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The improvement in fertilizing ability of cryopreserved mouse spermatozoa using laser-microdissected oocytes

  • Original Article
  • Embryo Manipulation
  • Published:
Reproductive Medicine and Biology

Abstract

Aim

The C57BL/6 mouse strain is now commonly used for producing transgenic/knockout strains. However, the fertilizing ability of these spermatozoa decreases as a result of cryopreservaion. Although the micromanipulation technique has been established to increase their fertilizing ability, it requires a considerable degree of technical skill. In the present report, we investigate the simple microdissection of zona pellucida by laser to increase the fertilizing ability of cryopreserved spermatozoa.

Methods

C57BL/6J spermatozoa were cryopreserved using a solution consisting of 18% raffinose/3% skim milk. Oocytes of the same strain were placed in PB1 medium containing 0, 0.25, 0.50 or 0.75 mol sucrose. The zona pellucida of oocytes was microdissected by laser with different pulse lengths selected from 0.45 to 0.65 ms. Microdissected oocytes were then fertilized with cryopreserved spermatozoa, and the subsequent development of embryos was assessed.

Results

When oocytes were microdissected in PB1 medium without sucrose, 81.5% of the oocytes were fertilized. The fertilization rates increased significantly as the pulse length was lengthened when compared with oocytes with intact zona pellucida. Furthermore, normal offspring were obtained in all experiments.

Conclusion

The fertilizing ability of cryopreserved spermatozoa is improved when oocytes with their zona pellucida microdissected by laser were used.

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References

  1. Okuyama M, Isogai S, Saga M, Hamada H, Ogawa S. In vitro fertilization (IVF) and artificial insemination (AI) by cryopreserved spermatozoa in mouse. J Fertil Implant 1990; 7: 116–119.

    Google Scholar 

  2. Tada N, Sato M, Yamanoi J, Mizorogi T, Kasai K, Ogawa S. Cryopreservation of mouse spermatozoa in the presence of raffinose and glycerol. J Reprod Fertil 1990; 89: 511–516.

    PubMed  CAS  Google Scholar 

  3. Yokoyama M, Akiba H, Katsuki M, Nomura T. Production of normal young following transfer of mouse embryos obtained by in vitro fertilization using cryopreserved spermatozoa. Exp Anim 1990; 39: 125–128.

    CAS  Google Scholar 

  4. Takeshima T, Nakagata N, Ogawa S. Cryopreservation of mouse spermatozoa. Exp Anim 1991; 40: 493–497.

    CAS  Google Scholar 

  5. Penfold LM, Moore HD. A new method for cryopreservation of mouse spermatozoa. J Reprod Fertil 1993; 99: 131–134.

    PubMed  CAS  Google Scholar 

  6. Songsasen N, Betteridge KJ, Leibo SP. Birth of live mice resulting from oocytes fertilized in vitro with cryopreserved spermatozoa. Biol Reprod 1997; 56: 143–152.

    Article  PubMed  CAS  Google Scholar 

  7. Nakagata N, Takeshima T. High fertilizing ability of mouse spermatozoa diluted slowly after cryopreservation. Theriogenology 1992; 37: 1283–1291.

    Article  Google Scholar 

  8. Nakagata N, Takeshima T. Cryopreservation of mouse spermatozoa from inbred and F1 hybrid strains. Exp Anim 1993; 42: 317–320.

    CAS  Google Scholar 

  9. Nakagata N, Ueda S, Yamanouchi K et al. Cryopreservation of wild mouse spermatozoa. Theriogenology 1995; 43: 635–643.

    Article  PubMed  CAS  Google Scholar 

  10. Nakagata N. Use of cryopreservation techniques of embryos and spermatozoa for production of transgenic (Tg) mice and for maintenance of Tg mouse lines. Laboratory Anim Sci 1996; 46: 236–238.

    CAS  Google Scholar 

  11. Knight J, Abbott A. Full house. Nature 2002; 417: 785–786.

    Article  PubMed  CAS  Google Scholar 

  12. Songsasen N, Leibo SP. Cryopreservation of mouse spermatozoa. II. Relationship between survival after cryopreservation and osmotic tolerance of spermatozoa from three strains of mice. Cryobiology 1997; 35: 255–269.

    Article  PubMed  CAS  Google Scholar 

  13. Thornton CE, Brown SD, Glenister PH. Large numbers of mice established by in vitro fertilization with cryopreserved spermatozoa: implications and applications for genetic resource banks, mutagenesis screens, and mouse backcrosses. Mamm Genome 1999; 10: 987–992.

    Article  PubMed  CAS  Google Scholar 

  14. Sztein IM, Farley JS, Mobraaten LE. In vitro fertilization with cryopreserved inbred mouse sperm. Biol Reprod 2000; 63: 1774–1780.

