂中均阳性鉴定了外泌体/ mv。粒度分析证实了每种流体中50-150 nm的颗粒占主导地位。 ECC1细胞及其外泌体/ mv的miRNA分析表明,将miRNA排序为外泌体/ mv:227个miRNA中有13种是特异于外泌体/ mv的,而另外5种则不存在。外来体/ mv中最丰富的miRNA是hsa-miR-200c,hsa-miR-17和hsa-miR-106a。生物信息学分析表明,外泌体/ mv特异性miRNA在与胚胎植入高度相关的生物学途径中具有潜在的靶标。因此,在包含胚胎植入的微环境中存在含有特定miRNA的外泌体/ mv,并且可能促成该过程必不可少的子宫内膜与胚胎的串扰。

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