Cold Storage and Cryopreservation Methods for Spermatozoa of the Sea Urchin, Lytechinus pictus .
Vacquier, V.; Hamdoun, A.
Show abstract
Sea urchins have contributed greatly to knowledge of fertilization, embryogenesis and cell biology. However, until now, they have not been a genetic model organism because of the long generation times of commonly used species, and lack of tools for husbandry and genetic manipulation. We recently established Lytechinus pictus, as a multigenerational sea urchin model, because of its relatively short generation time of 4-6 months and ease of laboratory culture. To take full advantage of this new multigenerational species, methods are needed to biobank and share mutant L. pictus sperm. Here, we describe a new extender based on sperm ion physiology before spawning of sperm into seawater. This extender maintains sperm capable of fertilization for at least 5-10 weeks when stored at 0 {degrees}C. We use the extender, and the cryoprotectant dimethyl sulfoxide (DMSO), to cryopreserve sperm of both L. pictus, and the widely used sea urchin, Strongylocentrotus purpuratus. The simple methods we describe work well for both species, achieving > 90% development and producing larvae that successfully undergo metamorphosis to juvenile sea urchins. Sperm of these two species can be frozen and thawed at least twice and still give rise to larvae that undergo metamorphosis. Main PointsO_LISperm can maintain fertilizing capacity ex vivo for 5-10 weeks when stored at 0{degrees}C. C_LIO_LIWhen freezing in liquid nitrogen no stepwise addition of cryoprotectant, or stepwise drop in temperature are required. C_LIO_LIA standard fertilization assay is presented to score cleavage stage sea urchin embryos produced by cryopreserved sperm. C_LIO_LISperm frozen and thawed more than once can produce larvae. C_LI
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