    Article  PubMed  CAS  Google Scholar 

  15. Nakagata N, Okamoto M, Ueda O, Suzuki H. Positive effect of partial zona-pellucida dissection on the in vitro fertilizing capacity of cryopreserved C57BL/6J transgenic mouse spermatozoa of low motility. Biol Reprod 1997; 57: 1050–1055.

    Article  PubMed  CAS  Google Scholar 

  16. Kawase Y, Iwata T, Ueda O et al. Effect of partial incision of the zona pellucida by piezo-micromanipulator for in vitro fertilization using frozen-thawed mouse spermatozoa on the developmental rate of embryos transferred at the 2-cell stage. Biol Reprod 2002; 66: 381–385.

    Article  PubMed  CAS  Google Scholar 

  17. Kawase Y, Aoki Y, Kamada N, Jishage K Suzuki H. Comparison of fertility between intracytoplasmic sperm injection and in vitro fertilization with a partial zona pellucida incision by using a piezo-micromanipulator in cryopreserved inbred mouse spermatozoa. Contemp Top Laboratory Anim Sci 2004; 43: 21–25.

    CAS  Google Scholar 

  18. Szczygiel MA, Kusakabe H, Yanagimachi R, Whittingham DG. Intracytoplasmic sperm injection is more efficient than in vitro fertilization for generating mouse embryos from cryopreserved spermatozoa. Biol Reprod 2002; 67: 1278–1284.

    Article  PubMed  CAS  Google Scholar 

  19. Sakamoto W, Kaneko T, Nakagata N. Use of frozen-thawed oocytes for efficient production of normal offspring from cryopreserved mouse spermatozoa showing low fertility. Comp Med 2005; 55: 136–139.

    PubMed  CAS  Google Scholar 

  20. Obruca A, Strohmer H, Sakkas D et al. Use of lasers in assisted fertilization and hatching. Hum Reprod 1994; 9: 1723–1726.

    PubMed  CAS  Google Scholar 

  21. Antinori S, Selman HA, Caffa B, Panci C, Dani GL, Versaci C. Zona opening of human embryos using a non-contact UV laser for assisted hatching in patients with poor prognosis of pregnancy. Hum Reprod 1996; 11: 2488–2492.

    PubMed  CAS  Google Scholar 

  22. Nakagata N. Cryopreservation of mouse spermatozoa. Mamm Genome 2000; 11: 572–576.

    Article  PubMed  CAS  Google Scholar 

  23. Quinn P, Kerin JF, Warnes GM. Improved pregnancy rate in human in vitro fertilization with the use of a medium based on the composition of human tubal fluid. Fertil Steril 1985; 44: 493–498.

    PubMed  CAS  Google Scholar 

  24. Whittingham DG. Embryo banks in the future of developmental genetics. Genetics 1974; 78: 395–402.

    PubMed  CAS  Google Scholar 

  25. Bath ML. Simple and efficient in vitro fertilization with cryopreserved C57BL/6J mouse sperm. Biol Reprod 2003; 68: 19–23.

    Article  PubMed  CAS  Google Scholar 

  26. Kaneko T, Whittingham DG, Yanagimachi R. Effect of pH value of freeze-drying solution on the chromosome integrity and developmental ability of mouse spermatozoa. Biol Reprod 2003; 68: 136–139.

    Article  PubMed  CAS  Google Scholar 

  27. Kaneko T, Whittingham DG, Overstreet JW, Yanagimachi R. Tolerance of the mouse sperm nuclei to freeze-drying depends on their disulfide status. Biol Reprod 2003; 69: 1859–1862.

    Article  PubMed  CAS  Google Scholar 

  28. Ward MA, Kaneko T, Kusakabe H, Biggers ID, Whittingham DG, Yanagimachi R. Long-term preservation of mouse spermatozoa after freeze-drying and freezing without cryoprotection. Biol Reprod 2003; 69: 2100–2108.

    Article  PubMed  CAS  Google Scholar 

  29. Kaneko T, Nakagata N. Relation between storage temperature and fertilizing ability of freeze-dried mouse spermatozoa. Comp Med 2005; 55: 140–144.

    PubMed  CAS  Google Scholar 

  30. Carthew P, Wood MJ, Kirby C. Pathogenicity of mouse hepatitis virus for preimplantation mouse embryos. J Reprod Fertil 1985; 73: 207–213.

    Article  PubMed  CAS  Google Scholar 

  31. Peters DD, Marschall S, Mahabir E et al. Risk assessment of mouse hepatitis virus infection via in vitro fertilization and embryo transfer by the use of zona-intact and lasermicrodissected oocytes. Biol Reprod 2006; 74: 246–252.

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Naomi Nakagata.

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Kaneko, T., Yanagi, M., Nakashima, T. et al. The improvement in fertilizing ability of cryopreserved mouse spermatozoa using laser-microdissected oocytes. Reprod Med Biol 5, 249–253 (2006). https://doi.org/10.1111/j.1447-0578.2006.00149.x

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  • DOI: https://doi.org/10.1111/j.1447-0578.2006.00149.x

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