Analysis of heart and neural crest derivatives-expressed protein 2 (HAND2)-progesterone interactions in peri-implantation endometrium†

Biol Reprod. 2020 Apr 24;102(5):1111-1121. doi: 10.1093/biolre/ioaa013.

Abstract

Implantation is restricted to a narrow window when the local endometrial microenvironment is supportive of the invading embryo. The ovarian steroid hormones estrogen (E) and progesterone (P) are principal regulators of uterine receptivity. Suppression of E-dependent proliferation of luminal epithelium (LE) by P is mandatory for embryo implantation. Here, we report that the balance of E receptor α (ERα) and P receptors (PR) activity controls HAND2 expression, a key transcription factor that determines the fate of the implanting embryo and thereby pregnancy outcome. As a model, we used wild-type mice as well as mice in which either both PR isoforms or the A-isoform was genetically ablated (PRKO and PRAKO, respectively). Detailed spatiotemporal analyses of PR, HAND2, and ERα expression at implantation site demonstrated co-expression of HAND2 and PR but not ERα. Furthermore, in hormonally treated ovariectomized WT, PRAKO and PRKO mice, E suppresses endometrial HAND2 expression. Adding P together with E partially rescues HAND2 expression in WT, but not PRAKO and PRKO animals. Therefore, infertility in PRAKO mice is at least in part associated with the loss of PR-A-regulated HAND2 expression.

Keywords: HAND2; endometrium; estradiol/estradiol receptor; implantation; progesterone/progesterone receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Embryo Implantation
  • Endometrium / drug effects*
  • Estrogen Receptor alpha
  • Estrogens / pharmacology
  • Female
  • Gene Expression Regulation / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Ovariectomy
  • Pregnancy
  • Progesterone / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Progesterone / genetics
  • Receptors, Progesterone / metabolism*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Estrogen Receptor alpha
  • Estrogens
  • Hand2 protein, mouse
  • RNA, Messenger
  • Receptors, Progesterone
  • Progesterone