
TY  - JOUR
A1  - Feltrin, C. 
A1  - Lima, A. S. 
A1  - Monaco, M. 
A1  - Wilson, S. M. 
A1  - Kim, D. 
A1  - Wheeler, M. B. 
A1  - Rodrigues, J. L. 
T1  - 29 EVALUATION OF DIFFERENT FUSION PARAMETERS IN THE RECONSTRUCTION OF SWINE HANDMADE CLONING EMBRYOS
JF  - Reproduction, Fertility and Development
JO  - Reprod. Fertil. Dev.
Y1  - 2007
VL  - 20
IS  - 1
SP  - 95
EP  - 95
KW  - 
UR  - https://doi.org/10.1071/RDV20N1AB29 
N2  - The goal of this experiment was to compare different fusion parameters in the handmade cloning technique to produce cloned swine embryos. After in vitro maturation of 618 oocytes, 431 (69.8%) presented a visible polar body and were used in the experiment. The next step was the removal of the cumulus oophorus cells and the digestion of the zona pellucida using pronase (5 mg mL&#8211;1) in HEPES TCM199. Oocytes were then exposed to a medium containing cytochalasin B (5 &#181;g mL&#8211;1) for 15 min before being bisected with a hand-held blade. The bisected oocytes (cytoplasts) were then placed in medium supplemented with Hoechst 33342 and exposed to UV light to select cytoplasts without metaphase II plates. Next, two cytoplasts and a mesenchymal stem cell (nucleus donor) were pushed together in a phytohemagglutinin (550 &#181;g mL&#8211;1) solution. Once adhered, these structures were divided into 3 groups (G) to be fused using different parameters: (G1) 2 pulses (DC) of 0.6 kV cm&#8211;1 for 30 &#181;s, (G2) 2 pulses (DC) of 0.9 kV cm&#8211;1 for 30 &#181;s, and (G3) 2 pulses (DC) of 1.2 kV cm&#8211;1 for 30 &#181;s. For all three groups, 0.3 m of mannitol solution (without calcium) was used in the fusion chamber, and an initial pre-pulse (AC) of 10V for 15 s was performed to permit the alignment of 100% of the cytoplast-donor cell structures. After fusion, reconstructed embryos were activated in 0.3 m mannitol and 0.1 mm calcium in the fusion chamber using 2 pulses of 0.9 kV cm&#8211;1 for 30 &#181;s followed by incubation in 10 &#181;g mL&#8211;1 of cycloheximide solution for 4 h. Afterwards, the reconstructed embryos were transferred to NCSU23 medium supplemented with amino acids (nonessential and essential) and 0.4% bovine serum albumin. The embryos were cultured at 39°C in a 100% humidified atmosphere containing 5% CO2, 5% O2, and 90% N2. Cleavage rates were evaluated after 48 h of culture. For G1, the fusion rate was 43% (25/58) with 72% cleavage (18/25), the G2 fusion rate was 87% (56/64) with 80% cleavage (45/56), and the G3 fusion rate was 79% (53/67) with 69% cleavage (37/53). Statistical analysis was performed using the chi-square test. There were no significant differences in fusion rates between groups G2 and G3, but the fusion rate of these groups was significantly different from that of G1 (P < 0.05). No significant differences in cleavage rate were observed among the three groups. In conclusion, fusion using 2 pulses at either 0.9 or 1.2 kV cm&#8211;1 for 30 &#181;s was more efficient for embryo reconstruction in the handmade cloning technique compared to that using 2 pulses at 0.6 kV cm&#8211;1 for 30 &#181;s. Further studies need to be performed to improve cleavage rates and assess development to the blastocyst stage. 
ER  -

