Raspa Marcello, Fray Martin, Paoletti Renata, Montoliu Lluis, Giuliani Alessandro, Scavizzi Ferdinando
National Research Council (IBCN), CNR-Campus International Development (EMMA-INFRAFRONTIER-IMPC), Monterotondo Scalo, Rome, Italy.
Mary Lyon Centre, MRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, United Kingdom.
Theriogenology. 2018 Oct 1;119:52-59. doi: 10.1016/j.theriogenology.2018.06.020. Epub 2018 Jun 28.
The mouse is widely used for biomedical research and an increasing number of genetically altered models are currently generated, therefore centralized repositories are essentials to secure the important mouse strains that have been developed. We have previously reported that spermatozoa of wild type and mutant strains frozen using standard laboratory protocols can be transported in dry ice (-79 °C) for 7 days and safely stored in a -80 °C freezer for up to two years. The objective of this new study was to compare the effects of the freezing techniques using LN or -80 °C freezer on fertility of frozen-thawed mouse spermatozoa. After thawing, sperm fertility was comparable (P > 0,05) between the LN and the -80 °C samples for at least 1 year. Furthermore, we showed that it is possible to freeze and store mouse semen directly at -80 °C and eventually transfer it to LN irrespective of storage time. This study is relevant because it shows for the first time that mouse spermatozoa can be efficiently frozen and stored at -80 °C with no use of liquid nitrogen for a long period of time. A new, simple, efficient and flexible, liquid nitrogen free, method was developed for freezing and maintaining spermatozoa of wild type and mutant C57BL/6N lines. Lines on this genetic background are used in collaborative research infrastructures for systematic phenotyping, e.g. the International Mouse Phenotyping Consortium (IMPC) and therefore largely cryopreserved in repositories like EMMA/Infrafrontier. The importance of this finding will be especially useful for small laboratories with no or limited access to liquid nitrogen and for laboratories generating many mouse mutant lines by CRISPR/Cas9 who do not want to saturate the limited space of a LN tank, using a more accessible -80 °C freezer. This study underlines, once more, that mouse spermatozoa are very resistant and can be frozen, transported, shared and stored at -80 °C for a long time without a significant loss of viability. This new approach simplifies the freezing process and facilitates the long term storage of mouse spermatozoa at -80 °C, always allowing the transfer to LN for indefinite storage without noticeable detrimental effects.
小鼠被广泛用于生物医学研究,目前产生的基因改造模型数量不断增加,因此集中式储存库对于保存已培育出的重要小鼠品系至关重要。我们之前曾报道,使用标准实验室方案冷冻的野生型和突变株精子可在干冰(-79°C)中运输7天,并可在-80°C冰箱中安全储存长达两年。这项新研究的目的是比较使用液氮或-80°C冰箱的冷冻技术对冻融小鼠精子生育力的影响。解冻后,液氮和-80°C样本之间的精子生育力至少在1年内相当(P>0.05)。此外,我们表明,无论储存时间如何,都可以直接在-80°C冷冻并储存小鼠精液,最终将其转移到液氮中。这项研究具有重要意义,因为它首次表明,小鼠精子可以在不使用液氮的情况下在-80°C高效冷冻并长期储存。开发了一种新的、简单、高效且灵活的无液氮方法,用于冷冻和保存野生型和突变C57BL/6N品系的精子。具有这种遗传背景的品系用于协作研究基础设施进行系统表型分析,例如国际小鼠表型分析联盟(IMPC),因此在EMMA/Infrafrontier等储存库中大量冷冻保存。这一发现的重要性对于无法获得或只能有限获得液氮的小型实验室,以及通过CRISPR/Cas9产生许多小鼠突变株且不想占用液氮罐有限空间的实验室(使用更易于使用的-80°C冰箱)将特别有用。这项研究再次强调,小鼠精子具有很强的耐受性,可以在-80°C冷冻、运输、共享和储存很长时间而不会显著丧失活力。这种新方法简化了冷冻过程,并便于在-80°C长期储存小鼠精子,始终允许转移到液氮中进行无限期储存而不会产生明显的有害影响。