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当前位置: 首页 > 文章 > An efficient method for the sanitary vitrification of bovine oocytes in straws 畜牧与生物技术杂志(英文版) 2014,5 (4) 399-405
Position: Home > Articles > An efficient method for the sanitary vitrification of bovine oocytes in straws Journal of Animal Science and Biotechnology 2014,5 (4) 399-405

An efficient method for the sanitary vitrification of bovine oocytes in straws

作  者：
Yanhua Zhou;Xiangwei Fu;Guangbin Zhou;Baoyu Jia;Y. Fang;Yunpeng Hou;Shi-En Zh
单  位：
National Engineering Laboratory for Animal Breeding, Key Laboratory of Animal genetics, Breeding and Reproduction, Ministry of Agriculture, College of Animal Science and Technology, China Agricultural University, Beijing, P.R. China;Institute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural University (Chengdu Campus), Wenjiang, P.R. China;State Key Laboratory for Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing, P.R. China;National Engineering Laboratory for Animal Breeding, Key Laboratory of Animal genetics, Breeding and Reproduction, Ministry of Agriculture, College of Animal Science and Technology, China Agricultural University, Beijing, P.R. Chin
关键词：
Bovine;Cryopreservation;Oocytes;Straw;Vitrificatio
摘  要：
Background: At present, vitrification has been widely applied to humans, mice and farm animals. To improve the efficiency of vitrification in straw, bovine oocytes were used to test a new two-step vitrification method in this study.Results: When in vitro matured oocytes were exposed to 20% ethylene glycol (EG20) for 5 min and 40% ethylene glycol (EG40) for 30 s, followed by treatment with 30% glycerol (Gly30), Gly40 or Gly50, a volume expansion was observed in Gly30 and Gly40 but not Gly50. This indicates that the intracellular osmotic pressure after a 30 s differs between EG40 and ranged between Gly40 (approximately 5.6 mol/L) and Gly50 (approximately 7.0 mol/L). Since oocytes are in EG40 just for only a short period of time (30s) and at a lower temperature (4°C), we hypothesize that the main function of this step in to induce dehydration. Based on these results, we omitted the EG40 step, before oocytes were pretreated in EG20 for 5 min, exposed to pre-cooled (4°C) Gly50, for30 s, and then dipped into liquid nitrogen. After warming, 81.1% of the oocytes survived, and the surviving oocytes developed into cleavage stage embryos (63.5%) or blastocysts (20.0%) after parthenogenetic activation.Conclusions: These results demonstrate that in a two-step vitrification procedure, the permeability effect in the second step is not necessary. It is possible that the second step is only required to provide adequate osmotic pressure to condense the intracellular concentration of CPAs to a level required for successful vitrification.

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