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Ultrastructural characterization of fresh and cryopreserved in vivo produced ovine embryos

机译:新鲜和冷冻保存的体内产生的绵羊胚胎的超微结构表征

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Controlled slow freezing and vitrification have been successfully used for ovine embryo cryopreservation. Selection of embryos for transfer is based on stereomicroscopical embryo scoring after thawing, but the subjectivity inherent to this selection step has been demonstrated by ultrastructural studies of controlled slow frozen, in vivo produced ovine morulae and blastocysts. These studies have shown that certain abnormalities remain undetected by stereomicroscopy only. In the present study, using ovine in vivo produced morulae and blastocysts, we have studied the ultrastructural alterations induced by open pulled straw vitrification (OPS) and controlled slow freezing, compared stereomicroscopical embryo scoring with light microscopy evaluation of embryo's semithin sections, and related the ultrastructural cellular damage with the embryo classification by stereomicroscopical embryo scoring of embryos' and semithin section evaluation by light microscopy. The ultrastructural lesions found for OPS-vitrified and controlled slow frozen embryos were similar, independently of embryo stage. A significant higher number of grade 3 embryos was found at stereomicroscopical scoring after controlled slow freezing (P =0.02), and a significant higher number of grade 3 blastocysts was found at semithin sectioning after OPS vitrification (P =0.037). The extension of ultrastructural damage, especially of mitochondria and cytoskeleton, was related to the semithin classification but not to stereomicroscopical scoring at thawing. This suggests that semithin scoring is a useful tool for predicting ultrastructural lesions and new improvements in cryopreservation and thawing methods of ovine embryos are still warranted, including in the case of blastocysts cryopreserved by OPS vitrification.
机译:控制缓慢冷冻和玻璃化已成功用于绵羊胚胎的冷冻保存。移植后胚胎的选择基于解冻后的立体显微镜胚胎评分,但是通过控制缓慢冷冻,体内产生的绵羊桑ula和胚泡的超微结构研究已证明了该选择步骤固有的主观性。这些研究表明,仅通过立体显微镜仍无法检测到某些异常。在本研究中,我们使用绵羊体内产生的桑ula和胚泡,研究了开放式拉管玻璃化(OPS)和受控缓慢冷冻诱导的超微结构改变,将体视显微镜下的胚胎评分与光学显微镜评估的胚胎半薄切片进行了比较,并与超微结构细胞损伤,通过立体显微镜对胚胎进行评分,对胚胎进行分类,并通过光学显微镜评估半薄切片。 OPS玻璃化和受控的慢速冷冻胚胎的超微结构损害相似,与胚胎阶段无关。在控制缓慢冷冻后,通过立体显微镜评分,发现大量较高的3级胚胎(P = 0.02),在OPS玻璃化后的半薄切片中发现大量较高的3级胚泡(P = 0.037)。超微结构损伤的扩展,特别是线粒体和细胞骨架的扩展,与半薄分类有关,但与解冻时的立体显微镜评分无关。这表明,半薄评分是预测超微结构病变的有用工具,并且仍然需要对绵羊胚胎的冷冻保存和融化方法进行新的改进,包括在通过OPS玻璃化冷冻保存的囊胚的情况下。

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