Identification by hybridization histochemistry of human endometrial cells expressing mRNAs encoding a uterine beta-lactoglobulin homologue and insulin-like growth factor-binding protein-1

Mol Endocrinol. 1990 May;4(5):700-7. doi: 10.1210/mend-4-5-700.

Abstract

A beta-lactoglobulin homologue (beta LG/PP14) and insulin-like growth factor-binding protein-1 (IGFBP-1) are two major secretory proteins of the human endometrium. In the present study, we have shown that beta LG/PP14 mRNA is expressed in the endometrium in a cyclic manner, being hardly detectable in midcycle and most abundant during the late secretory phase. IGFBP-1 mRNA is also expressed in endometrium, but in amounts smaller than those encoding beta LG/PP14 and with maximal accumulation earlier in the secretory phase. The expression of these two mRNAs occurs in different cell types of the endometrium, as revealed by in situ hybridization techniques using single-stranded RNA probes. The glandular epithelial cells accumulate beta LG/PP14 mRNA during the late secretory phase of the cycle, whereas only the stromal cells of the late secretory endometrium express IGFBP-1 mRNA. In contrast to the endometrium, the two mRNAs are present at very low abundance in the fallopian tubes where they are expressed in the epithelial cells of the mucosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics*
  • Endometrium / metabolism*
  • Fallopian Tubes / metabolism
  • Female
  • Gene Expression
  • Histocytochemistry
  • Humans
  • Insulin-Like Growth Factor Binding Proteins
  • Insulin-Like Growth Factor I / metabolism
  • Lactoglobulins / genetics*
  • Nucleic Acid Hybridization
  • RNA Probes
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism

Substances

  • Carrier Proteins
  • Insulin-Like Growth Factor Binding Proteins
  • Lactoglobulins
  • RNA Probes
  • RNA, Messenger
  • Insulin-Like Growth Factor I