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减数分裂阻滞前后的牛卵母细胞玻璃化:对超微结构和发育能力的影响。

Bovine oocyte vitrification before or after meiotic arrest: effects on ultrastructure and developmental ability.

作者信息

Diez Carmen, Duque Paloma, Gómez Enrique, Hidalgo Carlos O, Tamargo Carolina, Rodríguez Aida, Fernández Lina, de la Varga Santiago, Fernández Alba, Facal Nieves, Carbajo Maite

机构信息

Servicio Regional de Investigación y Desarrollo Agroalimentario, Camino de los Claveles 604, Somio, 33203 Gijón, Asturias, Spain.

出版信息

Theriogenology. 2005 Jul 15;64(2):317-33. doi: 10.1016/j.theriogenology.2004.11.023. Epub 2005 Jan 13.

Abstract

The nuclear stage at which oocytes are cryopreserved influences further development ability and cryopreservation affects ultrastructure of both cumulus cells and the oocyte. In this work, we analyze the effects of vitrification at different nuclear and cytoplasmic maturation stages on the oocyte ultrastructure and developmental ability. Culture in TCM199 + PVA with roscovitine 25 M during 24h led to meiotic arrest (MA) in cumulus-oocyte complexes (COCs), while permissive in vitro maturation (IVM) was performed in TCM199, 10% FCS, FSH-LH and 17beta-estradiol for 24 h. Oocytes were vitrified using the open pulled straw method (OPS) with minor modifications. Fresh and vitrified/warmed COCs were fixed as immature, after IVM, after meiotic arrest (MA) and after MA + IVM. Vitrification combined with MA followed by IVM produced the highest rates of degeneration, regardless of the vitrification time. As a consequence, lower proportions of embryos cleaved in these groups, although differences were eliminated at the five-eight cell stage. Development rates up to day 8 were similar in all experimental groups, being significantly lower than those in fresh controls. Only oocytes vitrified after IVM were able to give blastociysts. The morphological alterations observed can be responsible for compromised development. More research is needed to explain the low survival rates of the bovine oocyte after vitrification and warming.

摘要

卵母细胞冷冻保存时所处的核阶段会影响其进一步发育的能力,并且冷冻保存会影响卵丘细胞和卵母细胞的超微结构。在本研究中,我们分析了不同核成熟和胞质成熟阶段的玻璃化对卵母细胞超微结构和发育能力的影响。在含有25 μM 罗哌卡因的TCM199 + PVA中培养24小时可导致卵丘 - 卵母细胞复合体(COC)减数分裂停滞(MA),而在含有10%胎牛血清、促卵泡激素 - 促黄体生成素和17β - 雌二醇的TCM199中进行24小时的允许性体外成熟(IVM)。卵母细胞采用稍加修改的开放式拉管法(OPS)进行玻璃化。新鲜的以及玻璃化/复温后的COC在未成熟时、IVM后、减数分裂停滞(MA)后以及MA + IVM后进行固定。无论玻璃化时间如何,玻璃化结合MA后再进行IVM产生的退化率最高。因此,这些组中胚胎分裂的比例较低,尽管在5 - 8细胞阶段差异消失。所有实验组直至第8天的发育率相似,均显著低于新鲜对照组。只有IVM后玻璃化的卵母细胞能够发育成囊胚。观察到的形态学改变可能是发育受损的原因。需要更多研究来解释牛卵母细胞玻璃化和复温后的低存活率。

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