Identification of insulin-like growth factor binding proteins in human oviduct

Fertil Steril. 1992 Feb;57(2):294-301.

Abstract

Objective: To determine if human oviduct expresses messenger ribonucleic acids (mRNAs) encoding insulin-like growth factor binding proteins (IGFBPs), if oviductal epithelium secretes IGFBPs into conditioned medium (CM), and if IGFBP secretion is regulated by steroid hormones.

Design: Northern blots of RNA, isolated from late proliferative phase human fimbria and oviductal isthmus, were probed with complementary deoxyribonucleic acids encoding IGFBP-1, IGFBP-2, IGFBP-3, and IGFBP-4. In addition, oviductal ampullary epithelial cells were cultured with and without estrogen and/or progesterone (P), and IGFBPs were examined in CM by Western ligand blot analysis and identified using specific antisera.

Setting: Tissue was obtained from hysterectomy specimens at Stanford University Hospital, a private teaching institution.

Patients, participants: Patients undergoing hysterectomy for benign disease.

Interventions: None.

Main outcome measures: Transcripts of IGFBP mRNA and IGFBPs secreted into CM were detected by autoradiography of Northern and Western ligand blots, respectively.

Results: Messenger RNA transcripts encoding IGFBP-2, -3, and -4 were detected, whereas IGFBP-1 mRNA was barely detectable in oviductal tissue. In CM, IGFBP-2 and IGFBP-3 were detected, as was a unique 24-kd IGFBP, although IGFBP-1 was not observed. Estrogen and/or P did not regulate the secretion of these IGFBPs by cultured oviductal epithelium.

Conclusions: Human oviduct expresses mRNAs encoding IGFBP-2, IGFBP-3, and IGFBP-4, and in vitro oviductal epithelium secretes IGFBP-2, IGFBP-3, and a unique binding protein of 24 kd, which may be the recently identified IGFBP-4.

Publication types

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

MeSH terms

  • Animals
  • Autoradiography
  • Blotting, Northern
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cells, Cultured
  • Culture Media
  • Epithelial Cells
  • Epithelium / metabolism
  • Fallopian Tubes / cytology
  • Fallopian Tubes / metabolism*
  • Female
  • Humans
  • Insulin-Like Growth Factor Binding Proteins
  • Precipitin Tests
  • Protein Biosynthesis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Somatomedins / metabolism

Substances

  • Carrier Proteins
  • Culture Media
  • Insulin-Like Growth Factor Binding Proteins
  • RNA, Messenger
  • Somatomedins