Background:At present,vitrification has been widely applied to humans,mice and farm animals.To improve the efficiency of vitrification in straw,bovine oocytes were used to test a new two-step vitrification method in ...Background:At present,vitrification has been widely applied to humans,mice and farm animals.To improve the efficiency of vitrification in straw,bovine oocytes were used to test a new two-step vitrification method in this study.Results:When in vitro matured oocytes were exposed to 20%ethylene glycol(EG20) for 5 min and 40%ethylene glycol(EG40) for 30 s,followed by treatment with 30%glycerol(Gly30),Gly40 or Gly50,a volume expansion was observed in Gly30 and Gly40 but not Gly50.This indicates that the intracellular osmotic pressure after a 30 s differs between EG40 and ranged between Gly40(approximately 5.6 mol/L) and Gly50(approximately 7.0 mol/L).Since oocytes are in EG40 just for only a short period of time(30 s) and at a lower temperature(4℃),we hypothesize that the main function of this step in to induce dehydration.Based on these results,we omitted the EG40 step,before oocytes were pretreated in EG20 for 5 min,exposed to pre-cooled(4℃) Gly50,for 30 s,and then dipped into liquid nitrogen.After warming,81.1%of the oocytes survived,and the surviving oocytes developed into cleavage stage embryos(63.5%) or blastocysts(20.0%) after parthenogenetic activation.Conclusions:These results demonstrate that in a two-step vitrification procedure,the permeability effect in the second step is not necessary.It is possible that the second step is only required to provide adequate osmotic pressure to condense the intracellular concentration of CPAs to a level required for successful vitrification.展开更多
This study was conducted to systematically assess the reproductive performance of transgenic TLR4 ewes.In the TLR4 transgenic founders(F_(0))and their positive offspring(F_(1)),hematological and reproductive parameter...This study was conducted to systematically assess the reproductive performance of transgenic TLR4 ewes.In the TLR4 transgenic founders(F_(0))and their positive offspring(F_(1)),hematological and reproductive parameters and the global DNA methylation level in oocytes at various stages were analyzed.The values of the physiological and biochemical parameters determined from the blood samples did not differ significantly between the transgenic and wild-type ewes.Moreover,the transgenic ewes showed reproductive traits similar to the wildtype ewes.These traits included characteristics of puberty,the estrus cycle,estrus duration,gestation,the pregnancy rate and the superovulation response.Additionally,no significant differences were found between transgenic and wild-type ewes in the DNA methylation level of the oocytes at various stages.In summary,the preliminary evidence presented in this paper demonstrates that the presence of the TLR4 transgene did not affect the reproductive performance in sheep.展开更多
基金supported by the National "863" Project Foundation of China(No.2011AA100303)the National Science and Technology Support Projects of China(No.2011BAD19B01)
文摘Background:At present,vitrification has been widely applied to humans,mice and farm animals.To improve the efficiency of vitrification in straw,bovine oocytes were used to test a new two-step vitrification method in this study.Results:When in vitro matured oocytes were exposed to 20%ethylene glycol(EG20) for 5 min and 40%ethylene glycol(EG40) for 30 s,followed by treatment with 30%glycerol(Gly30),Gly40 or Gly50,a volume expansion was observed in Gly30 and Gly40 but not Gly50.This indicates that the intracellular osmotic pressure after a 30 s differs between EG40 and ranged between Gly40(approximately 5.6 mol/L) and Gly50(approximately 7.0 mol/L).Since oocytes are in EG40 just for only a short period of time(30 s) and at a lower temperature(4℃),we hypothesize that the main function of this step in to induce dehydration.Based on these results,we omitted the EG40 step,before oocytes were pretreated in EG20 for 5 min,exposed to pre-cooled(4℃) Gly50,for 30 s,and then dipped into liquid nitrogen.After warming,81.1%of the oocytes survived,and the surviving oocytes developed into cleavage stage embryos(63.5%) or blastocysts(20.0%) after parthenogenetic activation.Conclusions:These results demonstrate that in a two-step vitrification procedure,the permeability effect in the second step is not necessary.It is possible that the second step is only required to provide adequate osmotic pressure to condense the intracellular concentration of CPAs to a level required for successful vitrification.
基金This study was supported by key special projects for breeding new varieties of genetically engineered organisms in China(2011ZX08011-004).
文摘This study was conducted to systematically assess the reproductive performance of transgenic TLR4 ewes.In the TLR4 transgenic founders(F_(0))and their positive offspring(F_(1)),hematological and reproductive parameters and the global DNA methylation level in oocytes at various stages were analyzed.The values of the physiological and biochemical parameters determined from the blood samples did not differ significantly between the transgenic and wild-type ewes.Moreover,the transgenic ewes showed reproductive traits similar to the wildtype ewes.These traits included characteristics of puberty,the estrus cycle,estrus duration,gestation,the pregnancy rate and the superovulation response.Additionally,no significant differences were found between transgenic and wild-type ewes in the DNA methylation level of the oocytes at various stages.In summary,the preliminary evidence presented in this paper demonstrates that the presence of the TLR4 transgene did not affect the reproductive performance in sheep.