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Normal specification of the extraembryonic lineage after somatic nuclear transfer.

机译:体细胞核移植后胚外谱系的正常规格。

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To examine the establishment and maintenance of trophectoderm (TE) lineage in somatic cloned blastocysts, the expression of Cdx2, a key molecule for specification of TE fate, was immunohistochemically examined simultaneously with Oct4 expression. Cloned mouse embryos were made by nuclear transfer using cumulus cells, tail-tip fibroblasts, and embryonic stem cells. After 96 h of culture, the rates of Oct4-expressing blastocysts were as low as 50% and 60% for cumulus and fibroblast clones, respectively. However, regardless of Oct4 expression, the majority of those cloned blastocysts (> 90%) normally expressed Cdx2. Thus, even though somatic cloned embryos have reduced potential to produce the inner cell mass lineage, the TE lineage can be established and maintained.
机译:为了检查体细胞克隆胚泡中滋养外胚层(TE)谱系的建立和维持,同时通过免疫组织化学方法检测了Cdx2的表达,Cdx2是确定TE命运的关键分子,与Oct4表达同时进行了免疫组织化学检查。使用卵丘细胞,尾尖成纤维细胞和胚胎干细胞通过核移植制成克隆的小鼠胚胎。培养96小时后,积云和成纤维细胞克隆的Oct4表达胚泡率分别低至50%和60%。但是,无论Oct4表达如何,大多数克隆的胚泡(> 90%)都正常表达Cdx2。因此,即使体细胞克隆的胚胎产生内细胞群谱系的潜力降低,也可以建立和维持TE谱系。

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