Literature DB >> 22383776

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

G Giritharan1, L Delle Piane, A Donjacour, F J Esteban, J A Horcajadas, E Maltepe, P Rinaudo.   

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.

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Year:  2012        PMID: 22383776      PMCID: PMC3343151          DOI: 10.1177/1933719111428522

Source DB:  PubMed          Journal:  Reprod Sci        ISSN: 1933-7191            Impact factor:   3.060


  42 in total

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Authors:  J Rossant; J C Cross
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4.  Combining mouse congenic strains and microarray gene expression analyses to study a complex trait: the NOD model of type 1 diabetes.

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5.  Low and very low birth weight in infants conceived with use of assisted reproductive technology.

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7.  Eomesodermin is required for mouse trophoblast development and mesoderm formation.

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  18 in total

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2.  The WNT signaling antagonist Dickkopf-1 directs lineage commitment and promotes survival of the preimplantation embryo.

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7.  Comparative intrauterine development and placental function of ART concepti: implications for human reproductive medicine and animal breeding.

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9.  In Vitro Fertilisation of Mouse Oocytes in L-Proline and L-Pipecolic Acid Improves Subsequent Development.

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Journal:  BMC Dev Biol       Date:  2012-11-06       Impact factor: 1.978

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