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Moderate heat treatment increases the penetrability of zonae pellucidae of salt-stored mammalian oocytes by spermatozoa

Published online by Cambridge University Press:  26 September 2008

Ryuzo Yanagimachi*
Affiliation:
Department of Anatomy and Reproductive Biology, University of Hawaii, Hawaii
Haruo Katayose
Affiliation:
Department of Anatomy and Reproductive Biology, University of Hawaii, Hawaii
Gary Killian
Affiliation:
Department of Anatomy and Reproductive Biology, University of Hawaii, Hawaii
Chin N. Lee
Affiliation:
Department of Anatomy and Reproductive Biology, University of Hawaii, Hawaii
Douglas T. Carrell
Affiliation:
Department of Anatomy and Reproductive Biology, University of Hawaii, Hawaii
Thomas T.F. Huang
Affiliation:
Department of Anatomy and Reproductive Biology, University of Hawaii, Hawaii
*
R. Yanagimachi, Department of Anatomy and Reproductive Biology, University of Hawaii School of Medicine, Honolulu, Hawaii 96822, USA. Tel: (808) 956-8746. Fax: (808) 956-5474.

Summary

The zona pellucida of mammalian oocytes stored in highly concentrated solutions of neutral salts is known to retain its biological and biochemical properties. However, the zona may become resistant to sperm penetration as the storage period is increased. In cattle and hamsters, the penetrability of zonae of salt-stored oocytes was restored or increased by treating the oocytes with moderate heat without altering the gross morphology of the zona. Although this technique did not work for salt-stored human ova, this may have been due to the use of so-called inseminated- unfertilised ova which (1) may have been fertilised but failed to activate, or (2) were not fertilised because of functionally defective zonae.

