Browse > Article

Effect of Kinetin on In Vitro Development of Parthenogenetic Porcine Oocytes Exposed to Demecolcine Prior to Activation  

Kim, Ki-Young (Laboratory of Embryo Biotechnology and Cellular Reprogramming, Dental Research Institute and BK2I CLS, Seoul National University School of Dentistry)
Park, Sang-Kyu (Laboratory of Embryo Biotechnology and Cellular Reprogramming, Dental Research Institute and BK2I CLS, Seoul National University School of Dentistry)
Roh, Sang-Ho (Laboratory of Embryo Biotechnology and Cellular Reprogramming, Dental Research Institute and BK2I CLS, Seoul National University School of Dentistry)
Publication Information
Journal of Embryo Transfer / v.24, no.2, 2009 , pp. 105-108 More about this Journal
Abstract
This study was designed to investigate the effect of kinetin on in vitro development of parthenogenetic porcine oocytes exposed to demecolcine prior to activation. In vitro matured metaphase II stage oocytes were incubated in 0 or 2 ${\mu}$g/ml demecolcine supplemented defined culture medium for 3 h and the oocytes were activated electrically. The parthenogenetic porcine embryos were then cultured in 0 or 200 ${\mu}$M kinetin supplemented defined culture medium for 7 days. Regardless of demecolcine treatment, kinetin supplementation increased blastocyst rates significantly (7.0% versus 12.1% and 4.9% versus 8.5%; Control versus Kinetin and Demecolcine versus Kinetin + Demecolcine, respectively, p<0.05). Demecolcine treatment before activation tended to decrease blastocyst rates regardless of kinetin supplementation although it is not statistically significant. Total cell numbers in the blastocysts also tended to be elevated in embryos when supplemented with kinetin, however only the result between Kinetin and Demecolcine groups is statistically significant (37.6 ${\times}$ 7.2 versus 28.1 ${\times}$ 9.5, respectively, p<0.05). In conclusion, the present report shows that kinetin enhances developmental competence of parthenogenetic porcine embryo regardless of demecolcine pre-treatment before parthenogenetic activation when they were developed in defined culture condition.
Keywords
kinetin; demecolcine; porcine embryo; in vitro culture; parthenogenesis;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Francis D and Sorrell DA. 2001. The interface between the cell cycle and plant growth regulators: A mini review. Plant Growth Regul. 33:1-12   DOI   ScienceOn
2 Miller CO, Skoog F, von Saltza MH and Strong FM. 1955. Kinetin, a cell division factor from deoxyribonucleic acid. J. Am. Chem. Soc. 77:1329-1334
3 Tani T, Shimada H, Kato Y and Tsunoda Y. 2006. Demecolcine-assisted enucleation for bovine cloning. Cloning Stem Cells 8:61-66   DOI   ScienceOn
4 Rieder CL and Palazzo RE. 1992. Colcemid and the mitotic cycle. J. Cell. Sci. 102(3):387-392
5 Yin XJ, Kato Y and Tsunoda Y. 2002a. Effect of enucleation procedures and maturation conditions on the development of nuclear-transferred rabbit oocytes receiving male fibroblast cells. Reproduction 124:41-47   DOI   PUBMED   ScienceOn
6 Gasparrini B, Gao S, Ainslie A, Fletcher J, McGarry M, Ritchie WA, Springbett AJ, Overstrom EW, Wilmut I and De Sousa PA. 2003. Cloned mice derived from embryonic stem cell karyoplasts and activated cytoplasts prepared by induced enucleation. BioI. Reprod. 68:1259-1266   DOI   ScienceOn
7 Olsen A, Siboska GE, Clark BF and Rattan SI. 1999. N(6)-Furfuryladenine, kinetin, protects against Fenton reaction-mediated oxidative damage to DNA. Biochem. Biophys. Res. Commun. 265:499-502   DOI   ScienceOn
8 Bayliss M. 1985. Control of cell division in cultured cells. In:Bryant JA, Francis D, editors. The Cell Division Cycle in Plants., Cambridge University Press, Cambridge, pp. 157-178
9 Barciszewski J, Siboska GE, Pedersen BO, Clark BF and Rattan SI. 1997. A mechanism for the in vivo formation of $N^6$-furfuryladenine, kinetin, as a secondary oxidative damage product of DNA. FEBS Lett. 414:457-460   DOI   ScienceOn
10 Rattan SI and Clark BF. 1994. Kinetin delays the onset of ageing characteristics in human fibroblasts. Biochem. Biophys. Res. Commun. 201:665-672   DOI   ScienceOn
11 Won C, Park SK, Cho SG, Min BM and Roh S. 2008. Kinetin enhances in vitro development of parthenogenetic and nuclear transfer porcine embryos. Mol. Reprod. Dev. 75:1701-1709   DOI   ScienceOn
12 Miller CO, Skoog F, Okumura FS, von Saltza MH and Strong FM. 1956. Isolation, structure and synthesis of kinetin, a substance promoting cell division. J. Am. Chem. Soc. 78:1375-1380   DOI
13 Rodriguez-Arnaiz R, Sortibran AC and Tellez GO. 2004. Detection of mitotic recombination and sex chromosome loss induced by adriamycin, chlorambucil, demecolcine, paclitaxel and vinblastine in somatic cells of Drosophila melanogaster in vivo. Mutagenesis 19:121-127   DOI   ScienceOn
14 Yin XJ, Tani T, Yonemura I, Kawakami M, Miyamoto K, Hasegawa R, Kato Y and Tsunoda Y. 2002b. Production of cloned pigs from adult somatic cells by chemically assisted removal of maternal chromosomes. BioI. Reprod. 67:442-446   DOI   ScienceOn
15 Sheu JR, Hsiao G, Shen MY, Chou CY, Lin CH, Chen TF and Chou DS. 2003. Inhibitory mechanisms of kinetin, a plant growth-promoting hormone, in platelet aggregation. Platelets. 14:189-196   DOI   ScienceOn