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Effects of different extenders on DNA integrity of boar spermatozoa following freezing-thawing.不同稀释液对猪精子冻融后DNA完整性的影响。
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Clin Biochem Rev. 2004 Feb;25(1):81-93.
5
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Comp Med. 2007 Oct;57(5):469-75.
6
Long-term storage of mouse spermatozoa after evaporative drying.蒸发干燥后小鼠精子的长期储存。
Reproduction. 2007 May;133(5):919-29. doi: 10.1530/REP-06-0096.
7
Damage to chromosomes and DNA of rhesus monkey sperm following cryopreservation.冷冻保存后恒河猴精子染色体和DNA的损伤
J Androl. 2007 Jul-Aug;28(4):493-501. doi: 10.2164/jandrol.106.000869. Epub 2007 Jan 24.
8
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Cell. 2007 Jan 12;128(1):9-13. doi: 10.1016/j.cell.2006.12.018.
9
Mouse sperm desiccated and stored in trehalose medium without freezing.小鼠精子在海藻糖培养基中干燥保存而不冷冻。
Biol Reprod. 2005 Oct;73(4):627-33. doi: 10.1095/biolreprod.105.042291. Epub 2005 Jun 1.
10
Detection of DNA damage in response to cooling injury in equine spermatozoa using single-cell gel electrophoresis.
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通过 ICSI 对干燥精子进行注射得到的突变小鼠表现出预期的表型。

Mutant mice derived by ICSI of evaporatively dried spermatozoa exhibit expected phenotype.

机构信息

Mouse Biology Program, School of Veterinary Medicine, University of California, Davis, California 95616, USA.

出版信息

Reproduction. 2012 Apr;143(4):449-53. doi: 10.1530/REP-12-0005. Epub 2012 Jan 24.

DOI:10.1530/REP-12-0005
PMID:22274886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3738174/
Abstract

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.

摘要

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。