Expression of vigilin in the uterus of ovariectomized steroid-treated rats and during the estrous cycle

Ann Anat. 1996 Aug;178(4):337-44. doi: 10.1016/S0940-9602(96)80089-6.

Abstract

The expression of vigilin in the uterus of rats was investigated by immunoblotting and immunohistochemistry and compared to the ultrastructural features of the endometrial cells. Vigilin could not be detected in the uteri of ovariectomized rats. Administration of estrogen, alone or in combination with progesterone, significantly stimulated the expression of vigilin, mainly in the luminal and glandular epithelial cells. Ultrastructurally, these cells show the morphological features of an increased protein synthesis. Untreated mature rats demonstrate a cyclic pattern of vigilin expression with high levels during the estrogen-dominated proestrus and early estrus stages and low levels at metestrus. The down-regulation of vigilin starts with the occurrence of apoptosis and autophagocytosis in the epithelium, but precedes the vanishing of the secretory granules. At diestrus the vigilin expression is intermediate and the vigilin staining of the epithelial cells is reduced. However, the endometrial fibroblasts show a faint staining. Morphologically, these fibroblasts are characterized by large euchromatic nuclei and dilated cisternae of the rough endoplasmic reticulum. The results suggest that in the uterus of rats the expression of vigilin is stimulated by estrogen. Under the experimental conditions chosen no influence of progesterone on vigilin expression was detected.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins*
  • Epithelium / drug effects
  • Epithelium / metabolism
  • Epithelium / ultrastructure
  • Estrone / pharmacology*
  • Estrus / physiology*
  • Female
  • Immunohistochemistry
  • Microscopy, Electron
  • Ovariectomy
  • Progesterone / pharmacology*
  • Protein Biosynthesis*
  • Proteins / analysis
  • RNA-Binding Proteins*
  • Rats
  • Rats, Wistar
  • Sexual Maturation
  • Uterus / drug effects
  • Uterus / metabolism*
  • Uterus / ultrastructure

Substances

  • Carrier Proteins
  • Proteins
  • RNA-Binding Proteins
  • high density lipoprotein binding protein
  • Estrone
  • Progesterone