对用于雌性配子卵巢内玻璃化的低温保护介质 compoud 进行现代化改造

Т. Kuzmina, D. Starikova
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引用次数: 0

摘要

目的对使用二甲基甘油酸硅(SDMG)进行卵巢内玻璃化处理的家猪体细胞(卵母细胞)和生殖细胞(卵细胞)的形态功能状态进行综合分析。将 15×20 mm 大小的猪卵巢片段(FsPO)逐渐保存在用含 20% 胎牛血清(FBS)的磷酸盐缓冲盐水(PBS)配制的冷冻保护剂(CPA)中:在 CPA-1 [7.5% EG(乙二醇)加 7.5% DMSO(二甲亚砜)] 中保存 25 分钟,在 CPA-2 [15% EG 加 15% DMSO 和 0.5 M 蔗糖] 中保存 15 分钟。通过添加 SDMG(浓度为 2%、6% 或 10%)改变了实验组中 CPA-2 的成分。FsPO 保存在液氮中。将 FsPO 在溶液 1(80% PBS、20% FBS、0.5 摩尔/升蔗糖)中暴露 1 分钟,在溶液 2(80% PBS、0.25 摩尔/升蔗糖)中暴露 5 分钟,使其脱冻。分析了脱盐的精原细胞-卵母细胞复合物(COCs)的抗冷冻性的以下指标:精原细胞扩张程度、卵母细胞形态和雌配子脂质体的功能状态(尼罗河红/脂滴复合物的荧光强度 - FILDs)。在低温保护介质中添加 SDMG 可降低玻璃化后卵母细胞的变性程度。在添加 10% SDMG 的实验组中,不同程度的积层细胞扩增(低、中、高)的配子水平趋向于原生细胞组的指标。有形态退化迹象的原生卵母细胞水平(7.7%)与 10% SDMG 的卵巢内玻璃化配子水平(11%)无显著差异。在对照组(16.5%)和添加了6% SDMG(4.8%)和10% SDMG(11.8%,P<0.001)的玻璃化卵母细胞中,FILDs较低的原生卵母细胞比例(38.9%)超过了具有上述指标的卵母细胞水平。总体而言,对进行卵巢内玻璃化的家猪COCs抗冷冻性指标的全面监测显示了SDMG的冷冻保护特性。其效果与剂量有关,表现为稳定卵母细胞与卵丘的交流、减少有形态退化迹象的卵母细胞数量,以及使用不同浓度的 SDMG 进行卵巢内玻璃化的雌配子的脂质体功能特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modernization of the cryoprotective medium compoud for intraovarian vitrification of female gametes of Sus scrofa domesticus
Aim. Comprehensive analysis of the morphofunctional state of somatic (cumulus) and germ cells (oocytes) of Sus scrofa domesticus subjected to intraovarian vitrification using silicon dimethylglycerolate (SDMG) are presented.Materials and methods. Fragments of porcine ovaries (FsPO) 15×20 mm in size were gradually kept in cryoprotective agents (CPA) prepared in phosphate-buffered saline (PBS) with 20% fetal bovine serum (FBS): 25 min. in CPA-1 [7.5 % EG (ethylene glycol) with 7.5 % DMSO (dimethyl sulfoxide)] and 15 min. in CPA-2 (15 % EG with 15 % DMSO and 0.5 M sucrose). The composition of the CPA-2 in experimental groups was modified by addition of SDMG (at concentrations of 2 %, 6 %, or 10 %). FsPO were stored in liquid nitrogen. FsPO were devitrified by exposure 1 minute in solution 1 (80 % PBS, 20 % FBS, 0.5 mol/l sucrose) and 5 minutes in solution 2 (80 % PBS, 0.25 mol/l sucrose). The following indicators of cryoresistance of devitrified cumulus-oocyte complexes (COCs) were analyzed: degree of cumulus cells expansion; oocyte morphology and the functional status of lipidome in female gametes (fluorescence intensity of Nile red /lipid droplets complex - FILDs).Results. The addition of SDMG into cryoprotective media reduced the level of denuded oocytes after vitrification. The level of gamete with different degree of cumulus cells expansion (low, medium, high) in the experimental group with 10 % SDMG tended to indicators in the group of native cells. The level of native oocytes with the signs of morphological degeneration (7.7%) had no significant differences with the level of intraovarian vitrified gametes with 10 % SDMG (11 %). The proportion of native oocytes with low FILDs (38.9 %) exceeded the level of oocytes with the above indicator in vitrified oocytes of the control (16.5 %) group and in experimental groups of cells with the addition of 6 % SDMG (4.8 %) and 10 % SDMG (11.8 %, P<0.001).Conclusion. In general, comprehensive monitoring of indicators cryoresistance of COCs in Sus scrofa domesticus subjected to intraovarian vitrification revealed the cryoprotective properties of SDMG. The effects were dose-dependent and were expressed in the stabilization of oocyte-cumulus communication, a decrease in the level of oocytes with the signs of morphological degeneration, and features of the lipidome functioning in intraovarian vitrified female gametes using SDMG at various concentrations.
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