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Reproduction (2005) 130 351-357
DOI: 10.1530/rep.1.00644
Copyright © 2005 Society for Reproduction and Fertility
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RESEARCH

Caffeine promotes premature chromosome condensation formation and in vitro development in porcine reconstructed embryos via a high level of maturation promoting factor activity during nuclear transfer

Manabu Kawahara, Takuya Wakai, Ken-Ichi Yamanaka, Jin Kobayashi1, Satoshi Sugimura, Takashi Shimizu, Hiromichi Matsumoto, Jin-Hoi Kim2, Hiroshi Sasada and Eimei Sato

Laboratory of Animal Reproduction, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555, Japan, 1 Research Farm, Miyagi Agricultural College, Sendai, Japan and 2 Division of Applied Life Science, GyeongSang National University, Chinju, GyeongNam, Korea

Correspondence should be addressed to M Kawahara, Department of Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagayaku, Tokyo 156-8502, Japan; Email: mana1976{at}nodai.ac.jp

When the nucleus in G0/G1 phase is transferred to an enucleated oocyte by nuclear transfer (NT), its nuclear envelope is broken, followed by condensation of chromosome structure by maturation promoting factor (MPF). This morphological remodeling of the transferred interphase nucleus seems to be essential for subsequent development of NT embryos. In this study, we treated porcine NT embryos with caffeine, which has been reported to increase MPF activity, to keep their MPF level high during NT. When 2.5 mM caffeine was added to the handling medium, the proportion of NT embryos showing condensed chromosome increased significantly (P < 0.05). In NT embryos treated with caffeine, the activity of p34cdc2 kinase was significantly (P < 0.05) higher than in those without caffeine at 3 h post-injection. In addition, the rate of development to the blastocyst stage after activation was significantly (P < 0.05) higher in NT embryos treated with caffeine. These results indicate that caffeine treatment can increase not only the rate of chromosome condensation but also the developmental rate to the blastocyst stage of porcine NT embryos. This action is most likely due to the support/increase of MPF activity throughout the process of NT.







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