减数分裂激活甾醇(MAS)与哺乳动物和人的生育。

Journal of Experimental Zoology Pub Date : 1999-10-15
A G Byskov, C Y Andersen, L Leonardsen, M Baltsen
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引用次数: 0

摘要

在哺乳动物中,已经发现两种减数分裂激活甾醇(MAS)在体外激活小鼠卵母细胞的减数分裂恢复。FF-MAS(4,4 -二甲基-5 - α -胆碱-8,14,24-三烯-3 - β -醇)从人排卵前卵泡液中提取,T-MAS(4,4 -二甲基-5 - α -胆碱-8,24-二烯-3 - β -醇)从公牛睾丸组织中提取。出乎意料的是,这两种从羊毛甾醇引入胆固醇生物合成途径的甾醇可能是对生殖具有重要生理功能的局部作用物质。FF-MAS和T-MAS存在于不同哺乳动物的排卵前卵泡液中,并且在次黄嘌呤(一种天然减数分裂成熟抑制剂)存在下培养的小鼠卵母细胞中具有启动减数分裂恢复的能力。FF-MAS是由完整卵丘-卵丘复合物的卵丘细胞在fsh刺激下产生的,为卵母细胞恢复减数分裂提供了一个启动信号。在哺乳动物睾丸和人类射精中发现的MAS中,T-MAS占绝大多数;特别是在精子中发现了高浓度。T-MAS可能由精子产生,精子中T-MAS的存在可能表明T-MAS通过影响第二次减数分裂来参与受精。Exp。黑旋风。(Mol. Dev. evolution .) 285:237-242, 1999。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meiosis activating sterols (MAS) and fertility in mammals and man.

In mammals two meiosis activating sterols (MAS) have been found to activate meiotic resumption in mouse oocytes, in vitro. FF-MAS (4, 4-dimethyl-5alpha-cholesta-8,14,24-triene-3beta-ol) was extracted from human preovulatory follicular fluid and T-MAS (4, 4-dimethyl-5alpha-cholest-8,24-diene-3beta-ol) from bull testicular tissue. Quite unexpected, these two sterols, which introduce the cholesterol biosynthetic pathway from lanosterol, may be locally acting substances with important physiological function for reproduction. FF-MAS and T-MAS are present in the preovulatory follicular fluid of different mammalian species and have the capacity to initiate resumption of meiosis in mouse oocyte cultured in the presence of hypoxanthine, a natural meiosis maturation inhibitor. FF-MAS is produced by the cumulus cells of intact oocyte-cumulus complexes upon FSH-stimulation and provides the oocyte with a go-signal for the resumption of meiosis. T-MAS constitutes the vast majority of MAS found in the mammalian testis and in the human ejaculate; in particular a high concentration is found in the spermatozoa. T-MAS may be produced by the spermatids and the presence of T-MAS in spermatozoa may suggest that T-MAS plays a role in fertilization by affecting the second meiotic division.J. Exp. Zool. (Mol. Dev. Evol.) 285:237-242, 1999.

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