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首页> 外文期刊>Cryobiology: International Journal of Low Temperature Biology and Medicine >Effect of the cryoprotectant concentration on the in vitro embryo development and cell proliferation of OPS-vitrified porcine blastocysts.
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Effect of the cryoprotectant concentration on the in vitro embryo development and cell proliferation of OPS-vitrified porcine blastocysts.

机译:冷冻保护剂浓度对OPS玻璃化猪胚泡的体外胚胎发育和细胞增殖的影响。

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Our objective was to study the effect of the concentration of ethylene glycol (EG) and dimethyl sulfoxide (Me2SO) during vitrification on the development of porcine blastocysts. Vitrification was performed with 0.4 M sucrose and either a Me2SO and EG mixture (15%, 16% and 17% v/v of each) or EG alone (40% v/v), using superfine open pulled straws. Fresh and vitrified blastocysts were cultured for 48 h and the survival and hatching rates were evaluated. Some vitrified and fresh embryos were processed for Hoechst 33342 staining and proliferation cell nuclear antigen (PCNA) inmunolocalization to determine the proliferation index. The survival rate was similar for fresh and vitrified blastocysts, except for blastocysts vitrified using 15% of cryoprotectants, which displayed lower (P < 0.05) survival than fresh blastocysts. Vitrified and fresh blastocysts had a similar cell proliferation index (range: 75.8+/-3.2 to 83.7+/-3). When only hatched blastocysts among groups were compared, the proliferation rate decreased (P < 0.05) after vitrification with 17% of EG-Me2SO. In conclusion, the concentration of EG-Me2SO could be decreased to 16% in the vitrification medium with no reduction of the in vitro developmental ability of the blastocysts. In addition, a 40% EG-based medium can be used for vitrification with similar results to those achieved with a medium containing 16% EG-Me2SO.
机译:我们的目标是研究玻璃化过程中乙二醇(EG)和二甲基亚砜(Me2SO)的浓度对猪胚泡发育的影响。使用超细开放式吸管,用0.4 M蔗糖和Me2SO和EG混合物(每种分别为15%,16%和17%v / v)或单独使用EG(40%v / v)进行玻璃化。将新鲜和玻璃化的胚泡培养48小时,并评估其存活率和孵化率。处理一些玻璃化和新鲜的胚胎,进行Hoechst 33342染色和增殖细胞核抗原(PCNA)的免疫定位,以确定增殖指数。新鲜和玻璃化胚泡的存活率相似,不同的是,使用15%的冷冻保护剂玻璃化的胚泡比新鲜胚泡的存活率低(P <0.05)。玻璃化的和新鲜的胚泡具有相似的细胞增殖指数(范围:75.8 +/- 3.2至83.7 +/- 3)。当仅比较各组中孵化的胚泡时,用17%的EG-Me2SO玻璃化后,增殖速率降低(P <0.05)。总之,在玻璃化培养基中,EG-Me2SO的浓度可以降低至16%,而胚泡的体外发育能力却不会降低。此外,可以使用40%的基于EG的培养基进行玻璃化,其结果与包含16%的EG-Me2SO的培养基所获得的结果相似。

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