Recent improvements in sperm cryopreservation and IVF protocols in mice established sperm cryopreservation as a reliable and efficient method for archiving and distributing genetically engineered mouse lines. Further, the ability to rapidly expand animal model colonies from frozen sperm make sperm cryopreservation a quick and effective method for the distribution and restoration of mouse lines.
- Sperm cryopreservation is the most common method for cryopreserving mouse lines.
- Sperm cryopreservation is simple, fast, and requires just two breeding-age males.
- It is the most economical option for mouse lines carrying single genetic mutations/modification on a standard inbred strain genetic background.
- 100% of pups born using frozen sperm harvested from homozygous males, and 50% of pups born using sperm harvested from heterozygous/hemizygous males, carry the genetic modification.
This is the third of a four-part series on the effective use of cryopreservation in maintaining genetically modified mouse and rat lines:
- Cryopreservation in Colony Management
- Introduction to Embryo Cryopreservation
- Sperm Cryopreservation Overview
- Cryopreservation Decision Tree
Introduction to Sperm Cryopreservation
For several years, embryo cryopreservation was the only practical option for securing lines of laboratory rodents. The advent of sperm cryopreservation as a popular alternative in 19921 now provides investigators with two options.Because cryopreservation of sperm has several advantages over working with embryos, and it became the dominant preservation format over the past ten years. Successful sperm cryopreservation can be achieved using one-to-two adult male mice preferably known to be fertile, commercially available reagents, and a basic understanding of the mouse male reproductive anatomy. With these in hand, and perhaps some trial runs, one could easily collect and cryopreserve sperm from a mouse model with confidence for recovery in the future.
Sperm Cryopreservation Basics
Reproducible techniques for the cryopreservation of spermatozoa from laboratory mice were not available until twenty years1 after the first successful embryo cryopreservation. The breakthrough method described cooling sperm in a solution of 18% raffinose and 3% skim milk powder in the vapor phase of liquid nitrogen for 10 minutes, then plunging the material into liquid nitrogen for cryostorage.Widespread adoption of this method was initially limited by the inefficient recovery of the sperm from many important inbred strains, including the widely used C57BL/6.
While the fertility of frozen-thawed sperm was found to be comparable to that of freshly harvested sperm in some hybrid and outbred strains of mice, the fertility of frozen-thawed C57BL/6 (and other inbred strains) sperm was found to be unpredictable.
Further advances in sperm cryopreservation over the last decade2,3,4 overcame these challenges and support reliable cryopreservation of sperm from multiple inbred and outbred strains of laboratory mice. These advances include the addition of reducing agents to the standard cryoprotectant medium: monothioglycerol to prevent the overproduction of reactive oxygen species2 and glutamine to protect sperm from membrane damage4.
The effectiveness of these improvements in sperm cryopreservation was further amplified by advances in IVF5 that significantly improved the fertilization rates for frozen-thawed sperm.
Advantages
- Simple, fast procedure that does not need expensive equipment.
- Requires two breeding age males for cryopreservation of 15-20 straws of sperm.
- Low upfront cost.
- Ability to generate hundreds of pups from one straw of sperm.
Limitations
- Recovery requires the use of oocyte donors and in vitro fertilization technology.
- Sperm are haploid cells, requiring the complementation of the other half of the genome from oocytes, therefore cannot be used to preserve mouse models on mixed or complex genetic backgrounds.
- Lines that carry multiple mutations/modifications may require downstream breeding to recapitulate the genetic constitution of the original breeding colony.
- Sperm viability is strain— and sometimes individual male-dependent.
- Currently not available in rats.
Sperm Cryopreservation vs Embryo Cryopreservation
The most fundamental difference between cryopreserving sperm and embryos is the sperm are gametes, and therefore haploid. Only half of the genetic material from the modified line is being preserved.Upon recovery and return to the diploid state through fertilization of an oocyte and generation of a zygote, the complementary haploid genome from the oocyte is at best the same background genetic strain. To account for this, sperm cryopreservation is typically used when preserving a genetically modified line on a congenic, inbred background strain.
Recovering the line using oocyte donors from the same inbred background strain could be considered a "genetic refresh", but technically is not a change in genetic background. Cryopreserved sperm with oocytes from a desired background can be used to transfer a genetically engineered model onto a new genetics background, however, as the first generation backcross.
A second important consideration with sperm cryopreservation is that all offspring resulting from cryopreservation are heterozygous for the desired genetic modification (assuming the cryopreserved sperm were harvested from a male that was homozygous). If study animals must be homozygous, then one additional round of natural breeding using heterozygous, cryopreserved males and females is required to generate a cohort of homozygous animals for study. In contrast, if one cryopreserves homozygous embryos, the offspring upon recovery can be moved directly into study.
The above limitation are of greater concern if the line is carrying multiple genetic modifications. Having multiple genetic modifications recovered, each in the heterozygous state, could require several rounds of downstream breeding to return all genetic modifications to homozygosity. Embryo cryopreservation is the preferred method for lines carrying multiple genetic modifications.
Common Questions about Sperm Cryopreservation
Q: How important is quality control when cryopreserving sperm?
Sperm quality can be influenced by the genetic background, technical skill, the quality of cryoprotective media used, and occasionally by the male sperm donor itself. If the cryopreserved material is intended to serve as the sole source of material to recover a genetically modified line for later use, one must have the highest degree of confidence in the cryopreserved material.
Post-cryo quality assessment should minimally include measuring the fertilization rate of the cryopreserved sperm in an in vitro fertilization assay, as determined by the percent of oocytes that are fertilized and develop to the two-cell stage within twenty-four hours. In general, a post-cryo fertilization rate of 15% is sufficient to give a high degree of confidence the line is recoverable from the remaining cryopreserved material (provided there is no failure in storage).
If one wishes to add an additional level of confidence, the quality assurance program can be extended to transfer of the resulting embryos to a recipient female and allowing the pregnancy to go to term to generate live born offspring.
How many straws of sperm are required for effective preservation?
This volume of material is generally aliquoted across 10-20 individual straws, making dividing the material for "dual-site storage" quite easy.
What is the longevity of frozen sperm?
Unlike frozen embryos, frozen sperm is less sensitive to temperature fluctuations and even temporary storage of frozen mouse sperm on dry ice for 3 to 4 days is reported to have not compromise fertility7.
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