Comparison of two co-culture systems to assess the survival of in vitro produced bovine blastocysts after vitrification

The ability of bovine blastocysts to recover after cryopreservation and thawing procedures is often assessed by evaluating their re-expansion during in vitro co-culture. However, the influence of factors such as feeder cell type and gas atmosphere on blastocyst survival and evolution have never been considered. This study therefore compared two cell co-culture systems and two different gas atmospheres to assess survival of in vitro produced bovine blastocysts after vitrification. Day-7 blastocysts (n = 181) were vitrified in a mixture of 25% glycerol/25% ethylene glycol. After warming and dilution, they were co-cultured either on Buffalo rat liver cells (BRL CC cell line) or on granulosa cells (GR CC primary culture) in TCM 199 supplemented with 10% FCS and under an atmosphere of 5% or 20% O-2. Surviving and hatching rates were recorded at 24 h intervals for 3 days. After 72 h of culture, surviving blastocysts were treated for differential counting of inner cell mass (ICM) and trophectoderm cells. Blastocyst survival rates were higher when BRL and granulosa co-culture were performed under 20% oxygen as compared to 5% oxygen (20% O-2: 62% vs. 5% O-2: 25%, P < 0.0001). However, the quality of blastocysts surviving in the granulosa co-culture condition was lower under 20% O-2 than under 5% O-2 as indicated by lower total and trophectoderm cell numbers (respectively 79 +/- 6 and 56 +/- 6 at 20% O-2 vs. 100 +/- 10 and 74 +/- 10 at 5% O-2, P < 0.05), by an altered ICM/trophectoderm ratio (20% O-2: 28% vs. 5% O-2: 23%, P < 0.05), by a higher total nuclear fragmentation (20% O-2: 13.7% vs. 5% O-2: 1.5%. P < 0.05) and a trend to decreased hatching (20% O-2: 32% vs. 5% O-2: 81%, P = 0.07). Whereas, for BRL co-culture, 20% O-2 yielded higher quality blastocysts than 5% O-2 as evaluated by higher ICM and trophectoderm cell numbers (19 +/- 1 and 71 +/- 5 at 20% O-2 vs. 15 +/- 2 and 48 +/- 9 at 5% O-2, respectively, P < 0.05), by lower nuclear fragmentation in the ICM (20% O-2: 2.2% vs. 5% O-2: 6.7%, P < 0.05). In conclusion, co-culture conditions may influence blastocysts survival and quality after cryopreservation. In our conditions, co-culture with BRL cells under 20% O-2 seems to be the best combination to evaluate blastocyst survival and quality after vitrification. (C) 1998 Elsevier Science B.V. All rights reserved.