HB-EGF regulates Prss56 expression during mouse decidualization via EGFR/ERK/EGR2 signaling pathway

J Endocrinol. 2017 Sep;234(3):247-254. doi: 10.1530/JOE-16-0636. Epub 2017 Jun 13.

Abstract

Embryo implantation and decidualization are key steps for successful reproduction. Although numerous factors have been identified to be involved in embryo implantation and decidualization, the mechanisms underlying these processes are still unclear. Based on our preliminary data, Prss56, a trypsin-like serine protease, is strongly expressed at implantation site in mouse uterus. However, the expression, regulation and function of Prss56 during early pregnancy are still unknown. In mouse uterus, Prss56 is strongly expressed in the subluminal stromal cells at implantation site on day 5 of pregnancy compared to inter-implantation site. Under delayed implantation, Prss56 expression is undetected. After delayed implantation is activated by estrogen, Prss56 is obviously induced at implantation site. Under artificial decidualization, Prss56 signal is seen at the primary decidual zone at the initial stage of artificial decidualization. When stromal cells are induced for in vitro decidualization, Prss56 expression is significantly elevated. Dtprp expression under in vitro decidualization is suppressed by Prss56 siRNA. In cultured stromal cells, HB-EGF markedly stimulates Prss56 expression through EGFR/ERK pathway. Based on promoter analysis, we also showed that Egr2 is involved in Prss56 regulation by HB-EGF. Collectively, Prss56 expression at implantation site is modulated by HB-EGF/EGFR/ERK signaling pathway and involved in mouse decidualization.

Keywords: Prss56; decidualization; endometrium; uterus.

MeSH terms

  • Animals
  • Early Growth Response Protein 2 / genetics
  • Early Growth Response Protein 2 / metabolism*
  • Embryo Implantation
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Estrogens / metabolism
  • Female
  • Heparin-binding EGF-like Growth Factor / genetics
  • Heparin-binding EGF-like Growth Factor / metabolism*
  • MAP Kinase Signaling System
  • Mice
  • Pregnancy
  • Serine Proteases / genetics
  • Serine Proteases / metabolism*
  • Signal Transduction
  • Uterus / metabolism

Substances

  • Early Growth Response Protein 2
  • Egr2 protein, mouse
  • Estrogens
  • Heparin-binding EGF-like Growth Factor
  • EGFR protein, mouse
  • ErbB Receptors
  • Prss56 protein, mouse
  • Serine Proteases