Epidermal growth factor and sex steroids dynamically regulate a marker of endometrial receptivity in Ishikawa cells

J Clin Endocrinol Metab. 1997 Jul;82(7):2192-7. doi: 10.1210/jcem.82.7.4102.

Abstract

The factors regulating human endometrial receptivity remain poorly understood. The alpha v beta 3 integrin cell adhesion molecule appears to be regulated in the human endometrium, appearing on postovulatory days 5-6, corresponding to the time of initial embryo attachment. This integrin has been extensively studied as a potential marker of endometrial receptivity and is aberrantly expressed in the endometrial epithelium of some infertile women. Ishikawa cells are a well differentiated endometrial adenocarcinoma cell line that maintain functional estrogen and progesterone receptors and are a useful model to study steroid-mediated events in human endometrial epithelium. This cell line expresses most of the normal endometrial epithelial integrins, including the alpha v beta 3 vitronectin receptor. The regulation of this integrin was studied with fluorescence immunocytochemistry, flow cytometry, and Northern blot analysis. Estrogen with or without progesterone treatment down-regulates alpha v beta 3 in this cell line. Several growth factors, including epidermal growth factor and the closely related transforming growth factor-alpha significantly increase the expression of this integrin. We conclude that endometrial differentiation is influenced by both steroid hormones and growth factors. The alpha v beta 3 integrin appears to be an excellent marker to study the molecular events leading to the establishment of uterine receptivity and successful implantation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma / metabolism*
  • Biomarkers / analysis
  • Blotting, Northern
  • Cytokines / pharmacology
  • Dose-Response Relationship, Drug
  • Endometrial Neoplasms / metabolism*
  • Epidermal Growth Factor / pharmacology*
  • Estrogens / pharmacology*
  • Female
  • Flow Cytometry
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Progesterone / pharmacology*
  • Receptors, Vitronectin / metabolism*
  • Tumor Cells, Cultured

Substances

  • Biomarkers
  • Cytokines
  • Estrogens
  • Receptors, Vitronectin
  • Progesterone
  • Epidermal Growth Factor