Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-10T15:30:54.978Z Has data issue: false hasContentIssue false

Distribution of cortical granules in bovine oocytes classified by cumulus complex

Published online by Cambridge University Press:  26 September 2008

M. Hosoe*
Affiliation:
National Institute of Animal Industry, Tsukuba, Japan.
Y. shioya
Affiliation:
National Institute of Animal Industry, Tsukuba, Japan.
*
Misa Hosoe, National Institute of Animal Industry, Tsukuba Norindanchi P.O. Box 5, Ibaraki 305, Japan. Telephone: +81-298-38-8636. Fax: +81-298-38-8606.

Summary

The present study was conducted to examine distributional changes of cortical granules(CGs)during meitotic maturation and fetilisation in vitro and the developmental ability in bovine oocytes classified by cumulus cells. The oocytes were classified by the morphology if their cumulus cell layers as follows: class A, compact and thick; class B, compact but thin; class C, naked; and class D, expanded. some of the oocytes were stained with Lens curinalis agglutinin(LCA) before and after maturation in vitro and after insemination, and then stained with orcein to observe their nuclear stages. The others were left in culture. Distributional patterns of the CGs were classified into four types: type I, CGs distributed in clusters; type II, CGs dispersed and partly clustered; type III, all CGs dispersed; and type IV, no CGs Most of the oocytes before culture showed a type I pattern, but this decreased after maturation culture, whereas type III increased in class A. The oocytes of class B showed similar changes while the oocytes of class C did not. In class C, many oocytes showed type I after culture indicating that cytoplasmic maturation was not completed. IN class D, 80.4% of the oocytes exhibited types III before maturation culture, indicating that their cytoplasmic maturation was different from classes A–C. and about 70% of the class D oocytes were at the unclear stage of germinal vesicle breakdown(GVBD) before culture. The developmental rates to blastocysts in classes A–D were 28.7%, 23.1%, 0.5% and 3.4% respectively.

Type
Article
Copyright
Copyright © Cambridge University Press 1997

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Assay, R.J., Hyttel, P., Greve, T. & Purwantara, B. (1994). Oocyte morphology in dominant and subordinate follicles. Mol. Reprod. Dev. 7, 335–44.CrossRefGoogle Scholar
Blondin, P. & Sirard, M.-A. (1995). Oocyte and follicular morphology as determining characteristics for developmental competence in bovine oocytes. Mol. Reprod. Dev. 41, 5462.CrossRefGoogle ScholarPubMed
Brackett, B.G. & Oliphant, G. (1975). Capacitation of rabbit spermatozoa in vitro. Biol. Reprod. 12, 260–74.CrossRefGoogle ScholarPubMed
Cherr, G.N., Drobnis, E.Z. & Katz, D.F. (1988). Localization of cortical granule constituents before and after exocytosis in the hamster egg. J. Exp. Zool. 246, 8193.CrossRefGoogle ScholarPubMed
Cran, D.G. & Esper, C.R. (1990). Cortical granules and the cortical reaction in mammals. J. Reprod. Fertil. Suppl. 42, 177–88.Google ScholarPubMed
de Loos, F., van Vilet, C., van Maurik, P. & Kruip, T.A.M. (1989). Morphology of immature bovine oocytes. Gamete Res. 24, 197204.CrossRefGoogle ScholarPubMed
de Loos, F., van Maurik, P., van Beneden, T. & Kruip, T.A.M. (1992). Structural aspects of bovine oocyte maturation in vitro. Mol. Reprod. Dev. 31, 208–14.CrossRefGoogle ScholarPubMed
Ducibella, T., Anderson, E., Albertini, D.F., Aalberg, J. & Rangarajan, S. (1988). Quantitative studies of changes in cortical granule number and distribution in the mouse oocyte during meiotic maturation. Dev. Biol. 130, 184–97.CrossRefGoogle ScholarPubMed
Fukui, Y. & Sakuma, Y. (1980). Maturation of bovine oocytes cultured in vitro: relation to ovarian activity, follicular size and the presence or absence of cumulus cells. Biol. Reprod. 22, 669–73.CrossRefGoogle ScholarPubMed
Hazeleger, N.L., Hill, D.J., Stubbings, R.B. & Walton, J.S. (1995). Relationship of morphology and follicular fluid environment of bovine oocytes to their developmental potential in vitro. Theriogenology 43, 509–22.CrossRefGoogle ScholarPubMed
Hyttel, P., Xu, K.P., Smith, S. & Greve, T. (1986). Ultrastructure of in-vitro oocyte maturation in cattle. J. Reprod. Fertil. 78, 615–25.CrossRefGoogle ScholarPubMed
Kastrop, P.M.M., Bevers, M.M., Destree, O.H.J. & Kruip, T.A.M. (1990). Analysis of protein synsesis in morphologically classified bovine follicular oocytes before and after maturation in vitro. Mol. Reprod. Dev. 26, 222–6.CrossRefGoogle ScholarPubMed
Kruip, T.A.M., Cran, D.G., van Beneden, T.H. & Dieleman, S.J. (1983). Structural changes in bovine oocytes during final maturation in vivo. Gamete Res. 8, 2947.CrossRefGoogle Scholar
Leibfried, L. & First, N.L. (1979). Characterization of bovine follicular oocytes and their ability to mature in vitro. J. Anim. Sci. 8, 7686.CrossRefGoogle Scholar
Leibfried-Rutledge, M.L., Critser, E.S., Eyestone, W.H., Northey, D.L. & First, N.L. (1987). Development potential of bovine oocytes matured in vitro or in vivo. Biol. Reprod. 36, 376–83.CrossRefGoogle ScholarPubMed
Madison, V., Avery, B. & Greve, T. (1992). Selection of immature bovine oocytes for developmental potential in vitro. Anim. Reprod. Sci. 27, 111.CrossRefGoogle Scholar
Niimura, S. & Hosoe, M. (1995). Changes in cortical granule distribution within bovine oocytes during maturation and fertilization in vitro. J. Reprod. Dev. 41, 103–8.CrossRefGoogle Scholar
Tervit, H.R., Whittigham, D.G. & Rowson, L.E.A. (1972). Successful culture in vitro of sheep and cattle ova. J. Reprod. Fertil. 30, 493–7.CrossRefGoogle ScholarPubMed
Sathansanthan, A.H. & Trounson, A.O. (1982). Ultrastructural observations on cortical granules in human follicular oocytes. Gamete Res. 5, 191–8.CrossRefGoogle Scholar
Shioya, Y., Kuwayama, M., Fukushima, M., Iwasaki, S. & Hanada, A. (1988). In vitro fertilization and cleavage capability of bovine follicular oocytes classified by cumulus cells and matured in vitro. Theriogenology 30, 489–96.CrossRefGoogle ScholarPubMed
Yoshida, M., Cran, D.G. & Persel, V.G. (1993). Confocual and fluorescence microscopic study using lectins of the distribution of cortical granules during the maturation and fertilization of pig oocytes. Mol. Reprod. Dev. 36, 462–8.CrossRefGoogle Scholar