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Roles of epidermal growth factor (EGF)‐like factor in the ovulation process

机译:表皮生长因子(EGF)样因子在排卵过程中的作用

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摘要

Luteinizing hormone (LH) surge stimulates preovulatory follicles to induce the ovulation process, including oocyte maturation, cumulus expansion, and granulosa cell luteinization. The matured oocytes surrounded by an expanded cumulus cell layer are released from follicles to the oviduct. However, LH receptors are dominantly expressed in granulosa cells, but less in cumulus cells and are not expressed in oocytes, indicating that the secondary factors expressed and secreted from LH‐stimulated granulosa cells are required for the induction of the ovulation process. Prostaglandin and progesterone are well‐known factors that are produced in granulosa cells and then stimulate in both granulosa and cumulus cells. The mutant mice of prostaglandin synthase (Ptgs2KO mice) or progesterone receptor (PRKO mice) revealed that the functions were essential to accomplish the ovulation process, but not to induce the ovulation process. To identify the factors initiating the transfer of the stimuli of LH surge from granulosa cells to cumulus cells, M. Conti's lab and our group performed microarray analysis of granulosa cells and identified the epidermal growth factor (EGF)‐like factor, amphiregulin (AREG), epiregulin (EREG), and β‐cellulin (BTC) that act on EGF receptor (EGFR) and then induce the ERK1/2 and Ca2+‐PLC pathways in cumulus cells. When each of the pathways was down‐regulated using a pharmacological approach or gene targeting study, the induction of cumulus expansion and oocyte maturation were dramatically suppressed, indicating that both pathways are inducers of the ovulation process. However, an in vitro culture study also revealed that the EGFR‐induced unphysiological activation of PKC in cumulus cells accelerated oocyte maturation with low cytostatic activity. Thus, the matured oocytes are not arrested at the metaphase II (MII) stage and then spontaneously form pronuclei. The expression of another type of EGF‐like factor, neuregulin 1 (NRG1), that does not act on EGFR, but selectively binds to ErbB3 is observed in granulosa cells after the LH surge. NRG1 supports EGFR‐induced ERK1/2 phosphorylation, but reduces PKC activity to physiological level in the cumulus cells, which delays the timing of meiotic maturation of oocytes to adjust the timing of ovulation. Thus, both types of EGF‐like factor are rapidly induced by LH surge and then stimulate cumulus cells to control ERK1/2 and PKC pathways, which results in the release of matured oocytes with a fertilization competence.
机译:黄体生成素(LH)激增刺激排卵前卵泡诱导排卵过程,包括卵母细胞成熟,卵丘膨胀和颗粒细胞黄体化。被扩大的卵丘细胞层围绕的成熟卵母细胞从卵泡释放到输卵管。但是,LH受体主要在颗粒细胞中表达,而在卵丘细胞中较少表达,而在卵母细胞中不表达,表明诱导LH刺激的颗粒细胞表达和分泌的次级因子是诱导排卵过程所必需的。前列腺素和孕酮是在颗粒细胞中产生并随后在颗粒细胞和卵丘细胞中刺激的众所周知的因子。前列腺素合酶的突变小鼠(Ptgs2KO小鼠)或孕激素受体(PRKO小鼠)显示,这些功能对于完成排卵过程至关重要,但不能诱导排卵过程。为了确定启动LH刺激刺激从颗粒细胞转移到卵丘细胞的因素,M。Conti的实验室和我们的小组对颗粒细胞进行了微阵列分析,并鉴定了表皮生长因子(EGF)样因子两性调节蛋白(AREG) ,上皮调节蛋白(EREG)和β-纤维蛋白(BTC)作用于EGF受体(EGFR),然后在卵丘细胞中诱导ERK1 / 2和Ca 2 + -PLC途径。当使用药理学方法或基因靶向研究下调每种途径时,显着抑制了卵丘扩张和卵母细胞成熟的诱导,表明这两种途径都是排卵过程的诱导剂。但是,一项体外培养研究还显示,EGFR诱导卵丘细胞中PKC的非生理激活会加速卵母细胞的成熟,但抑制细胞活性却较低。因此,成熟的卵母细胞不会停留在中期II(MII)阶段,然后自发形成原核。 LH激增后,在颗粒细胞中观察到另一类EGF样因子神经调节蛋白1(NRG1)的表达不作用于EGFR,但选择性结合ErbB3。 NRG1支持EGFR诱导的ERK1 / 2磷酸化,但可将卵丘细胞的PKC活性降低至生理水平,从而延迟了卵母细胞减数分裂成熟的时间,以调节排卵的时间。因此,两种类型的EGF样因子都被LH激增迅速诱导,然后刺激卵丘细胞控制ERK1 / 2和PKC途径,从而释放具有受精能力的成熟卵母细胞。

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