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高 cGMP 和低 PDE3A 活性与卵母细胞减数分裂无能有关。

High cGMP and low PDE3A activity are associated with oocyte meiotic incompetence.

机构信息

Department of Ruminant Science, Agricultural Research Organization , Bet Dagan , Israel.

Department of Biological Regulation, Weizmann Institute of Science , Rehovot , Israel.

出版信息

Cell Cycle. 2019 Oct;18(20):2629-2640. doi: 10.1080/15384101.2019.1652472. Epub 2019 Aug 12.

Abstract

Resumption of meiosis in mammalian oocytes, defined as oocyte maturation, is stimulated by luteinizing hormone (LH). Fully grown oocytes can also mature spontaneously, upon their release from the ovarian follicle. However, growing oocytes fail to resume meiosis and the mechanism underlying their meiotic incompetence is unknown. It is commonly accepted that a drop in intraoocyte cyclic guanosine monophosphate (cGMP) resulting in the elevated activity of the oocyte-specific PDE3A leads to a decrease in cAMP content, essential for reinitiation of meiosis. We explored the regulation of these cyclic nucleotides and their degrading PDE3A in growing oocytes. Our research addressed the LH-induced rather than spontaneous oocyte maturation. We examined 16-21 as compared to 25-day-old, PMSG-primed rats, treated with the LH analog, hCG. The effect of LH was also examined , in isolated ovarian follicles. We found that hCG failed to induce oocyte maturation and ovulation in the younger animals and that ovulation-associated genes were not upregulated in response to this gonadotropin. Furthemore, the drop of intraoocyte cGMP and cAMP observed in fully grown oocytes upon exposure of the ovary to LH, was not detected in growing oocytes. Interestingly, whereas the global expression of PDE3A in growing and fully grown oocytes is similar, a significantly lower activity of this enzyme was determined in growing oocytes. Our findings show that meiotic incompetence is associated with a relatively high oocyte cGMP concentration and a low activity of PDE3A, which in follicle-enclosed oocytes may represent the failure of the somatic follicle cells to respond to LH.

摘要

哺乳动物卵母细胞减数分裂的恢复(定义为卵母细胞成熟)受黄体生成素(LH)刺激。完全生长的卵母细胞也可以自发成熟,从卵巢滤泡中释放出来。然而,生长中的卵母细胞不能恢复减数分裂,其减数分裂无能的机制尚不清楚。通常认为,卵母细胞内环鸟苷单磷酸(cGMP)的下降导致卵母细胞特异性 PDE3A 的活性升高,从而导致 cAMP 含量减少,这对于重新启动减数分裂是必不可少的。我们探索了这些环核苷酸及其降解 PDE3A 在生长中的卵母细胞中的调节。我们的研究针对的是 LH 诱导的而不是自发的卵母细胞成熟。我们检查了 16-21 天龄与 25 天龄的 PMSG 诱导的大鼠,并用 LH 类似物 hCG 处理。还检查了 LH 对分离的卵巢滤泡的影响。我们发现,hCG 不能在年轻动物中诱导卵母细胞成熟和排卵,并且这种促性腺激素没有上调排卵相关基因。此外,在将卵巢暴露于 LH 后,在完全生长的卵母细胞中观察到的卵内 cGMP 和 cAMP 的下降,在生长中的卵母细胞中未检测到。有趣的是,尽管生长中和完全生长的卵母细胞中的 PDE3A 总体表达相似,但在生长中的卵母细胞中测定的这种酶的活性明显较低。我们的研究结果表明,减数分裂无能与卵母细胞中相对较高的 cGMP 浓度和 PDE3A 活性降低有关,在滤泡封闭的卵母细胞中,这可能代表体腔滤泡细胞对 LH 反应失败。

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