Szczygiel Monika A, Kusakabe Hirokazu, Yanagimachi Ryuzo, Whittingham David G
Institute for Biogenesis Research, John A. Burns School of Medicine, University of Hawaii Medical School, 1960 East-West Road, Honolulu, HI 96822, USA.
Biol Reprod. 2002 Jul;67(1):287-92. doi: 10.1095/biolreprod67.1.287.
Success with in vitro fertilization (IVF) using inbred strains of mice varies considerably and appears to be related to the proportion of motile spermatozoa present in epididymal sperm samples of different strains. In this study, motile spermatozoa were separated from the original samples using a column of Sephadex G25. IVF rates were compared between separated and nonseparated samples of epididymal spermatozoa before and after cryopreservation. Oocytes and spermatozoa were obtained from FVB, DBA/2, C57BL/6J, and BALB/c inbred mice; and from F1 (C57BL/6J;ts DBA/2) hybrid mice, and isogenic gametes were used for IVF. These strains of mice were chosen because of their common use in transgenesis and mutagenesis studies. Dulbecco PBS was used for sperm separation on Sephadex, 18% raffinose, and 3% skim milk for cryopreservation; T6 medium for IVF; and mKSOM(AA) for embryo culture. There was a marked improvement in the rate of fertilization using fresh spermatozoa after motile spermatozoa were separated in C57BL/6J and BALB/c strains (92% vs. 58%, 79% vs. 44%) but no differences were found in fertilization rates between separated and nonseparated spermatozoa in F1, FVB, and DBA/2 strains (99% vs. 83%, 95% vs. 93%, 86% vs. 87%, respectively). After cryopreservation, higher rates of fertilization were obtained with separated motile samples in all strains; the greatest improvements were obtained with spermatozoa from C57BL/6J and BALB/c strains (40% vs. 16% and 51% vs. 14% for separated and nonseparated spermatozoa, respectively). No differences were found between the proportions of 14.5-day fetuses developing from embryos derived from separated and nonseparated spermatozoa with or without cryopreservation (33% to 46%). In conclusion, the fertility of frozen-thawed mouse epididymal spermatozoa improves significantly when highly motile populations of spermatozoa are separated for freezing.
使用近交系小鼠进行体外受精(IVF)的成功率差异很大,并且似乎与不同品系附睾精子样本中活动精子的比例有关。在本研究中,使用Sephadex G25柱从原始样本中分离出活动精子。比较了附睾精子冷冻保存前后分离样本和未分离样本的IVF率。卵母细胞和精子取自FVB、DBA/2、C57BL/6J和BALB/c近交系小鼠;以及F1(C57BL/6J;ts DBA/2)杂交小鼠,并使用同基因配子进行IVF。选择这些品系的小鼠是因为它们在转基因和诱变研究中常用。在Sephadex上使用杜尔贝科磷酸盐缓冲盐水(Dulbecco PBS)进行精子分离,使用18%棉子糖和3%脱脂牛奶进行冷冻保存;使用T6培养基进行IVF;使用mKSOM(AA)进行胚胎培养。在C57BL/6J和BALB/c品系中,分离出活动精子后,新鲜精子的受精率有显著提高(分别为92%对58%,79%对44%),但在F1、FVB和DBA/2品系中,分离和未分离精子的受精率没有差异(分别为99%对83%,95%对93%,86%对87%)。冷冻保存后,所有品系中分离的活动样本的受精率都更高;C57BL/6J和BALB/c品系的精子获得的改善最大(分离和未分离精子分别为40%对16%和51%对14%)。在有或没有冷冻保存的情况下,分离和未分离精子来源的胚胎发育成14.5天胎儿的比例没有差异(33%至46%)。总之,当分离出高活动力的精子群体进行冷冻时,冻融小鼠附睾精子的生育力显著提高。