Abstract

BackgroundSimple and effective cryopreservation of human oocytes would have an enormous impact on the financial and ethical constraints of human assisted reproduction. Recently, studies have demonstrated the potential for cryopreservation in an ice-free glassy state by equilibrating oocytes with high concentrations of cryoprotectants (CPAs) and rapidly cooling to liquid nitrogen temperatures. A major difficulty with this approach is that the high concentrations required for the avoidance of crystal formation (vitrification) also increase the risk of osmotic and toxic damage. We recently described a mathematical optimization approach for designing CPA equilibration procedures that avoid osmotic damage and minimize toxicity, and we presented optimized procedures for human oocytes involving continuous changes in solution composition.MethodsHere we adapt and refine our previous algorithm to predict piecewise-constant changes in extracellular solution concentrations in order to make the predicted procedures easier to implement. Importantly, we investigate the effects of using alternate equilibration endpoints on predicted protocol toxicity. Finally, we compare the resulting procedures to previously described experimental methods, as well as mathematically optimized procedures involving continuous changes in solution composition.ResultsFor equilibration with CPA, our algorithm predicts an optimal first step consisting of exposure to a solution containing only water and CPA. This is predicted to cause the cells to initially shrink and then swell to the maximum cell volume limit. To reach the target intracellular CPA concentration, the cells are then induced to shrink to the minimum cell volume limit by exposure to a high CPA concentration. For post-thaw equilibration to remove CPA, the optimal procedures involve exposure to CPA-free solutions that are predicted to cause swelling to the maximum volume limit. The toxicity associated with these procedures is predicted to be much less than that of conventional procedures and comparable to that of the corresponding procedures with continuous changes in solution composition.ConclusionsThe piecewise-constant procedures described in this study are experimentally facile and are predicted to be less toxic than conventional procedures for human oocyte cryopreservation. Moreover, the mathematical optimization approach described here will facilitate the design of cryopreservation procedures for other cell types.

Highlights

  • Cryopreservation theoretically allows nearly indefinite storage of viable biological material [1]

  • Once the upper volume limit was reached, the ethylene glycol (EG) concentration was increased and maintained near osmotic equilibrium at a concentration that resulted in a volumetric influx of EG that was exactly balanced by efflux of water

  • When the goal state consisted of an intracellular EG concentration of 6 mol/L and a final cell volume that was equal to the isotonic volume, cell shrinkage at the end of EG loading terminated at the isotonic cell volume, as expected

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Summary

Introduction

Cryopreservation theoretically allows nearly indefinite storage of viable biological material [1]. Conventional cryopreservation techniques are usually thought of as slowcooling methods (~1°C/min) that utilize relatively low (1 to 2 mol/L) concentrations of cryoprotectants (CPAs) such as glycerol, ethylene glycol, or dimethyl sulfoxide. These conventional techniques are sufficient for many cell types, this approach is less successful for cells that have a reduced tolerance to sub-physiologic temperatures (e.g. oocytes [2,3]) or are damaged by extracellular ice formation (e.g., three dimensional tissues [4,5]). We recently described a mathematical optimization approach for designing CPA equilibration procedures that avoid osmotic damage and minimize toxicity, and we presented optimized procedures for human oocytes involving continuous changes in solution composition

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