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首页> 外文期刊>Endocrinology >The absence of ER-β results in altered gene expression in ovarian granulosa cells isolated from in vivo preovulatory follicles
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The absence of ER-β results in altered gene expression in ovarian granulosa cells isolated from in vivo preovulatory follicles

机译:ER-β的缺乏导致从体内排卵前卵泡分离的卵巢颗粒细胞中基因表达的改变

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Determining the spatial and temporal expression of genes involved in the ovulatory pathway is critical for the understanding of the role of each estrogen receptor in the modulation of folliculogenesis and ovulation. Estrogen receptor (ER)-β is highly expressed in ovarian granulosa cells, and mice lacking ER-β are subfertile due to inefficient ovulation. Previous work has focused on isolated granulosa cells or cultured follicles and, although informative, provides confounding results due to the heterogeneous cell types present including granulosa and theca cells and oocytes and exposure to in vitro conditions. Herein we isolated preovulatory granulosa cells from wild-type (WT) and ERβ-null mice using laser capture microdissection to examine the genomic transcriptional response downstream of pregnant mare serum gonadotropin (mimicking FSH) and pregnant mare serum gonadotropin/human chorionic gonadotropin (mimicking LH) stimulation. This allows for a direct comparison of in vivo granulosa cells at the same stage of development from both WT and ERβ-null ovaries. ERβ-null granulosa cells showed altered expression of genes known to be regulated by FSH ( Akap12 and Runx2 ) as well as not previously reported (Arnt2 and Pou5f1 ) inWT granulosa cells. Our analysis also identified 304 genes not previously associated with ERβ in granulosa cells. LH-responsive genes including Abcb1b and Fam110c show reduced expression in ERβ-null granulosa cells; however, novel genes including Rassf2 and Megf10 were also identified as being downstream of LH signaling in granulosa cells. Collectively, our data suggest that granulosa cells from ERβ-null ovaries may not be appropriately differentiated and are unable to respond properly to gonadotropin stimulation.
机译:确定参与排卵途径的基因的时空表达对于理解每种雌激素受体在卵泡生成和排卵调节中的作用至关重要。雌激素受体(ER)-β在卵巢颗粒细胞中高表达,而缺乏ER-β的小鼠由于排卵效率低而不能生育。先前的工作集中在分离的颗粒细胞或培养的卵泡上,尽管提供了信息,但由于存在异质细胞类型(包括颗粒细胞,卵泡膜细胞和卵母细胞)以及暴露于体外条件,因此提供了令人困惑的结果。本文中,我们使用激光捕获显微切割技术从野生型(WT)和ERβ-null小鼠中分离了排卵前的颗粒细胞,以检查母马血清促性腺激素(模仿FSH)和母马血清促性腺激素/人绒毛膜促性腺激素(模仿LH)下游的基因组转录反应)刺激。这允许直接比较WT和ERβ缺失卵巢处于同一发育阶段的体内颗粒细胞。 ERβ-空颗粒细胞在WT颗粒细胞中表现出已知受FSH(Akap12和Runx2)调节的基因表达的改变,以及以前没有报道(Arnt2和Pou5f1)。我们的分析还确定了304个先前与颗粒细胞中的ERβ不相关的基因。包括Abcb1b和Fam110c在内的LH反应基因在ERβ-空颗粒细胞中表达降低;然而,还发现包括Rassf2和Megf10在内的新基因位于颗粒细胞中LH信号的下游。总体而言,我们的数据表明,来自ERβ无效卵巢的颗粒细胞可能未得到适当分化,并且无法对促性腺激素刺激做出适当反应。

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