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The effect of lysophosphatidic acid-supplemented culture medium on human immature oocytes matured in vitro

机译:溶血磷脂酸补充培养基对体外成熟的人未成熟卵母细胞的影响

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Lysophosphatidic acid-supplemented culture medium significantly increases the oocyte maturation rate in vitro. However, potential targets and pathways involved remain unknown. A total of 43 women, who underwent cesarean section and aged between 18 and 35 years with good health, were included in this study. Immature oocytes were obtained and cultured with 10 μM lysophosphatidic acid. After culture, oocyte maturation was assessed and oocytes and cumulus cells were collected for RNA sequencing. Hierarchical indexing for spliced alignment of transcripts 2 method was used to align clean reads to the human genome. The featureCounts and edgeR package were used to calculate gene expression and analyze differences between groups respectively. ClusterProfiler program was used to perform Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis. Oocyte maturation rate increased significantly following 48?h culture with lysophosphatidic acid. In cumulus cells, Gene Ontology analysis revealed the top 20 items enriched by upregulated genes and downregulated genes respectively; Kyoto Encyclopedia of Genes and Genomes analysis showed that upregulated genes in the treatment group were enriched in TNF signaling and insulin secretion pathways and downregulated genes were enriched in TNF signaling and cell adhesion molecules. In oocytes, Gene Ontology analysis revealed the top 20 items enriched by upregulated genes and downregulated genes respectively; Kyoto Encyclopedia of Genes and Genomes analysis showed that upregulated genes in the treatment group were enriched in MAPK signaling, gap junction, and cell cycle pathways and downregulated genes were enriched in MAPK signaling, estrogen signaling, RAP1 signaling, and gap junction pathways. Lysophosphatidic acid in culture medium enhances human oocyte maturation in vitro and the identified some potential pathways may associate with oocyte maturation.
机译:溶血磷脂酸补充培养基显着增加了体外卵母细胞成熟速率。然而,涉及的潜在目标和途径仍然是未知的。在本研究中,共有43名接受剖宫产和18至35岁的妇女,并在这项研究中纳入了健康。得到不成熟的卵母细胞并用10μM溶血磷脂酸培养。在培养后,评估卵母细胞成熟,并收集卵母细胞和巨积细胞用于RNA测序。用于转录物的拼接对准的分层索引2方法对人类基因组对准清洁读数。 FeatureCounts和Edger包用于计算基因表达并分析分别之间的差异。 ClusterProfiler程序用于对基因和基因组进行基因本体和京都百科全书进行分析。卵母细胞成熟率与溶血磷脂酸48μm培养显着增加。在积积菌细胞中,基因本体学分析揭示了分别由上调基因和下调基因富集的前20项;基因和基因组的京都百科全书显示,治疗组中的上调基因在TNF信号传导中富集,富含胰岛素分泌途径和下调基因在TNF信号传导和细胞粘附分子中富集。在卵母细胞中,基因本体分析揭示了富含上调基因和下调基因的前20项。基因和基因组的京都百科全书显示,治疗组中的上调基因富集在MAPK信号传导,间隙结和细胞周期途径和下调基因中,富集在MAPK信号传导,雌激素信号,RAP1信号传导和间隙结途径中。培养基中的溶血磷脂酸在体外增强人卵母细胞成熟,并且鉴定的一些潜在途径可以与卵母细胞成熟相关。

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