P-47: Effect of Blastocoelic Fluid Reduction on Quality and Expression of Developmentally Important Genes in Mouse Blastocysts

Authors

  • F Mahdavinezhad Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
  • GH Zandi Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
  • M Dashtizad Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
  • M Shamsara Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
  • P Fathalizade Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
  • P Kazemi Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
Abstract:

Background Recent researches reveal that manual puncturing of the trophectoderm of blastocyst before vitrification, increase the quality of embryo. However, in any of these studies, the importance of blastocoelic fluid and its impact on the formation of three cell lines is not mentioned. Therefore, in the present study, the effect of blastocoelic fluid reduction before vitrification on survival and hatching rate, expression of lineage specific genes (Oct4, Nanog, Cdx2, Eomes and Gata6), and apoptosis related gene (P53) in mouse blastocyst was studied. MaterialsAndMethods For this purpose, two sources of In vitro and In vivo produced mouse embryos were used and randomly divided in to three groups. 1. Vitrified/warmed blastocysts, 2. Vitrified/warmed blastocysts after artificial collapse (AC) and 3. Fresh blastocysts as control group. The survival and hatching rates of embryos were evaluated. After total RNA extraction of three groups, Real time PCR was accomplished. Results The survival rate of treatments was similar to the control group. The hatching rate of AC-vitrified/warmed blastocysts was significantly higher than that of non-AC group. The expression results of two sources were approximately similar. There was no significant change in expression of pluripotency genes (Oct4, Nanog) between vitrified/warmed and AC-vitrified/warmed blastocyst. The expression of Cdx2, Eomes, Gata6, and P53 in AC-vitrified/warmed was reduced in compared with vitrified/warmed blastocyst (P

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Journal title

volume 9  issue 2

pages  63- 63

publication date 2015-09-01

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