ASSESSMENT OF THE VIABILITY AND PREGNANCY POTENTIAL OF MOUSE EMBRYOS BIOPSIED AT DIFFERENT PREIMPLANTATION STAGES OF DEVELOPMENT

被引:46
作者
KRZYMINSKA, UB [1 ]
LUTJEN, J [1 ]
ONEILL, C [1 ]
机构
[1] ROYAL N SHORE HOSP,HUMAN REPROD UNIT,ST LEONARDS,NSW 2065,AUSTRALIA
关键词
Biopsy; Embryo; Embryo-viability; Micromanipula-tion; Prenatal diagnosis;
D O I
10.1093/oxfordjournals.humrep.a137070
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The developmental potential in vitro and in vivo of preimplantation mouse embryos biopsied at the 4-cell, 8-cell and morula stages were investigated. Biopsy had the least impact when performed at the 8-cell stage. There was no effect of biopsy on the development of 8-cells of blastocysts in vitro (95% compared with 99% of controls) or the implantation rate after transfers (82 versus 87%, P > 0.05); however, fewer embryos (52 versus 71%,P < 0.05) resulted in viable fetuses. There was no effect of biopsy at the 8-cell stage on fetal weight on day 17. Blastocyst formation in vitro was significantly less for 4-cell biopsies compared with their controls (76 versus 90%, P < 0.001) and biopsy also affected the implantation rate (44 versus 59%, P < 0.01). Biopsy was most detrimental when performed on morulae, reducing the implantation rate from 65% for controls to 21% for biopsies (P < 0.001). Fetal viability was also markedly affected with a reduction on day 17 from 42 to 26% accompanied by a significant reduction (24%, P = 0.02) of the mean fetal weight. Handling of embryos for biopsy at the morula stage, which involved removal of the zona pellucida, was a significant but not complete cause of the reduced implantation potential observed (sham-controls and intact-controls: 34 and 65%, P < 0.001), while puncture of the zona during the biopsy of 4-cell and 8-cell embryos had no effect. Therefore, the 8-cell mouse embryo is the most suitable state for embryo biopsy. © 1990 Oxford University Press.
引用
收藏
页码:203 / 208
页数:6
相关论文
共 18 条
  • [1] Fehilly C.G., Willadsen S.M., Embryo manipulation in farm animals, Oxford Rev. Reprod. Biol, 8, pp. 379-413, (1986)
  • [2] Gardner R.L., Edwards R.G., Control of the sex ratio at full term in the rabbit by transferring sexed blastocysts, Nature, 21, (1968)
  • [3] Johnson M.H., The molecular and cellular basis of preimplantation mouse development, Biol. Rev, 56, pp. 463-498, (1981)
  • [4] McGrath J., Solter D., Nuclear transplantation in the mouse by microsurgery and cell fusion, Science, 22, pp. 1300-1302, (1983)
  • [5] McLaren A., Prenatal diagnosis before implantation: Opportunities and problems, Prenatal Diag, 5, pp. 85-90, (1985)
  • [6] Monk M., Handyside A.H., Sexing of preimplantation mouse embryos by measurement of X-linked gene dosage in a single blastomere, J. Reprod. Fertil, 82, pp. 365-368, (1988)
  • [7] Monk M., Handy Side A.H., Hardy K., Whittingham D., Preimplantation diagnosis of deficiency of hypoxanthine phosphoribosyl transferase in a mouse model for Lesch-Nyhan syndrome, Lancet, 2, pp. 423-426, (1987)
  • [8] Monk M., Muggleton-Harris A.L., Rawlings E., Whittingham D.G., Pre-implantation diagnosis of HPRT-deficient male and carrier female mouse embryo by trophectoderm biopsy, Hum. Reprod, 3, pp. 377-381, (1988)
  • [9] Nicolson G.L., Yanagimachi R., Yanagimachi H., Ultrastructural localisation of lectin-binding sites on the zonae pellucidae and plasma membranes of mammalian eggs, J. Cell Biol, 66, pp. 263-274, (1975)
  • [10] Nijs M., Camus M., Van Steirteghem A.C., Evaluation of different biopsy methods of blastomeres from 2-cell mouse embryos, Hum. Reprod, 3, pp. 999-1003, (1988)