首页> 外文期刊>Molecular and Cellular Endocrinology >Meiosis activating sterol (MAS) regulate FSH-induced meiotic resumption of cumulus cell-enclosed porcine oocytes via PKC pathway.
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Meiosis activating sterol (MAS) regulate FSH-induced meiotic resumption of cumulus cell-enclosed porcine oocytes via PKC pathway.

机译:减数分裂激活固醇(MAS)通过PKC途径调节FSH诱导的卵丘细胞封闭的猪卵母细胞的减数分裂恢复。

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摘要

Meiosis activating sterol (MAS) have been found to be able to promote oocytes meiotic maturation of small animals in vitro, such as mouse, rat and rabbit. But in large animals, whether MAS play the same function, especially the physiological mechanisms of MAS on oocytes maturation are not clear. To our knowledge, this is the first time to investigate the role and signal pathway of MAS on FSH-induced porcine oocytes meiotic resumption. Porcine cumulus-enclosed oocytes (CEOs) isolated from 3 to 5mm follicles were cultured in the FSH-medium for 24h supplemented with 0-50 microM RS21745 or 0-100 microM RS21607 (two specific inhibitors of lanosterol 14alpha-demethylase that converts lanosterol to FF-MAS), or cultured in FSH-medium with 25 microM RS21745 for 0-24h firstly, then transferred into a new FSH-medium (the total culture time is 24h). The results revealed that RS21745 or RS21607 could inhibit FSH-induced porcine CEOs meiotic resumption in a dose and time-dependent manner. Meanwhile, FSH-induced cumulus expansion could also be inhibited dose-dependently by RS21745 or RS21607. Otherwise, AY9944-A-7, an inhibitor of Delta14-reductase which promotes cholesterol accumulation from FF-MAS, had no effect on both denuded oocytes (DOs) cultured for 24 or 44 h and CEOs cultured for 24h meiotic resumption, but it could promote CEOs meiotic resumption after 44 h culture. In addition, we got that 10(-8) to 10(-6)M PMA, an activator of PKC pathway, could reverse the inhibiting effect of RS21745 on FSH-induced CEOs meiotic resumption and enhance the rate of germinal vesicle breakdown (GVBD) of CEOs cultured in medium with hypoxanthine (HX). Moreover, 5-10 microM chelerythrine chloride, an inhibitor of PKC, could enhance the inhibitory effect of RS21745 on FSH-induced porcine oocytes resumption of meiosis. All the data of this study support that endogenous FF-MAS takes part in the FSH-induced porcine oocytes meiotic resumption and might play an active role via PKC signal pathway.
机译:已经发现减数分裂活化固醇(MAS)能够在体外促进小动物如小鼠,大鼠和兔子的卵母细胞减数分裂成熟。但是在大型动物中,MAS是否发挥相同的功能,尤其是MAS对卵母细胞成熟的生理机制尚不清楚。据我们所知,这是首次研究MAS在FSH诱导的猪卵母细胞减数分裂恢复中的作用和信号途径。在3至5毫米卵泡中分离的猪卵丘封闭卵母细胞(CEOs)在FSH培养基中培养24小时,并补充0-50 microM RS21745或0-100 microM RS21607(两种将羊毛甾醇转化为FF的羊毛甾醇14α-脱甲基酶的特异性抑制剂-MAS),或先在含有25 microM RS21745的FSH培养基中培养0-24h,然后转移到新的FSH培养基中(总培养时间为24h)。结果表明,RS21745或RS21607可以抑制FSH诱导的猪CEOs减数分裂的恢复,且呈剂量和时间依赖性。同时,RS21745或RS21607也可以剂量依赖性地抑制FSH诱导的积云扩张。否则,AY9944-A-7(一种可促进FF-MAS积累胆固醇的Delta14-还原酶抑制剂)对培养24或44 h的裸露卵母细胞(DOs)和培养24h减数分裂恢复的CEO均无影响,但它可以培养44 h后促进CEO减数分裂的恢复。此外,我们发现PKC途径的激活剂10(-8)至10(-6)M PMA可以逆转RS21745对FSH诱导的CEO减数分裂恢复的抑制作用,并提高发芽囊泡分解率(GVBD) )在含有次黄嘌呤(HX)的培养基中培养的CEO。此外,PKC抑制剂5-10 microM白屈菜红碱氯化物可以增强RS21745对FSH诱导的猪卵母细胞减数分裂恢复的抑制作用。这项研究的所有数据都支持内源性FF-MAS参与FSH诱导的猪卵母细胞减数分裂恢复,并可能通过PKC信号通路发挥积极作用。

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