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Aggregation of cloned embryos in empty zona pellucida improves derivation efficiency of pig ES-like cells

机译:空的透明带中克隆胚胎的聚集提高了猪ES样细胞的衍生效率

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The development of embryonic stem cells (ESCs) from large animal species has become an important model for therapeutic cloning using ESCs derived by somatic cell nuclear transfer (SCNT). However, poor embryo quality and blastocyst formation have been major limitations for derivation of cloned ESCs (ntESCs). In this study, we have tried to overcome these problems by treating these cells with histone deacetylase inhibitors (HDACi) and aggregating porcine embryos. First, cloned embryos were treated with Scriptaid to confirm the effect of HDACi on cloned embryo quality. The Scriptaid-treated blastocysts showed significantly higher total cell numbers (29.50 +/- 2.10) than non-treated blastocysts (22.29 +/- 1.50, P < 0.05). Next, cloned embryo quality and blastocyst formation were analyzed in aggregates. Three zona-free, reconstructed, four-cell-stage SCNT embryos were injected into the empty zona of hatched parthenogenetic (PA) blastocysts. Blastocyst formation and total cell number of cloned blastocysts increased significantly for all aggregates (76.4% and 83.18 +/- 8.33) compared with non-aggregates (25.5% and 27.11 +/- 1.67, P < 0.05). Finally, aggregated blastocysts were cultured on a feeder layer to examine the efficiency of porcine ES-like cell derivation. Aggregated blastocysts showed a higher primary colony formation rate than non-aggregated cloned blastocysts (17.6 +/- 12.3% vs. 2.2 +/- 1.35%, respectively, P < 0.05). In addition, derived ES-like cells showed typical characters of ESCs. In conclusion, the aggregation of porcine SCNT embryos at the four-cell stage could be a useful technique for improving the development rate and quality of porcine-cloned blastocysts and the derivation efficiency of porcine ntESCs.
机译:来自大型动物物种的胚胎干细胞(ESC)的发展已成为使用通过体细胞核移植(SCNT)衍生的ESC进行治疗性克隆的重要模型。但是,不良的胚胎质量和胚泡形成一直是克隆ESC(ntESC)衍生的主要限制。在这项研究中,我们试图通过用组蛋白脱乙酰基酶抑制剂(HDACi)处理这些细胞并聚集猪胚来克服这些问题。首先,用Scriptaid处理克隆的胚胎,以确认HDACi对克隆的胚胎质量的影响。 Scriptaid处理的胚泡显示的总细胞数(29.50 +/- 2.10)明显高于未处理的胚泡(22.29 +/- 1.50,P <0.05)。接下来,对聚集体中克隆的胚胎质量和胚泡形成进行了分析。将三个无透明带,重建的,四细胞阶段的SCNT胚胎注入孵化的孤雌生殖(PA)胚泡的空透明带中。与非聚集体(25.5%和27.11 +/- 1.67,P <0.05)相比,所有聚集体的胚泡形成和克隆胚泡的总细胞数均显着增加(76.4%和83.18 +/- 8.33)。最后,将聚集的胚泡培养在饲养层上,以检查猪ES样细胞衍生的效率。聚集的胚泡比未聚集的克隆胚泡显示更高的原发菌落形成率(分别为17.6 +/- 12.3%和2.2 +/- 1.35%,P <0.05)。另外,衍生的ES样细胞显示出ESC的典型特征。总之,在四细胞阶段猪SCNT胚胎的聚集可能是提高猪克隆胚泡发育速度和质量以及猪ntESCs衍生效率的有用技术。

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