Preimplantation embryo-secreted factors modulate maternal gene expression in rat uterus

Cell Tissue Res. 2016 May;364(2):453-63. doi: 10.1007/s00441-015-2336-z. Epub 2015 Dec 19.

Abstract

In mammalian reproduction, embryo implantation into the uterus is spatiotemporally regulated by a complex process triggered by a number of factors. Although previous studies have suggested that uterine receptivity is mediated by blastocyst-derived factors, specific functions of embryos remain to be defined during preimplantation. Therefore, the present study was conducted to identify the maternal genes regulated by embryo-secreted factors in the rat uterus. RNA-sequencing (RNA-seq) data revealed that 10 genes are up-regulated in the delayed implantation uterus compared with the pseudopregnancy uterus. The RNA-seq results were further verified by real-time quantitative polymerase chain reaction. Sulf1 expression is significantly (P < 0.05) induced in the delayed implantation uterus, although Areg, Calca, Fxyd4 and Lamc3 show a definite but non-statistically significant increase in their expression levels. During early pregnancy, the levels of Areg, Calca, Fxyd4, Lamc3 and Sulf1 expression at 3.5 days post coitus (dpc) are significantly (P < 0.05) higher than those at 1.5 dpc. Treatment with embryo-conditioned media revealed that Lamc3 and Sulf1 are up-regulated compared with the other genes studied. Thus, embryo-derived factors regulate maternal gene expression, with Lamc3 and Sulf1 possibly being suitable markers for a response study of embryo-secreted factors to improve our understanding of embryo-maternal communication.

Keywords: Embryo-secreted factors; Lamc3; RNA-sequencing; Sulf1; Uterus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst / metabolism*
  • Embryo Culture Techniques
  • Embryo Implantation / genetics*
  • Embryo Implantation / physiology
  • Embryo, Mammalian / metabolism*
  • Female
  • Gene Expression
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental*
  • Rats
  • Rats, Wistar
  • Uterus / metabolism*