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在体外培养的小鼠胚胎中降低了内细胞团和滋养外胚层之间的差异基因表达。

In vitro culture of mouse embryos reduces differential gene expression between inner cell mass and trophectoderm.

机构信息

Department of Obstetric and Gynecology, University of California, San Francisco, San Francisco, CA 94115, USA.

出版信息

Reprod Sci. 2012 Mar;19(3):243-52. doi: 10.1177/1933719111428522.

Abstract

Differences in gene expression and imprinting have been reported, comparing in vivo versus in vitro generated preimplantation embryos. Furthermore, mouse studies have shown that placenta development is altered following in vitro culture. However, the molecular mechanisms underlying these findings are unknown. We therefore isolated trophectoderm (TE) and inner cell mass (ICM) cells from in vivo and in vitro fertilization (IVF) embryos and evaluated their transcriptome using microarrays. We found that the transcriptomes of in vitro produced ICM and TE cells showed remarkably few differences compared to ICM and TE cells of in vivo generated embryos. In vitro fertilization embryos showed a reduced number of TE cells compared to in vivo embryos. In addition, TE of IVF embryos showed significant downregulation of solute transporter genes and of genes involved in placenta formation (Eomesodermin, Socs3) or implantation (Hbegf). In summary, IVF and embryo culture significantly affects the transcriptome of ICM and TE cells.

摘要

已经有报道称,与体内生成的胚胎相比,体外生成的胚胎在基因表达和印迹上存在差异。此外,老鼠研究表明,胎盘发育在体外培养后发生改变。然而,这些发现的分子机制尚不清楚。因此,我们从体内和体外受精(IVF)胚胎中分离滋养外胚层(TE)和内细胞团(ICM)细胞,并使用微阵列评估它们的转录组。我们发现,与体内生成的胚胎的 ICM 和 TE 细胞相比,体外生成的 ICM 和 TE 细胞的转录组差异很小。与体内胚胎相比,体外受精胚胎的 TE 细胞数量减少。此外,IVF 胚胎的 TE 显示溶质转运基因以及参与胎盘形成(Eomesodermin、SocS3)或植入(Hbegf)的基因显著下调。总之,IVF 和胚胎培养显著影响 ICM 和 TE 细胞的转录组。

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