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Long-term cryopreservation of mouse sperm

机译:小鼠精子的长期冷冻保存

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The objective was to determine if mouse sperm can maintain their fertilizing ability after being frozen for 10 y and whether the offspring derived from these sperm had normal fertilizing ability and phenotype. We cryopreserved sperm from six strains of mice (C57BL/6J, DBA/2N, BALB/cA, C3H/HeJ, B6D2F1 and B6C3F1) in a solution containing 18% (w/v) raffinose and 3% (w/v) skim milk, and preserved them in liquid nitrogen for 10 y. To assess the normality and fertilizing ability of these sperms, they were thawed and used for in vitro fertilization of oocytes of the same strains. Fertilization rates for C57BL/6J, DBA/2N, BALB/cA, C3H/HeJ, B6D2F1 and B6C3F1 were 66.4, 92.3, 72.8, 32.9, 60.3 and 53.7%, respectively. Furthermore, 38.3, 15.0, 43.3, 26.1, 38.3 and 16.7% of the embryos transferred to pseudopregnant females developed and produced live offspring that had normal phenotype and fertility.
机译:目的是确定小鼠精子在冷冻超过10年后是否能够维持其受精能力,以及衍生自这些精子的后代是否具有正常的受精能力和表型。我们在含有18%(w / v)棉子糖和3%(w / v)脱脂液的溶液中冷冻保存了六种小鼠小鼠的精子(C57BL / 6J,DBA / 2N,BALB / cA,C3H / HeJ,B6D2F1和B6C3F1)牛奶,并在液氮中保存> 10年。为了评估这些精子的正常性和受精能力,将它们融化并用于相同菌株的卵母细胞的体外受精。 C57BL / 6J,DBA / 2N,BALB / cA,C3H / HeJ,B6D2F1和B6C3F1的受精率分别为66.4、92.3、72.8、32.9、60.3和53.7%。此外,转移到假孕雌性中的胚胎的38.3%,15.0%,43.3%,26.1%,38.3%和16.7%发育并产生了具有正常表型和受精能力的活后代。

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