Small-volume vitrification and rapid warming yield high survivals of one-cell rat embryos in cryotubes†.

Abstract

To cryopreserve cells, it is essential to avoid intracellular ice formation during cooling and warming. One way to achieve this is to convert the water inside the cells into a non-crystalline glass. It is currently believed that to accomplish this vitrification, the cells must be suspended in a very high concentration (20-40%) of a glass-inducing solute, and subsequently cooled very rapidly. Herein, we report that this belief is erroneous with respect to the vitrification of one-cell rat embryos. In the present study, one-cell rat embryos were vitrified with 5μL of EFS10 (a mixture of 10% ethylene glycol (EG), 27% Ficoll, and 0.45M sucrose) in cryotubes at a moderate cooling rate, and warmed at various rates. Survival was assessed according to the ability of the cells to develop into blastocysts and to develop to term. When embryos were vitrified at a 2613°C/min cooling rate and thawed by adding 1mL of sucrose solution (0.3M, 50°C) at a warming rate of 18 467°C/min, 58.1±3.5% of the EFS10-vitrified embryos developed into blastocysts, and 50.0±4.7% developed to term. These rates were similar to those of non-treated intact embryos. Using a conventional cryotube, we achieved developmental capabilities in one-cell rat embryos by rapid warming that were comparable to those of intact embryos, even using low concentrations (10%) of cell-permeating cryoprotectant and at low cooling rates.