In vitro and in vivo developmental potential of nuclear transfer embryos using bovine cumulus cells prepared in four different conditions

Cloning Stem Cells. 2003;5(2):101-8. doi: 10.1089/153623003322234696.

Abstract

We examined the effect of culture of donor cells on nuclear transfer efficiency using bovine cumulus cells treated with four different conditions: (1). group A, the cells removed from cumulus-oocyte complexes (COC) after aspiration of ovarian follicles; (2). group B, the cells removed from COC after in vitro maturation; (3). group C, the cells cultured in Dulbecco's Modified Eagle's Medium (DMEM) with 10% fetal bovine serum (FBS) for 3 days after some subculture; and (4). group D, the cells cultured in DMEM with 0.5% FBS for an additional 5 days. Analysis of cell cycle using flow cytometry revealed that the relative proportion of donor cells at G0/G1 phase of cell cycle was 89.7% in group A, 89.5% in group B, 76.0% in group C, and 90.6% in group D. The developmental rates to blastocyst stage in groups C (45.3%) and D (46.4%) were significantly (p < 0.05) higher than in groups A (17.5%) and B (31.9%). After transfer of blastocysts produced in each group, nine of 24 recipients became pregnant on day 30. A total of five live calves were obtained from cumulus cells in all groups (group A [n = 1], group B [n = 1], group C [n = 2], and group D [n = 1]).

Publication types

  • Comparative Study
  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle*
  • Cell Culture Techniques / methods*
  • Cell Cycle
  • Cells, Cultured
  • Cloning, Organism / methods*
  • Culture Media, Conditioned
  • Embryo Transfer
  • Embryonic and Fetal Development*
  • Female
  • Nuclear Transfer Techniques*
  • Oocytes
  • Ovarian Follicle / cytology
  • Pregnancy
  • Time Factors

Substances

  • Culture Media, Conditioned