Mouse Biology Program, School of Veterinary Medicine, University of California, Davis, California 95616, USA.
Reproduction. 2012 Apr;143(4):449-53. doi: 10.1530/REP-12-0005. Epub 2012 Jan 24.
Apolipoprotein E (Apoe)-deficient knockout mice were used to test the hypothesis that mutant mice preserved as evaporatively dried (ED) spermatozoa, stored at -80 °C for 6 months, and then recovered by ICSI will exhibit the same phenotype as before preservation. The birth rate of mice recovered by ICSI of evaporatively dried spermatozoa was lower than that of fresh spermatozoa (17.5 vs 38.0%). Progeny of mice preserved using evaporatively dried spermatozoa were reproductively sound. From these, the second generation of mice produced by natural mating showed lesions typical of APOE deficiency, including severe hypercholesterolemia, hypertriglyceridemia, markedly increased plasma low-density lipoprotein level, and extensive and severe atherosclerotic lesions in the aorta. We conclude that the expected phenotype caused by an induced genetic mutation can be faithfully recapitulated and sustained in subsequent generations of mice preserved and stored as ED spermatozoa and recovered using ICSI. Because it is simpler, faster, and cheaper than conventional (cryopreservation) and nonconventional (freeze-drying) preservation procedures, evaporative drying is a viable, cost-effective, and efficient method for preserving and storing valuable mutant mouse strains.
载脂蛋白 E (Apoe) 缺陷型敲除小鼠被用于测试以下假说,即经过蒸发干燥(ED)并在-80°C 下储存 6 个月的保存的突变型精子,通过 ICSI 恢复后,将表现出与保存前相同的表型。通过 ICSI 恢复的 ED 精子的受孕率低于新鲜精子(17.5% vs 38.0%)。使用 ED 精子保存的小鼠后代具有生殖能力。从这些精子中,通过自然交配产生的第二代小鼠表现出 APOE 缺陷的典型病变,包括严重的高胆固醇血症、高三酰甘油血症、显著增加的血浆低密度脂蛋白水平,以及主动脉广泛而严重的动脉粥样硬化病变。我们得出结论,通过诱导基因突变产生的预期表型可以在随后的几代通过 ICSI 恢复的 ED 精子保存和储存的小鼠中被忠实地再现和维持。因为与传统(冷冻保存)和非传统(冻干)保存方法相比,蒸发干燥更简单、更快且更便宜,所以蒸发干燥是一种可行、具有成本效益且高效的保存和储存有价值的突变型小鼠品系的方法。