Concomitant expression of receptor subtype and isopeptide of endothelin by human adrenal gland

Biochem Biophys Res Commun. 1992 Feb 14;182(3):1115-21. doi: 10.1016/0006-291x(92)91847-j.

Abstract

We studied whether specific receptors for endothelin (ET) isopeptide exist in human aldosterone-producing adenoma and normal adrenal cortex, and whether ET isopeptides are produced by human adrenal gland. Competitive binding studies using [125I]ET-1 as a radioligand revealed the presence of a single class of high-affinity binding sites for ET-1 with the apparent KD of 70 +/- 31 pM and Bmax of 226 +/- 139 fmol/mg protein in adenoma membranes almost comparable to those in adjacent normal cortex. The apparent Ki for ET-2 and ET-3 were 89 +/- 33 pM and 82 +/- 16 pM, respectively. Northern blot analysis of poly(A)+ RNA of adenoma and adjacent normal cortex using cDNAs for ET receptor subtype (ETA, ETB) and ET isopeptide (ET-1, ET-3) as probes revealed that ETA and ETB receptors as well as ET isopeptides (preproET-1, preproET-3) are concomitantly expressed in both tissues. Our data demonstrate for the first time that ET receptor subtype (ETA and ETB) and ET isopeptide (ET-1 and ET-3) are concomitantly expressed by human adrenal cortex, suggesting the potential role of ETs as a local mediator in human adrenal gland.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / metabolism*
  • Adrenal Cortex / metabolism*
  • Adrenal Cortex Neoplasms / metabolism*
  • Adrenal Glands / metabolism*
  • Binding, Competitive
  • Blotting, Northern
  • Cloning, Molecular
  • Endothelins / biosynthesis
  • Endothelins / metabolism*
  • Humans
  • Isomerism
  • Kinetics
  • Poly A / genetics
  • Poly A / isolation & purification
  • RNA / genetics
  • RNA / isolation & purification
  • RNA, Messenger
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*
  • Receptors, Endothelin

Substances

  • Endothelins
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Endothelin
  • Poly A
  • RNA