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  4. Differential Development of Rabbit Embryos Derived from Parthenogenesis and Nuclear Transfer
 
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Differential Development of Rabbit Embryos Derived from Parthenogenesis and Nuclear Transfer

Journal
Molecular Reproduction and Development
Journal Volume
68
Journal Issue
1
Pages
58-64
Date Issued
2004
Author(s)
Liu, J.-L.
LI-YING SUNG  
Du, F.
Julian, M.
Jiang, S.
Barber, M.
Xu, J.
Tian, X.C.
Yang, X.
DOI
10.1002/mrd.20045
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-1842532885&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/309968
Abstract
Parthenogenetic development (PA) is often used as a model to investigate activation protocols for nuclear transfer (NT) embryos. The objective of this study was to compare the development, as well as the dynamics of the nuclear materials and microtubules of PA and NT embryos following similar activation treatment. Our results demonstrate that, during parthenogenesis, activation through either electrical pulses or chemical stimulation alone resulted in low cleavage rates and compromised development. A combination of two sets of electrical pulses and a 2-h-exposure to chemical activation medium (5 microg/ml cycloheximide (CHX) and 2 mM 6-dimethylaminopurine (6-DMAP) in KSOM+0.1% BSA) could effectively activate rabbit oocytes, and resulted in a 99% (n = 73) cleavage rate with greater than 60% (n = 73) developing to blastocysts at day 4. However, the same activation protocol following NT resulted in only 65-72% of oocytes cleaved (depending on donor cell type), with less than 20% developing to the blastocyst stage. The differences observed between NT and PA embryos subjected to the same activation protocol were also evident in terms of the time required for their development to the blastocyst stage, as well as the cell numbers present in blastocysts at day 6. Furthermore, laser confocal microscopy revealed that pronuclear formation in the NT embryos was delayed by comparison to that in the parthenotes. In conclusion, our study suggests that an effective protocol for parthenogenesis cannot promise a comparable outcome for NT embryos.
Type
journal article

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