Viability of cloned bovine embryos after one or two cycles of nuclear transfer and in vitro culture

F J Ectors; A Delval; L C Smith; K Touati; B Remy; J F Beckers; F Ectors

doi:10.1016/0093-691x(95)00280-l

Viability of cloned bovine embryos after one or two cycles of nuclear transfer and in vitro culture

Theriogenology. 1995 Nov;44(7):925-33. doi: 10.1016/0093-691x(95)00280-l.

Authors

F J Ectors¹, A Delval, L C Smith, K Touati, B Remy, J F Beckers, F Ectors

Affiliation

¹ Department of Animal Endocrinology and Reproduction, Faculty of Veterinary Medicine, University of Liege, B-4000 Liege, Belgium.

PMID: 16727788
DOI: 10.1016/0093-691x(95)00280-l

Abstract

We described an exclusively in vitro procedure for cloning and recloning bovine embryos. Embryos obtained by IVM/IVF/IVC developed to the morula stage were used as blastomere donors in cunjunction with IVM recipient oocytes. Reconstructed embryos were developed in vitro in co-culture using bovine oviductal epithelial cells. The resulting morulae were used as donors for recloning under the same experimental conditions. No significant difference was observed between cloning and recloning in terms of development (rates of blastocysts: 12.9 versus 14.9%), in the number of nuclei per blastocyst (63.8 versus 49.1), or in pregnancy rates (35.7 versus 33.3%). The high variability observed between replicates and the correlation between results in first and second cycle nuclear transfer may suggest an inherant potential of individual donor embryos to support development by cloning.