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Closed vitrification of mouse oocytes using the CryoLogic vitrification method: A modification that improves developmental competence

  • Jo, Jun Woo (Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seoul National University College of Medicine) ;
  • Jee, Byung Chul (Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seoul National University College of Medicine) ;
  • Suh, Chang Suk (Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seoul National University College of Medicine) ;
  • Kim, Seok Hyun (Department of Obstetrics and Gynecology, Seoul National University College of Medicine)
  • Received : 2013.10.25
  • Accepted : 2013.12.23
  • Published : 2013.12.31

Abstract

Objective: To compare the mouse oocyte vitrification outcomes of the CryoLogic vitrification method (CVM) and the conventional open method using a Cryotop. Two CVM methods (original CVM and modified CVM) were tested. Methods: Mature oocytes obtained from female BDF-1 mice were vitrified by two-step exposure to equilibrium and vitrification solutions. Three vitrification protocols were tested on three groups: the CVM-kit, modified CVM, and Cryotop groups. After exposure to the two solutions, the oocytes were vitrified. After warming, the oocytes were fertilized in vitro, and the embryo development was assessed. Blastomeres positive for caspase were counted using an in situ assay kit. The spindle morphology and chromosome configurations of warmed vitrified oocytes were also assessed. Results: The modified CVM and Cryotop groups showed similar developmental capacities, and similar proportions of cells with intact spindles and chromosome configurations. The modified CVM protocol was superior to the original CVM protocol for developmental competence and intact spindle preservation. However, the CVM group showed a relatively higher number of apoptotic cells in blastocysts. Conclusion: Closed vitrification using the modified CVM protocol may be used as an alternative to the conventional open method, but strategies to decrease apoptosis in the blastomere need to be investigated.