Type
Article
Copyright
Copyright © Cambridge University Press 1993

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References

Andrews, J.C., Howard, J.G., et al. (1992). Sperm capacitation in the domestic cat (Felis catus) and leopard cat (Felis bengalensis) as studied with a salt-stored zona pellucida penetration assay. Mol. Reprod. Dev. 31, 200–7.CrossRefGoogle ScholarPubMed
Bedford, J.M. & Kim, H.H. (1993). Sperm/egg binding patterns and oocyte cytology in retrospective analysis of fertilization failure in vitro. Human Reparod. 8, 453–63.CrossRefGoogle ScholarPubMed
Berkeley, A.S., Bedford, J.M. & Rosenwaks, Z. (1991). Clinical aspects of human in vitro fertilization. In: Elements of Mammalian Fertilization, ed. Wassarman, P., Vol. 2, pp. 3361. Boca Raton: CRC Press.Google Scholar
Biery, K.A., Maclean, R.A., et al. (1992). Penetration of capacitated sperm into the perivitelline space of salt-stored follicular oocytes in the bovine. Theriogenology 37, 193.CrossRefGoogle Scholar
Biggers, J.D., Whitten, W.K. & Whittingham, D.G. (1971). The culture of mouse embryos in vitro. In: Methods in Mammalian Embryology, ed. Daniel, J.C., pp. 86116. San Francisco: W.H. Freeman.Google Scholar
Boatman, D.E., Andrews, J.C. & Bavister, B.D. (1988). Quantitative assay for capacitation: evaluation of multiple sperm penetration through the zona pellucida of salt-stored hamster eggs. Gamete Res. 19, 1929.CrossRefGoogle ScholarPubMed
Chian, R.C., Niwa, K. & Okuda, K. (1991). In vitro penetration of zona pellucida of salt-stored bovine oocytes before and after maturation by frozen-thawed spermatozoa. Theriogenology 36, 209–19.CrossRefGoogle ScholarPubMed
Cummins, J.M. & Yanagimachi, R. (1986). Development of ability to penetrate the cumulus oophorus by hamster spermatozoa capacitated in vitro, in relation to the timing of the acrosome reaction. Gamete Res. 15, 187212.CrossRefGoogle Scholar
Donoghue, A.M., Howard, J.G., Byers, A.P., et al. (1992). Correlation of sperm viability with gamete interaction and fertilization in vitro in the cheetah (Acinonyx jibatus). Biol. Reprod. 46, 1047–56.CrossRefGoogle Scholar
Fayrer-Hosken, R.A. & Brackett, B.G. (1987). Use of saltstored zonae pellucidae for assessing rabbit sperm capacitation for in vitro fertilization. Gamete Res. 17, 191201.CrossRefGoogle ScholarPubMed
Fleming, A.D. & Yanagimachi, R. (1980). Superovulation and superpregnancy in the golden hamster. Dev. Growth Differ. 22, 103–12.CrossRefGoogle ScholarPubMed
Franken, D.R., Burkman, L.J., Oehninger, S.C., et al. (1989). Hemizona assay using salt-stored human oocytes: evaluation of zona pellucida capacity for binding human spermatozoa. Gamete Res. 22, 1526.CrossRefGoogle ScholarPubMed
Franken, D.R., Coddington, C.C., Burkman, L.J. et al. (1991 a). Defining the valid hemizona assay: accounting for binding variablity within zonae pellucidae and within semen samples from fretile males. Fertil. Steril. 6, 1156–61.CrossRefGoogle Scholar
Franken, D.R., Windt, M.L., Kruger, T.F., et al. (1991 b). Comparison of sperm binding potential of uninseminated, inseminated-unfertilized, and fertilized-noncleaved human oocytes under hemizona assay conditions. Mol. Reprod. Dev. 38, 5661.CrossRefGoogle Scholar
Gwatkin, R.B., Conover, J.C., Collins, R.L. & Quingley, M.M. (1989). Failed fertilization in human in vitro fertilization analyzed with the deoxyribonucleic acid-specific fluorochrome Hoechst 33342. Am. J. Obstet. Gynecol. 168, 135.Google Scholar
Hoshi, K., Tsukikawa, S. & Sato, A. (1991). Importance of Ca2+, K+ and glucose in the medium for sperm penetration through the human zona pellucida. Tohoku J. Exp. Med. 165, 99104.CrossRefGoogle ScholarPubMed
Lanzendorf, S.E., Holmgren, W.J., Johnson, D.E., et al. (1992). Hemizona assay for measuring zona binding in the lowland gorilla. Mol. Reprod. Dev. 31, 264–7.CrossRefGoogle ScholarPubMed
McBride, C.E., Fayrer-Hosken, R.A., et al. (1988). Comparison of rabbit and bovine salt-stored zonae for sperm penetration. J. Androl. 9, 34p (abstract 61).Google Scholar
McNutt, L.L. & Killian, C.J. (1991). Influence of bovine follicular and oviduct fluids on sperm capacitation in vitro. J. Androl. 12, 244–52.CrossRefGoogle ScholarPubMed
Oehninger, S., Scott, R.T., Coddington, C.C., et al. (1989). Validation of the hemizona assay in a monkey model: influence of oocyte maturational stages. Fertil. Steril. 51, 881–5.CrossRefGoogle Scholar
O'Rand, M.G., Herman, B., Diguiseppi, J. (1986). Analysis of deoxyribonucleic acid distribution in noncleaving oocytes from patients undergoing in vitro fertilization. Fertil. Steril. 46, 452–60.CrossRefGoogle ScholarPubMed
Overstreet, J.W., Yanagimachi, R., Katz, D.F., et al. (1980). Penetration of human spermatozoa into the human zona pellucida and the zona-free hamster eggs: a study of fertile donors and infertile patients. Fertil. Steril. 33, 534–42.CrossRefGoogle Scholar
Parrish, J.J., Susko-Parrish, J., Winer, M.A. & First, N.L. (1988). Capacitation of bovine sperm by heparin. Biol. Reprod. 38, 1171–80.CrossRefGoogle ScholarPubMed
Quinn, P., Warnes, G.M., Kerin, J.F., & Kirby, C. (1985). Culture factors affecting the success rate of in vitro fertilization and embryo transfer. Ann. NY Acad. Sci. 442, 195204.CrossRefGoogle ScholarPubMed
Tesarik, J. (1990). Zona pellucida penetrability of metaphase I and II human oocytes after aging and salt treatment. Fertil. Steril. 54, 346–7.CrossRefGoogle ScholarPubMed
Yanagimachi, R. (1988). Mammalian fertilization. In: The physiology of Reproduction, ed. Knobil, E. & Neill, J.D. vol. 1, pp. 135–85. New York: Raven Press.Google Scholar
Yanagimachi, R.Lopata, A., Odom, C.B., et al. (1979). Retention of biologic characteristics of zona pellucida in highly concentrated salt solutions: the use of salt-stored eggs for assessing the fertilizing capacity of spermatozoa. Fertil. Steril. 31, 562–74.CrossRefGoogle ScholarPubMed
Yoshimatsu, N., Yanagimachi, R. & Lopata, A. (1988). Zonae pellucidae of salt-stored hamster and human eggs: their penetrability by homilogous and heterologous spermatozoa. Gamete Res. 21, 115–26.CrossRefGoogle ScholarPubMed