Department of Pathology and Veterinary Clinics, University of Sassari, Via Vienna 2, 07100 Sassari, Italy.
Cryobiology. 2012 Jun;64(3):267-72. doi: 10.1016/j.cryobiol.2012.02.010. Epub 2012 Feb 22.
Cryopreservation-induced modifications of zona pellucida (ZP) have been explored to a lesser extent compared to other oocyte compartments. Different methods have been applied to identify ZP changes, but most of them are invasive and measure only few properties of ZP. Raman microspectroscopy (RMS) is a powerful technique for studying the molecular composition of cells but to date few studies have been performed on the oocytes using this method. The aim of the present study is to investigate the structural modifications of ZP of vitrified/warmed in vitro matured ovine oocytes by means of RMS. Cumulus-oocyte complexes were recovered from the ovaries of slaughtered adult sheep, matured in vitro and vitrified following the Minimum Essential Volume method using cryotops. ZPs of vitrified/warmed oocytes (VITRI), were exposed to vitrification solutions but not cryopreserved (CPA-exp) and untreated oocytes (CTR) were analyzed by RMS. We focused our analysis on the ZP protein and carbohydrate components by analyzing the 1230-1300 cm(-1) amide III region and the 1020-1140 cm(-1) spectral range in RMS spectra, respectively. The spectral profiles in the ranges of proteins and carbohydrates were comparable between CTR and CPA-exp ZPs, whereas VITRI ZPs showed a significantly altered protein secondary structure characterized by an increase in β-sheet content and a decrease in the α-helix content. A significant modification of the carbohydrate components was also observed. This study demonstrates that vitrification of ovine oocytes induces biochemical changes of ZP related to the secondary structure of proteins and carbohydrate residues. Cryoprotectants do not strongly alter the molecular composition of ZP which is affected mainly by cooling. Raman technology offers a powerful and non-invasive tool to assess molecular modifications induced by cryopreservation in oocytes.
与其他卵母细胞隔室相比,对透明带(ZP)的冷冻保存诱导的修饰的研究较少。已经应用了不同的方法来识别 ZP 变化,但它们大多数是侵入性的,并且仅测量 ZP 的少数几个特性。拉曼微光谱(RMS)是研究细胞分子组成的强大技术,但迄今为止,使用这种方法对卵母细胞进行的研究很少。本研究的目的是通过 RMS 研究玻璃化/解冻的体外成熟绵羊卵母细胞的 ZP 结构修饰。从屠宰成年绵羊的卵巢中回收卵丘-卵母细胞复合物,在体外成熟,并使用 cryotops 采用最小必需体积方法进行玻璃化。玻璃化/解冻的卵母细胞(VITRI)的 ZP 暴露于玻璃化溶液中但未进行冷冻保存(CPA-exp),并且未处理的卵母细胞(CTR)通过 RMS 进行分析。我们通过分析 RMS 光谱中分别为 1230-1300 cm(-1)酰胺 III 区域和 1020-1140 cm(-1)光谱范围,重点分析了 ZP 蛋白和碳水化合物成分。在 CTR 和 CPA-exp ZP 之间,蛋白质和碳水化合物范围的光谱谱线相似,而 VITRI ZP 显示出蛋白质二级结构的明显改变,其特征在于β-折叠含量增加和α-螺旋含量减少。还观察到碳水化合物成分的显着修饰。这项研究表明,绵羊卵母细胞的玻璃化诱导与蛋白质和碳水化合物残基的二级结构相关的 ZP 生化变化。冷冻保护剂不会强烈改变 ZP 的分子组成,主要受冷却影响。拉曼技术提供了一种强大的非侵入性工具,可用于评估卵母细胞冷冻保存引起的分子变化。