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Human Reproduction, Vol. 7, No. 8, pp. 1144-11499, 1992
© 1992 European Society of Human Reproduction and Embryology


other

Improved development of human embryos in vitro by a human oviductal cell co-culture system*

W.S.B. Yeung1,3, P.C. Ho1, E.Y.L. Lau1 and S.T.H. Chan2

1Department of Obstetrics and Gynaecology, University of Hong Kong 2Department of Zoology, University of Hong Kong

Correspondence: 3To whom correspondence should be addressed at: Department of Obstetrics and Gynaecology, University of Hong Kong, Queen Mary Hospital, Hong Kong

This study was undertaken to determine the effect of co-culture with human oviductal cells on human embryos. Spare embryos from gamete intra-Fallopian transfer (GIFT), pronuclear stage transfer (PROST) and in-vitro fertilization/embryo transfer (TVF/ET) programmes were either cultured in serum-supplemented Earle's balanced salt solution alone, or co-cultured in the same solution with oviductal cells from the pronuclear stage (day 1 post-insemination) or two-to four-cell stage (day 2 post-insemination). The co-cultured embryos appeared to have a higher developmental potential (higher rate of blastocyst formation and lower fragmentation rate), although there was no statistical difference in their rate of development, degree of fragmentation and stages attained, when compared with conventionally cultured embryos. The percentage of hatching blastocysts was significantly higher (P < 0.05, Fisher's exact test) for embryos co-cultured from day 1 post-insemination (38%) than for embryos which had not been co-cultured (7%). The blastocyst hatching rate for embryos co-cultured from day 2 post-insemination was 15%. It was therefore concluded that co-culture of human embryos with oviductal cells could improve the development of the embryos in vitro. The degree of improvement was more pronounced when the co-culture started at an earlier stage.

Key words: co-culture/embryo development/oviduct


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