Differential expression and regulation of angiopoietin-3 in mouse uterus during preimplantation period

J Exp Zool B Mol Dev Evol. 2012 Jun;318(4):316-24. doi: 10.1002/jez.b.22449.

Abstract

Angiogenesis is necessary for successful implantation and decidualization. This study was to investigate the differential expression of angiopoietin-3 (Ang-3) in mouse uterus during early pregnancy and its regulation by steroid hormones using in situ hybridization and reverse transcription polymerase chain reaction (RT-PCR). There was no detectable Ang-3 mRNA signal on days 1-5 of pregnancy by in situ hybridization. On day 6 of pregnancy, a low level of Ang-3 mRNA signal was seen in the primary decidua. Ang-3 mRNA expression gradually increased on days 7 and 8 of pregnancy along with the development of decidua, and its expression scope was also expanded. The RT-PCR result indicated that Ang-3 mRNA expression was low on days 1-4 of pregnancy. On day 5, as embryo implanted, Ang-3 mRNA was highly expressed in mouse uterus, and the expression gradually increased on days 6-8 of pregnancy, with peak level on day 8 of pregnancy. Similarly, Ang-3 mRNA was also strongly expressed in decidualized cells under artificial decidualization. Compared with the delayed uterus, a high level of Ang-3 mRNA expression was detected in activated implantation uterus by RT-PCR. In the ovariectomized mouse uterus, Ang-3 mRNA expression increased and reached the highest level at 12 hr after injection of estrogen, progesterone, and estrogen plus progesterone, respectively. These results suggest that Ang-3 may play an important role during the process of mouse decidualization. Both estrogen and progesterone can induce the expression of Ang-3 in ovariectomized mouse uterus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiopoietins / metabolism*
  • Animals
  • Embryo Implantation / physiology
  • Estradiol / analogs & derivatives
  • Estradiol / pharmacology
  • Estrogen Antagonists / pharmacology
  • Estrogens / pharmacology
  • Female
  • Fulvestrant
  • Gene Expression Regulation, Developmental / physiology*
  • In Situ Hybridization
  • Mice
  • Mifepristone / pharmacology
  • Neovascularization, Physiologic / physiology*
  • Pregnancy
  • Progesterone / antagonists & inhibitors
  • Progesterone / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Uterus / metabolism*

Substances

  • Angiopoietins
  • Estrogen Antagonists
  • Estrogens
  • angiopoietin 4
  • Fulvestrant
  • Mifepristone
  • Progesterone
  • Estradiol