Artificial activation of bovine and equine oocytes with cycloheximide, roscovitine, strontium, or 6-dimethylaminopurine in low or high calcium concentrations

Summary Knowledge on parthenogenetic activation of oocytes is important to improve the efficiency of nuclear transfer (NT) and intracytoplasmic sperm injection (ICSI) because artificial activation of oocyte (AOA) is an essential step to achieve embryo production. Although different procedures for AOA have been established, the efficiency of in vitro production of embryos remains low, especially in equines and Bos taurus bovines. In an attempt to improve the techniques of NT and ICSI in bovine and equine species, we tested different combinations of drugs that had different mechanisms of action for the parthenogenetic activation of oocytes in these animals. The oocytes were collected, in vitro matured for 24 to 30 h and activated artificially, in the presence of low or high concentrations of calcium, with combinations of calcium ionophore (ionomycin) with cycloheximide, roscovitine, strontium, or 6-dimethylaminopurine (6-DMAP). For assessment of activation rates, oocytes were stained with Hoechst 33342 and observed under an inverted microscope. We showed that all combinations of drugs were equally efficient in activating bovine oocytes, with the best results obtained when high concentrations of calcium were adopted. For equine oocytes, high concentrations of calcium were not beneficial for the parthenogenetic activation and the combination of ionomycin with either 6-DMAP or roscovitine was effective in inducing artificial activation of oocytes. We believe that our preliminary findings provide some clues for the development of a better AOA protocol to be used with these species.

[1]  Y. H. Choi,et al.  In vitro-produced equine embryos: production of foals after transfer, assessment by differential staining and effect of medium calcium concentrations during culture. , 2007, Theriogenology.

[2]  R. Duchi,et al.  Developmental competence of equine oocytes and embryos obtained by in vitro procedures ranging from in vitro maturation and ICSI to embryo culture, cryopreservation and somatic cell nuclear transfer. , 2007, Animal reproduction science.

[3]  K. Swann,et al.  PLCzeta, a sperm-specific PLC and its potential role in fertilization. , 2007, Biochemical Society symposium.

[4]  Y. H. Choi,et al.  Production of horse foals via direct injection of roscovitine-treated donor cells and activation by injection of sperm extract. , 2006, Reproduction.

[5]  D. Varner,et al.  Blastocyst development in equine oocytes with low meiotic competence after suppression of meiosis with roscovitine prior to in vitro maturation , 2006, Zygote.

[6]  S. C. Méo,et al.  Use of strontium for bovine oocyte activation. , 2005, Theriogenology.

[7]  T. Horiuchi,et al.  Evaluation of activation treatments for blastocyst production and birth of viable calves following bovine intracytoplasmic sperm injection. , 2005, Animal reproduction science.

[8]  M. Ensslin,et al.  Mammalian fertilization , 2004, Current Biology.

[9]  S. C. Méo,et al.  Activation and early parthenogenesis of bovine oocytes treated with ethanol and strontium. , 2004, Animal reproduction science.

[10]  M. Kurokawa,et al.  Intracellular calcium oscillations and activation in horse oocytes injected with stallion sperm extracts or spermatozoa. , 2003, Reproduction.

[11]  Y. H. Choi,et al.  Effects of roscovitine on maintenance of the germinal vesicle in horse oocytes, subsequent nuclear maturation, and cleavage rates after intracytoplasmic sperm injection. , 2003, Reproduction.

[12]  F. Aoki,et al.  Acquisition of transcriptional competence in the 1‐cell mouse embryo: Requirement for recruitment of maternal mRNAs , 2003, Molecular reproduction and development.

[13]  G. Vajta,et al.  Handmade Somatic Cell Cloning in Cattle: Analysis of Factors Contributing to High Efficiency In Vitro1 , 2003, Biology of reproduction.

[14]  D. B. Carter,et al.  Transgenic swine for biomedicine and agriculture. , 2003, Theriogenology.

[15]  F. A. Lai,et al.  PLC zeta: a sperm-specific trigger of Ca(2+) oscillations in eggs and embryo development. , 2002, Development.

[16]  K. White,et al.  Cloned mule pregnancies produced using nuclear transfer , 2002 .

[17]  G. Anderson,et al.  Influence of Insulin-Like Growth Factor-I and Its Interaction with Gonadotropins, Estradiol, and Fetal Calf Serum on In Vitro Maturation and Parthenogenic Development in Equine Oocytes1 , 2001, Biology of reproduction.

[18]  P. Mermillod,et al.  Effects of cell cycle dependent kinases inhibitor on nuclear and cytoplasmic maturation of porcine oocytes , 2001, Molecular reproduction and development.

[19]  J. Parys,et al.  Down-regulation of the inositol 1,4,5-trisphosphate receptor in mouse eggs following fertilization or parthenogenetic activation. , 2000, Developmental biology.

[20]  J. Bodart,et al.  Differential effects of 6-DMAP, olomoucine and roscovitine on Xenopus oocytes and eggs. , 2000, Zygote.

[21]  P. Mermillod,et al.  High developmental competence of cattle oocytes maintained at the germinal vesicle stage for 24 hours in culture by specific inhibition of MPF kinase activity , 2000, Molecular reproduction and development.

[22]  L. Liu,et al.  Interplay of maturation-promoting factor and mitogen-activated protein kinase inactivation during metaphase-to-interphase transition of activated bovine oocytes. , 1999, Biology of reproduction.

[23]  J. Mizuno,et al.  Intracellular calcium responses in bovine oocytes induced by spermatozoa and by reagents. , 1998, Theriogenology.

[24]  P. Loi,et al.  Development of parthenogenetic and cloned ovine embryos: effect of activation protocols. , 1998, Biology of reproduction.

[25]  Roger Y. Tsien,et al.  Cell-permeant caged InsP3 ester shows that Ca2+ spike frequency can optimize gene expression , 1998, Nature.

[26]  Christopher C. Goodnow,et al.  Differential activation of transcription factors induced by Ca2+ response amplitude and duration , 1997, Nature.

[27]  D. Whittingham,et al.  Meiotic and mitotic Ca2+ oscillations affect cell composition in resulting blastocysts. , 1997, Developmental biology.

[28]  B. N. Day,et al.  Microtubule organization in porcine oocytes during fertilization and parthenogenesis. , 1996, Biology of reproduction.

[29]  R. Schultz,et al.  Cycloheximide-induced activation of mouse eggs: effects on cdc2/cyclin B and MAP kinase activities. , 1996, Journal of cell science.

[30]  K. White,et al.  Intracellular receptors and agents that induce activation in bovine oocytes , 1996 .

[31]  D. Whittingham,et al.  Cytogenetical analysis and developmental potential of vitrified mouse oocytes. , 1995, Biology of reproduction.

[32]  S. Homa Calcium and meiotic maturation of the mammalian oocyte , 1995, Molecular reproduction and development.

[33]  K. Hinrichs,et al.  Activation of Horse Oocytes , 1995 .

[34]  X. Yang,et al.  Nuclear dynamics of parthenogenesis of bovine oocytes matured in vitro for 20 and 40 hours and activated with combined ethanol and cycloheximide treatment , 1994, Molecular reproduction and development.

[35]  J T Kline,et al.  Repetitive calcium transients and the role of calcium in exocytosis and cell cycle activation in the mouse egg. , 1992, Developmental biology.

[36]  J. D. Neill,et al.  The Physiology of reproduction , 1988 .

[37]  P. Cobbold,et al.  Free Ca2+ increases in exponential phases during mouse oocyte activation , 1981, Nature.