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In vitro ageing of pig oocytes: effects of the histone deacetylase inhibitor trichostatin A

Published online by Cambridge University Press:  01 May 2008

M. Ješeta
Affiliation:
Faculty of Agrobiology, Food and Natural Resources, Department of Veterinary Sciences, University of Agriculture in Prague, Prague, Czech Republic.
J. Petr
Affiliation:
Research Institute of Animal Production, Prague, Czech Republic.
T. Krejčová*
Affiliation:
Department of Veterinary Science, Czech University of Agriculture in Prague, 165 21, Kamýcká 129, Prague 6, Czech Republic. Faculty of Agrobiology, Food and Natural Resources, Department of Veterinary Sciences, University of Agriculture in Prague, Prague, Czech Republic.
E. Chmelíková
Affiliation:
Faculty of Agrobiology, Food and Natural Resources, Department of Veterinary Sciences, University of Agriculture in Prague, Prague, Czech Republic.
F. Jílek
Affiliation:
Faculty of Agrobiology, Food and Natural Resources, Department of Veterinary Sciences, University of Agriculture in Prague, Prague, Czech Republic.
*
All correspondence to: Tereza Krejčová. Department of Veterinary Science, Czech University of Agriculture in Prague, 165 21, Kamýcká 129, Prague 6, Czech Republic. Tel.: +420 224382931. Fax: +420 234381841. e-mail: [email protected]

Summary

After in vitro maturation, the unfertilized pig oocytes underwent the process called ageing. This process involves typical events such as fragmentation, spontaneous parthenogenetic activation or lysis. Inhibition of histone deacetylase, using its specific inhibitor trichostatin A (TSA), significantly delayed the maturation of pig oocytes cultured in vitro. The ageing of oocytes matured under the effect of TSA is the same as the ageing in oocytes matured without TSA. The inhibition of histone deacetylase during oocyte ageing significantly reduced the percentage of fragmented oocytes (from 30% in untreated oocytes to 9% in oocytes aged under the effect of 100 nM of TSA). Oocytes matured in vitro and subsequently aged for 1 day under the effects of TSA retained their developmental capacity. After parthenogenetic activation, a significantly higher portion (27% vs. 15%) of oocytes developed to the blastocyst stage after 24 h ageing under 100 nM TSA when compared with oocytes activated after 24 h ageing in a TSA-free medium. The parthenogenetic development in oocytes aged under TSA treatment is similar to the development of fresh oocytes (29% of blastocyst) artificially activated immediately after in vitro maturation.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2008

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