首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >A negative feedback system between oocyte bone morphogenetic protein 15 and granulosa cell kit ligand: Its role in regulating granulosa cell mitosis
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A negative feedback system between oocyte bone morphogenetic protein 15 and granulosa cell kit ligand: Its role in regulating granulosa cell mitosis

机译:卵母细胞骨形态发生蛋白15与颗粒细胞试剂盒配体之间的负反馈系统:在调节颗粒细胞有丝分裂中的作用

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摘要

Although the existence of a regulatory paracrine feedback system between oocytes and follicular somatic cells has been postulated for some time, there has not yet been any definitive evidence that such a communication system exists. Herein we present a previously undescribed oocyte-granulosa cell (GC) feedback communication system involving an oocyte-derived factor, bone morphogenetic protein-15 (BMP-15) and a GC-derived factor, kit ligand (KL), both of which have been shown to be crucial regulators of female reproduction. We used a coculture system of rat oocytes and GCs and found that BMP-15 stimulates KL expression in GCs, whereas KL inhibits BMP-15 expression in oocytes, thus forming a negative feedback loop. Moreover, KL, like BMP-15, exhibited mitotic activity on GCs in the presence of oocytes. Because c-kit (KL receptor) is expressed in oocytes but not GCs, the oocytes must be involved in mediating the KL-induced GC mitosis. Furthermore, the blockage of c-kit signaling in oocytes by using a c-kit neutralizing antibody markedly suppressed BMP-15-induced GC mitosis, suggesting that the oocyte must play a role in the GC responses to BMP-15. In contrast, the c-kit antibody had no effect on the mitotic activities of two other known GC mitogens, activin-A and BMP-7. Altogether, this study presents direct evidence of a negative feedback system governed by oocyte-derived BMP-15 and GC-derived KL, and demonstrates that the mitotic activities of BMP-15 and KL for GCs depend on this oocyte–GC communication system. We hypothesize that the negative feedback system most likely plays a pivotal role in early folliculogenesis.
机译:尽管已经假定卵母细胞和滤泡性体细胞之间存在调节旁分泌反馈系统已有一段时间,但尚无任何确凿的证据表明存在这种通讯系统。本文中,我们介绍了一个先前未描述的卵母细胞-颗粒细胞(GC)反馈通信系统,该系统涉及卵母细胞衍生因子,骨形态发生蛋白-15(BMP-15)和GC衍生因子,试剂盒配体(KL),两者均具有被证明是女性生殖的关键调节器。我们使用了大鼠卵母细胞和GC的共培养系统,发现BMP-15刺激了GC中的KL表达,而KL抑制了卵母细胞中BMP-15的表达,从而形成了负反馈回路。此外,在卵母细胞存在下,KL与BMP-15一样,对GC表现出有丝分裂活性。因为c-kit(KL受体)在卵母细胞中表达但在GC中不表达,所以卵母细胞必须参与介导KL诱导的GC有丝分裂。此外,通过使用c-kit中和抗体阻断卵母细胞中c-kit信号传导,可显着抑制BMP-15诱导的GC有丝分裂,提示卵母细胞必须在对BMP-15的GC反应中发挥作用。相反,c-kit抗体对另外两种已知的GC丝裂原,激活素A和BMP-7的有丝分裂活性没有影响。总而言之,这项研究提供了直接反馈证据,表明负反馈系统受卵母细胞衍生的BMP-15和GC衍生的KL的支配,并证明BMP-15和KL对GC的有丝分裂活性取决于卵母细胞与GC的通讯系统。我们假设负反馈系统很可能在早期卵泡形成中起关键作用。

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