Keywords

References

  1. Ubaldi F, Anniballo R, Romano S, Baroni E, Albricci L, Colamaria S, et al. Cumulative ongoing pregnancy rate achieved with oocyte vitrification and cleavage stage transfer without embryo selection in a standard infertility program. Hum Reprod 2010;25:1199-205. https://doi.org/10.1093/humrep/deq046
  2. Cobo A, Meseguer M, Remohi J, Pellicer A. Use of cryo-banked oocytes in an ovum donation programme: a prospective, randomized, controlled, clinical trial. Hum Reprod 2010;25:2239-46. https://doi.org/10.1093/humrep/deq146
  3. Cobo A, Romero JL, Perez S, de los Santos MJ, Meseguer M, Remohi J. Storage of human oocytes in the vapor phase of nitrogen. Fertil Steril 2010;94:1903-7. https://doi.org/10.1016/j.fertnstert.2009.10.042
  4. Nagy ZP, Chang CC, Shapiro DB, Bernal DP, Kort HI, Vajta G. The efficacy and safety of human oocyte vitrification. Semin Reprod Med 2009;27:450-5. https://doi.org/10.1055/s-0029-1241054
  5. Smith GD, Serafini PC, Fioravanti J, Yadid I, Coslovsky M, Hassun P, et al. Prospective randomized comparison of human oocyte cryopreservation with slow-rate freezing or vitrification. Fertil Steril 2010;94:2088-95. https://doi.org/10.1016/j.fertnstert.2009.12.065
  6. Bielanski A, Bergeron H, Lau PC, Devenish J. Microbial contamination of embryos and semen during long term banking in liquid nitrogen. Cryobiology 2003;46:146-52. https://doi.org/10.1016/S0011-2240(03)00020-8
  7. Bielanski A, Nadin-Davis S, Sapp T, Lutze-Wallace C. Viral contamination of embryos cryopreserved in liquid nitrogen. Cryobiology 2000;40:110-6. https://doi.org/10.1006/cryo.1999.2227
  8. Parmegiani L, Cognigni GE, Filicori M. Ultra-violet sterilization of liquid nitrogen prior to vitrification. Hum Reprod 2009;24:2969. https://doi.org/10.1093/humrep/dep329
  9. Parmegiani L, Accorsi A, Cognigni GE, Bernardi S, Troilo E, Filicori M. Sterilization of liquid nitrogen with ultraviolet irradiation for safe vitrification of human oocytes or embryos. Fertil Steril 2010; 94:1525-8. https://doi.org/10.1016/j.fertnstert.2009.05.089
  10. Sripunya N, Somfai T, Inaba Y, Nagai T, Imai K, Parnpai R. A comparison of cryotop and solid surface vitrification methods for the cryopreservation of in vitro matured bovine oocytes. J Reprod Dev 2010;56:176-81. https://doi.org/10.1262/jrd.09-108H
  11. Beebe LF, Bouwman EG, McIlfatrick SM, Nottle MB. Piglets produced from in vivo blastocysts vitrified using the Cryologic Vitrification Method (solid surface vitrification) and a sealed storage container. Theriogenology 2011;75:1453-8. https://doi.org/10.1016/j.theriogenology.2010.11.043
  12. Sanchez-Partida LG, Kelly RD, Sumer H, Lo CY, Aharon R, Holland MK, et al. The generation of live offspring from vitrified oocytes. PLoS One 2011;6:e21597. https://doi.org/10.1371/journal.pone.0021597
  13. Wang X, Catt S, Pangestu M, Temple-Smith P. Live offspring from vitrified blastocysts derived from fresh and cryopreserved ovarian tissue grafts of adult mice. Reproduction 2009;138:527-35. https://doi.org/10.1530/REP-09-0148
  14. Wang X, Catt S, Pangestu M, Temple-Smith P. Successful in vitro culture of pre-antral follicles derived from vitrified murine ovarian tissue: oocyte maturation, fertilization, and live births. Reproduction 2011;141:183-91. https://doi.org/10.1530/REP-10-0383
  15. Huang JY, Buckett WM, Gilbert L, Tan SL, Chian RC. Retrieval of immature oocytes followed by in vitro maturation and vitrification: a case report on a new strategy of fertility preservation in women with borderline ovarian malignancy. Gynecol Oncol 2007; 105:542-4. https://doi.org/10.1016/j.ygyno.2007.01.036
  16. Chian RC, Huang JY, Tan SL, Lucena E, Saa A, Rojas A, et al. Obstetric and perinatal outcome in 200 infants conceived from vitrified oocytes. Reprod Biomed Online 2008;16:608-10. https://doi.org/10.1016/S1472-6483(10)60471-3
  17. Yoon TK, Kim TJ, Park SE, Hong SW, Ko JJ, Chung HM, et al. Live births after vitrification of oocytes in a stimulated in vitro fertilization- embryo transfer program. Fertil Steril 2003;79:1323-6. https://doi.org/10.1016/S0015-0282(03)00258-9
  18. Lucena E, Bernal DP, Lucena C, Rojas A, Moran A, Lucena A. Successful ongoing pregnancies after vitrification of oocytes. Fertil Steril 2006;85:108-11. https://doi.org/10.1016/j.fertnstert.2005.09.013
  19. Rienzi L, Romano S, Albricci L, Maggiulli R, Capalbo A, Baroni E, et al. Embryo development of fresh 'versus' vitrified metaphase II oocytes after ICSI: a prospective randomized sibling-oocyte study. Hum Reprod 2010;25:66-73. https://doi.org/10.1093/humrep/dep346
  20. Katayama KP, Stehlik J, Kuwayama M, Kato O, Stehlik E. High survival rate of vitrified human oocytes results in clinical pregnancy. Fertil Steril 2003;80:223-4.
  21. Nagy ZP, Chang CC, Shapiro DB, Bernal DP, Elsner CW, Mitchell- Leef D, et al. Clinical evaluation of the efficiency of an oocyte donation program using egg cryo-banking. Fertil Steril 2009;92: 520-6. https://doi.org/10.1016/j.fertnstert.2008.06.005
  22. Bielanski A, Vajta G. Risk of contamination of germplasm during cryopreservation and cryobanking in IVF units. Hum Reprod 2009;24:2457-67. https://doi.org/10.1093/humrep/dep117
  23. Parmegiani L, Cognigni GE, Bernardi S, Cuomo S, Ciampaglia W, Infante FE, et al. Efficiency of aseptic open vitrification and hermetical cryostorage of human oocytes. Reprod Biomed Online 2011;23:505-12. https://doi.org/10.1016/j.rbmo.2011.07.003
  24. Kuleshova LL, Shaw JM. A strategy for rapid cooling of mouse embryos within a double straw to eliminate the risk of contamination during storage in liquid nitrogen. Hum Reprod 2000;15: 2604-9. https://doi.org/10.1093/humrep/15.12.2604
  25. Isachenko V, Montag M, Isachenko E, Zaeva V, Krivokharchenko I, Shafei R, et al. Aseptic technology of vitrification of human pronuclear oocytes using open-pulled straws. Hum Reprod 2005; 20:492-6. https://doi.org/10.1093/humrep/deh605
  26. Cremades N, Sousa M, Silva J, Viana P, Sousa S, Oliveira C, et al. Experimental vitrification of human compacted morulae and early blastocysts using fine diameter plastic micropipettes. Hum Reprod 2004;19:300-5. https://doi.org/10.1093/humrep/deh059
  27. Kuwayama M, Vajta G, Ieda S, Kato O. Comparison of open and closed methods for vitrification of human embryos and the elimination of potential contamination. Reprod Biomed Online 2005; 11:608-14. https://doi.org/10.1016/S1472-6483(10)61169-8
  28. Vanderzwalmen P, Zech N, Prapas Y, Panagiotidis Y, Papatheodorou A, Lejeune B, et al. Closed carrier device: a reality to vitrify oocytes and embryos in aseptic conditions. Gynecol Obstet Fertil 2010;38:541-6. https://doi.org/10.1016/j.gyobfe.2010.07.011
  29. Mazur P, Seki S. Survival of mouse oocytes after being cooled in a vitrification solution to -196 degrees C at 95 degrees to 70,000 degrees C/min and warmed at 610 degrees to 118,000 degrees C/min: a new paradigm for cryopreservation by vitrification. Cryobiology 2011;62:1-7. https://doi.org/10.1016/j.cryobiol.2010.10.159

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