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首页> 外文期刊>Molecular human reproduction. >Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases gap junction intercellular communication activity inimmortalized human granulosa cells
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Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases gap junction intercellular communication activity inimmortalized human granulosa cells

机译:卵母细胞衍生的BMP15而不是GDF9下调连接蛋白43的表达并降低永生化人类颗粒细胞的间隙连接细胞间通讯活性

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摘要

In the ovary, connexin-coupled gap junctions in granulosa cells play crucial roles in follicular and oocyte development as well as in corpus luteum formation. Our previous work has shown that theca cell-derived bone morphogenetic protein (BMP)4 and BMP7 decrease gap junction intercellular communication (GJIC) activity via the down-regulation of connexin43 (C×43) expression in immortalized human granulosa cells. However, the effects of oocyte-derived growth factors on C×43 expression remain to be elucidated. The present study was designed to investigate the effects of oocyte-derived growth differentiation factor (GDF)9 and BMP15 on the expression of C×43 in a human granulosa cell line, SVOG. We also examined the effect relative to GJIC activity and investigated the potential mechanisms of action. In SVOG cells, treatment with BMP15 but not GDF9 significantly decreased C×43 mRNA and protein levels and GJIC activity. These suppressive effects, along with the induction of Smad1/5/8 phosphorylation, were attenuated by co-treatment with a BMP type I receptor inhibitor, dorsomorphin. Furthermore, knockdown of the central component of the transforming growth factor-β superfamily signaling pathway, Smad4, using small interfering RNA reversed the suppressive effects of BMP15 on C×43 expression and GJIC activity. The suppressive effects of BMP15 on C×43 expression were further confirmed in primary human granulosa-lutein cells obtained from infertile patients undergoing an in vitro fertilization procedure. These findings suggest that oocyte-derived BMP15 decreases GJIC activity between human granulosa cells by down-regulating C×43 expression, most likely via a Smad-dependent signaling pathway.
机译:在卵巢中,颗粒细胞中连接蛋白偶联的间隙连接在卵泡和卵母细胞的发育以及黄体的形成中起着至关重要的作用。我们以前的工作表明,caca细胞衍生的骨形态发生蛋白(BMP)4和BMP7通过下调永生化人类颗粒细胞中connexin43(C×43)的表达来降低间隙连接细胞间通讯(GJIC)的活性。然而,卵母细胞生长因子对C×43表达的影响尚待阐明。本研究旨在研究卵母细胞衍生的生长分化因子(GDF)9和BMP15对人颗粒细胞SVOG中C×43表达的影响。我们还检查了相对于GJIC活动的影响,并研究了潜在的作用机制。在SVOG细胞中,用BMP15而不是GDF9处理可显着降低C×43 mRNA和蛋白水平以及GJIC活性。这些抑制作用,以及Smad1 / 5/8磷酸化的诱导,通过与BMP I型受体抑制剂dorsomorphin共同处理而减弱。此外,使用小干扰RNA敲低转化生长因子-β超家族信号转导途径的核心成分Smad4,逆转了BMP15对C×43表达和GJIC活性的抑制作用。 BMP15对C×43表达的抑制作用在从接受体外受精程序的不育患者获得的原代人颗粒叶黄素细胞中得到了进一步证实。这些发现表明,卵母细胞衍生的BMP15通过下调C×43表达而降低了人类颗粒细胞之间的GJIC活性,这很可能是通过Smad依赖性信号通路。

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