Role of estrogen receptor β in uterine stroma and epithelium: Insights from estrogen receptor β-/- mice

Osamu Wada-Hiraike, Haruko Hiraike, Hiroko Okinaga, Otabek Imamov, Rodrigo P.A. Barros, Andrea Morani, Yoko Omoto, Margaret Warner, Jan Åke Gustafsson

Research output: Contribution to journalArticle

91 Scopus citations

Abstract

In this study, we compared the uterine tissue of estrogen receptor (ER)β-/- mice and their WT littermates for differences in morphology, proliferation [the percentage of labeled cells 2 h after BrdUrd injection and EGF receptor (EGFR) expression], and differentiation (expression of progesterone receptor, E-cadherin, and cytokeratins). In ovariectomized mice, progesterone receptor expression in the uterine epithelium was similar in WT and ERβ-/- mice, but E-cadherin and cytokeratin 18 expression was lower in ERβ-/- mice. The percentage of cells in S phase was 1.5% in WT mice and 8% in ERβ-/- mice. Sixteen hours after injection of 17β-estradiol (E2), the number of BrdUrd-labeled cells increased 20-fold in WT mice and 80-fold in ERβ-/- mice. Although ERα was abundant in intact mice, after ovariectomy, ERα could not be detected in the luminal epithelium of either WT or ERβ-/- mice. In both untreated and E2-treated mice, ERα and ERβ were colocalized in the nuclei of many stromal and glandular epithelial cells. However, upon E2 + progesterone treatment, ERα and ERβ were not coexpressed in any cells. In WT mice, EGFR was located on the membranes and in the cytoplasm of luminal epithelium, but not in the stroma. In ERβ-/- mice, there was a marked expression of EGFR in the nuclei of epithelial and stromal cells. Upon E 2 treatment, EGFR on cell membranes was down-regulated in WT but not in ERβ-/- mice. These findings reveal an important role for ERβ in response to E2 and in the organization, growth, and differentiation of the uterine epithelium.

Original languageEnglish (US)
Pages (from-to)18350-18355
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume103
Issue number48
DOIs
StatePublished - Nov 28 2006

Keywords

  • Differentiation
  • Proliferation
  • Uterus

ASJC Scopus subject areas

  • Genetics
  • General

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