首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cyclic AMP-mediated control of meiosis: effects of progesterone cholera toxin and membrane-active drugs in Xenopus laevis oocytes.
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Cyclic AMP-mediated control of meiosis: effects of progesterone cholera toxin and membrane-active drugs in Xenopus laevis oocytes.

机译:环AMP介导的减数分裂控制:非洲爪蟾卵母细胞中的孕酮霍乱毒素和膜活性药物的作用。

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摘要

Progesterone depressed rapidly (50% at 1 min) and persistently cyclic AMP (cAMP) concentration that had been elevated by cholera toxin in Xenopus laevis oocytes. cAMP remained below 1 pmol per oocyte (mean basal level) for approximately 1 hr and thereafter rose to approximately 120% of control values, while germinal vesicle (nucleus) breakdown did not occur. In the absence of cholera toxin, progesterone treatment for 6 hr maintained cAMP concentration below the basal level (but not lower than 80%), and germinal vesicle breakdown occurred. Experiments in the presence of phosphodiesterase inhibitors suggested that progesterone modulates adenylate cyclase activity. The maturation promoting factor, which is formed after 3-5 hr of progesterone treatment and provokes germinal vesicle breakdown after its injection into untreated oocytes, also decreased cAMP concentration, an observation that may explain its "autoamplification." Nonsteroidal inducers of meiosis reinitiation (e.g., propranolol, methoxyverapamil, mersalyl) diminished the cholera toxin-mediated accumulation of cAMP, in contrast to compounds devoid of meiotic-inducing capacity and antagonist to progesterone action, such as gammexane (an inositol analogue) and 5'-deoxy-S-(2-methylpropyl)-5'-thioadenosine (a methylase inhibitor), that increased the nucleotide level. The fine control, suggested by the effects of small changes in cAMP levels, gives evidence of great sensitivity to a critical determinant governing meiotic cell division.
机译:在非洲爪蟾卵母细胞中,黄体酮迅速降低(在1分钟时占50%),并持续引起环内AMP(cAMP)浓度升高,此浓度已由霍乱毒素升高。 cAMP在每个卵母细胞中均保持低于1 pmol(平均基础水平)的状态持续约1个小时,此后上升至对照值的约120%,而未发生生小泡(细胞核)分解。在没有霍乱毒素的情况下,黄体酮治疗6小时可将cAMP浓度维持在基础水平以下(但不低于80%),并且发生生小泡破裂。在磷酸二酯酶抑制剂存在下的实验表明,孕酮调节腺苷酸环化酶活性。促孕因子在孕激素处理3-5小时后形成,并在将其注入未经处理的卵母细胞后引起发芽囊泡破裂,它的cAMP浓度也降低了,这一观察结果可以解释其“自动扩增”的原因。非甾体减数分裂重新诱导剂(如普萘洛尔,甲氧基维拉帕米,美沙拉利)减少了霍乱毒素介导的cAMP的积累,与缺乏减数分裂诱导能力和孕激素作用的拮抗剂的化合物(例如,gammexane(肌醇类似物)和5)相反'-脱氧-S-(2-甲基丙基)-5'-硫代腺苷(一种甲基化酶抑制剂),可增加核苷酸水平。由cAMP水平微小变化的影响提示的精细控制,对控制减数分裂细胞分裂的关键决定因素具有很高的敏感性。

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