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Lysophosphatidic acid accelerates development of porcine embryos by activating formation of the blastocoel.

Authors :
Shin MY
Lee SE
Son YJ
Park YG
Jeong SG
Kim EY
Park SP
Source :
Molecular reproduction and development [Mol Reprod Dev] 2018 Jan; Vol. 85 (1), pp. 62-71. Date of Electronic Publication: 2018 Jan 15.
Publication Year :
2018

Abstract

Culture media modifications, including the addition of various factors, are important for the in vitro production of oocytes and embryos. In this study, we investigated the effects of lysophosphatidic acid (LPA) on porcine embryo development. Porcine parthenogenetic embryos were cultured with 0, 0.1, 1, and 10 μM LPA for 7 days, or cultured in basic medium until Day 4 and then treated with LPA from Days 4 to 7. No difference in the in vitro development of embryos cultured with LPA for 7 days was observed. Conversely, rates of blastocyst and over-expanded blastocyst formation were higher in the 0.1 and 1 µM LPA-treated versus the other groups of embryos treated from Days 4 to 7. Moreover, formation of early blastocysts occurred earlier and embryo size was larger in LPA-treated compared to control embryos. Expression of Connexin 43 and gap junction and cell adhesion-related genes (GJC1 and CDH1, respectively) was also higher in LPA-treated compared to control embryos. Despite no difference in the blastocyst total cell number between groups, the apoptotic index was lower in the LPA-treated group than in the control group; indeed, BCL2L1 (B-cell lymphoma 2-like protein 1) expression increased while BAK (Bcl-2 homologous antagonist killer) decreased in the LPA-treated group. Thus, addition of LPA to the medium from Days 4 to 7 of culture improves blastocyst formation and aids the development of preimplantation embryos.<br /> (© 2017 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1098-2795
Volume :
85
Issue :
1
Database :
MEDLINE
Journal :
Molecular reproduction and development
Publication Type :
Academic Journal
Accession number :
29226557
Full Text :
https://doi.org/10.1002/mrd.22938