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两种玻璃化胚胎冷冻方法对不同品系小鼠胚胎冷冻效果比较
引用本文:王俊风,李淼,张艺宝,郁丽丽,魏勤,刘丽均,施美莲,徐平.两种玻璃化胚胎冷冻方法对不同品系小鼠胚胎冷冻效果比较[J].中国实验动物学杂志,2013(6):12-15.
作者姓名:王俊风  李淼  张艺宝  郁丽丽  魏勤  刘丽均  施美莲  徐平
作者单位:[1]上海斯莱克实验动物有限责任公司,上海201615 [2]中国科学院上海生命科学研究院实验动物中心,上海201615 [3]南京农业大学动物医学院,南京210006
基金项目:上海市科委科研计划项目(11140902700),国家科技支撑计划课题(2013BAKIIB02).
摘    要:目的探讨EFS和DAP两种玻璃化冷冻方法对不同品系小鼠胚胎冷冻的效果。方法6个品系小鼠(KM、ICR、BALB/c、C57BL/6J、OB/OB、LAP/~TAOF59)的2-cell胚胎分别用EFS和DAP两种玻璃化冷冻方法进行冷冻和复苏,比较两种冷冻方法的胚胎复苏率和着床率。结果6个品系小鼠冷冻胚胎EFS方法的平均复苏率为69.97%(47.9%~83.6%),DAP方法的平均复苏率47.23%(26.3%-76.7%),EFS方法明显优于DAP方法。其中KM、ICR和BALB/c小鼠EFS方法的冷冻复苏率显著高于DAP方法(P〈0.01);冻融胚胎移植后EFS方法的平均着床率27.23%(1.75%一45.0%),DAP方法的平均着床率31.43%(7.0%一46.3%)。除KM、ICR小鼠外,其他4个品系小鼠的着床率DAP方法高于EFS方法。结论KM和ICR远交群小鼠胚胎适合用EFS方法冷冻保存;C57BL/6J、OB/OB、LAP/aTAOF59三个品系小鼠DAP方法优于EFS方法,但差异不大;BALB/c小鼠两种玻璃化冷冻方法的冻融胚胎着床率均较低,需进一步研究。

关 键 词:胚胎  玻璃化冷冻  复苏率  着床率  小鼠

Comparison of two vitrification-cryopreservation methods of embryos of various mouse strains
WANG Jun -fengI,LI Miao,ZHANG Yi-bao,YU Li-li,WEI Qin,LIU Li-junI,SHI Mei-lian,',XU Ping.Comparison of two vitrification-cryopreservation methods of embryos of various mouse strains[J].Chinese Journal of Laboratory Animal Science,2013(6):12-15.
Authors:WANG Jun -fengI  LI Miao  ZHANG Yi-bao  YU Li-li  WEI Qin  LIU Li-junI  SHI Mei-lian    XU Ping
Institution:1'2 (1. Shanghai SLAC Laboratory Animal Co. Ltd. , Shanghai 201615, China; 2. Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201615; 3. College of Veterinary Medicine, Nanjing Agriculture University, Nanjing 210006)
Abstract:Objective To compare the effect of two vitrification-cryopreservation methods of embryos of several mouse strains. Methods The two-cell embryos from six mouse strains (KM, ICR, BALB/c, C57BL/6J, OB/OB, LAP/ rtTAOF59) were cryopreserved and thawed, using EFS and DAP eryoprotectants, respectively. The recovery rate in vitro and implantation rate in vivo were determined to evaluate the efficacy of the two methods. Results The average post-thaw survival rates of the embryos of different strains preserved in EFS were 69.97% (47.9% to 83.6% ) , and preserved in DAP 47.23% (26. 3% to 76. 7% ). After 2-cell embryos were transferred to the oviducts of pseudopregnant recipient in all the strains, the implantation rates of EFS-vitrified embryos were ranged from 1.75% to 45.0% ( average 27.23% ) and ofDAP-vitrified embryos from 7.0% to 46. 3% (average 31.43% ). With the respect of recovery rate, EFS was preferred to DAP. No significant differences (P 〉 0. 05) were found between the implantation rates of EFS and DAP in KM and ICR strains. But the implantation rates of BALB/c, C57BL/6J, OB/OB, and LAP/rtTAOF59 mouse embryos in EFS were higher than those in DAP, respectively. Conclusions EFS cryoprotectant is suitable for both the KM and ICR mouse embryos vitrification-cryopreservation. DAP is somehow better than EFS for cryopreservation of C57BL/6J, OB/OB and LAP/rtTAOF59 mouse embryos, but with a non-significant difference between the two cryoprotectants. Both EFS and DAP show a rather low implantation rate of the BALB/c mouse embryos, therefore, further studies are needed to improve this issue.
Keywords:Embryo  Vitrification-eryopreservation  Recovery rate  Impantation rate  Mouse
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