
%0 Journal Article
%A Du, Y. 
%A Kragh, P. M. 
%A Zhang, X. 
%A Yang, H. 
%A Vajta, G. 
%A Bolund, L. 
%T 90 SUCCESSFUL VITRIFICATION OF PARTHENOGENETIC PORCINE BLASTOCYSTS PRODUCED FROM DELIPATED <i>IN VITRO</i>-MATURED OOCYTES
%J Reproduction, Fertility and Development
%D 2005/12/14
%V 18
%N 2
%P 153-153
%K 
%R https://doi.org/10.1071/RDV18N2AB90
%U https://www.publish.csiro.au/paper/RDV18N2AB90 
%X Cryopreservation of cloned porcine embryos may improve the output of somatic cell cloning considerably by alleviating logistic problems. However, the high lipid content of porcine oocytes and embryos compromises their cryotolerance. Recently a noninvasive procedure was published for delipation of porcine embryos with centrifugation but without subsequent micromanipulation (Esaki et al. 2004 Biol. Reprod. 71, 432-436). This method was applied to our present work with few modifications to compare the cryosurvival of porcine blastocysts produced from delipated vs. intact oocytes with parthenogenetic activation. In four replicates, a total of 192 oocytes were used for the experiments. After in vitro maturation for 44 h, cumulus cells were removed and oocytes were randomly distributed into two groups. For delipation, oocytes were digested with 1 mg/mL pronase in the presence of 50% cattle serum (CS) for 3 min, and washed in HEPES-buffered TCM-199 medium supplemented with 20% CS. Subsequently, 40-50 oocytes were centrifuged (12 000g, 20 min) in HEPES-buffered TCM-199 medium supplemented with 2% CS, 3 mg/mL polyvinyl alcohol and 7.5 ¼g/mL cytochalasin B (CB). Zonae pellucidae of both centrifuged and intact oocytes were removed completely by further digestion in 2 mg/mL pronase solution. For activation, a single direct current of 85 kV/cm for 80 ¼s was applied to both groups, followed by 4-h treatment with 5 ¼g/mL CB and 10 ¼g/mL cycloheximide. All embryos were then cultured in modified NCSU37 medium. Day 7 blastocysts were vitrified and warmed by using the Cryotop technique (Kuwayama et al. 2005 RBM Online 11, 300-308) at 38.5°C. Survival of vitrified blastocysts was determined according to re-expansion rates after 24 h recovery in culture medium supplemented with 10% CS. Cell numbers of reexpanded blastocysts from both groups were determined after Hoechst staining. Results were compared by ANOVA. Partial zona digestion and centrifugation resulted in successful delipation in 173/192 (90%) of oocytes. The development to blastocysts was not different between delipated and intact oocytes (28 ± 7% vs. 28 ± 5%, respectively; P > 0.05). However, survival rates of blastocysts derived from delipated oocytes were significantly higher than those developed from intact oocytes (85 ± 6% vs. 32 ± 7%, respectively; P < 0.01). There was no difference in average cell number of re-expanded blastocysts derived from either delipated or intact oocytes (36 ± 7 vs. 38 ± 9, respectively; P > 0.05). Our results prove that the simple delipation technique does not hamper the in vitro developmental competence of activated porcine oocytes, and improves the cryosurvival of the derived blastocysts without significant loss in cell number. Future investigations are required to prove the value of the method in an analogue system with blastocysts produced by somatic cell nuclear transfer. 
