Suppr超能文献

用丁内酯I单独或与罗可辛联合使牛卵母细胞早熟后的核成熟动力学及体外胚胎发育

Nuclear maturation kinetics and in vitro embryo development of cattle oocytes prematured with butyrolactone I combined or not combined with roscovitine.

作者信息

Adona P R, Pires P R L, Quetglas M D, Schwarz K R L, Leal C L V

机构信息

ZAB, FZEA, USP, Pirassununga, SP, Brazil.

出版信息

Anim Reprod Sci. 2008 Mar 3;104(2-4):389-97. doi: 10.1016/j.anireprosci.2007.06.013. Epub 2007 Jun 15.

Abstract

Cyclin dependent kinase inhibitors (CDKIs) may be used for pre-maturation culture, but can accelerate nuclear maturation. The aim of the present research was to compare the effect of butyrolactone I (BLI) alone or combined with roscovitine (ROS) at lesser than typically used concentrations on nuclear maturation kinetics and embryo development. To assess maturation kinetics (Experiment 1), oocytes were cultured in 100 microM BLI (B) or 6.25 microM BLI+12.5 microM ROS (BR) in TCM-199 for 24 h. Oocytes were subsequently submitted to in vitro maturation (IVM) in TCM-199+0.5 microg/ml FSH, 50 microg/ml LH and 10% FCS for another 24 h, during which oocytes were fixed every 3 h. In Experiment 2, oocytes were submitted to 24h pre-maturation treatments, with the inhibitors being diluted in TCM-199 or DMEM. IVM lasted 21 h in the culture media DMEM+0.5 microg/ml FSH, 50 microg/ml LH, 5% FCS and 50 ng/ml EGF. After IVM, oocytes from all groups were fertilized in vitro. Oocytes and sperm (2x10(6) sperm cells/ml) were co-cultured for 18 h. Embryos were co-cultured with granulosa cells in CR2aa for 8 days. All cultures were in droplets under oil, at 38.5 degrees C and 5% CO2 in air. In both experiments, control oocytes (C) were submitted only to IVM. In Experiment 1, at 0 h, C and B oocytes were all (100%) at the germinal vesicle stage (GV) of development. BR had fewer GV oocytes (89%, P<0.05). After 3 h IVM, B and BR had fewer oocytes in GV (84.7 and 79.6%, P>0.05) than C (100%, P<0.05). At 12 h, most oocytes were at intermediate stages (metaphase to telophase I) in all groups (approximately 80%, P>0.05). After 21 (77-89%) and 24 h (85-95%), all groups had similar metaphase II (MII) rates of development (P>0.05). In Experiment 2, cleavage (79-84%, P>0.05) and Day 7 blastocyst rates (26-36%, P>0.05) were similar. After 8 days, the group pre-matured with BR in DMEM had lesser blastocyst rates of development (32.3%) lower than C (40.1%, P<0.05). The other groups were similar to C (35-38%, P>0.05). Hatching rates were similar (10-15%, P>0.05) as were total cell numbers (141-170). In conclusion, BR is less effective in maintaining meiosis block; B and BR accelerate meiosis resumption; and use of pre-maturation medium may affect developmental rates.

摘要

细胞周期蛋白依赖性激酶抑制剂(CDKIs)可用于提前成熟培养,但会加速核成熟。本研究的目的是比较单独使用丁内酯I(BLI)或与低于常用浓度的罗可辛(ROS)联合使用对核成熟动力学和胚胎发育的影响。为评估成熟动力学(实验1),将卵母细胞在含有100微摩尔BLI(B)或6.25微摩尔BLI + 12.5微摩尔ROS(BR)的TCM - 199中培养24小时。随后,卵母细胞在含有0.5微克/毫升促卵泡激素(FSH)、50微克/毫升促黄体生成素(LH)和10%胎牛血清(FCS)的TCM - 199中进行体外成熟(IVM)培养24小时,在此期间每3小时固定一次卵母细胞。在实验2中,卵母细胞进行24小时的提前成熟处理,抑制剂用TCM - 199或杜氏改良伊格尔培养基(DMEM)稀释。IVM在含有0.5微克/毫升FSH、50微克/毫升LH、5% FCS和50纳克/毫升表皮生长因子(EGF)的DMEM培养基中持续21小时。IVM后,所有组的卵母细胞进行体外受精。卵母细胞与精子(2×10⁶个精子细胞/毫升)共同培养18小时。胚胎与颗粒细胞在CR2aa培养基中共同培养8天。所有培养均在油滴中进行,温度为38.5℃,空气中二氧化碳浓度为5%。在两个实验中,对照卵母细胞(C)仅进行IVM。在实验1中,0小时时,C组和B组卵母细胞均处于发育的生发泡期(GV)(100%)。BR组的GV期卵母细胞较少(89%,P < 0.05)。IVM 3小时后,B组和BR组处于GV期的卵母细胞比C组少(分别为84.7%和79.6%,P > 0.05),C组为100%(P < 0.05)。12小时时,所有组大多数卵母细胞处于中间阶段(中期至末期I)(约80%,P > 0.05)。21小时(77 - 89%)和24小时(85 - 95%)后,所有组中期II(MII)期的发育率相似(P > 0.05)。在实验2中,卵裂率(79 - 84%,P > 0.05)和第7天囊胚率(26 - 36%,P > 0.05)相似。8天后,在DMEM中用BR提前成熟的组囊胚发育率较低(32.3%),低于C组(40.1%,P < 0.05)。其他组与C组相似(35 - 38%,P > 0.05)。孵化率相似(10 - 15%,P > 0.05),总细胞数也相似(141 - 170)。总之,BR在维持减数分裂阻滞方面效果较差;B和BR加速减数分裂恢复;提前成熟培养基的使用可能影响发育率。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验