cAMP-dependent down-regulation of endothelin-1 receptors on rat astrocytoma C6 cells

Neurosci Lett. 1991 Oct 14;131(2):175-8. doi: 10.1016/0304-3940(91)90607-u.

Abstract

The density of endothelin-1 (ET-1) receptors on rat astrocytoma C6 cells is down-regulated by activation of protein kinase C (PKC). We have investigated whether intracellular accumulation of cyclic adenosine monophosphate (cAMP) may also modulate surface ET-1 receptor number. The density of ET-1 receptors was measured by binding of [125I]ET-1 on rat astrocytoma C6 intact cells exposed to catecholamines, dibutyryl-cAMP or forskolin. Prolonged exposure of the cells to the beta-adrenergic agonists, isoproterenol or noradrenaline, results in a time- and dose-dependent decrease in cell surface ET-1 receptor number. This decrease proceeds slowly: maximal down-regulation is obtained by 6-7 h and sustained for up to 24 h in the presence of 10 microM isoproterenol. Since this down-regulation is mimicked by dibutyryl-cAMP (4 microM) and by forskolin (10 microM), we conclude that ET-1 receptors are susceptible to down-regulation through a cAMP-dependent pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytoma / metabolism*
  • Bucladesine / pharmacology
  • Colforsin / pharmacology
  • Cyclic AMP / physiology*
  • Down-Regulation / physiology*
  • Endothelins / physiology*
  • Iodine Radioisotopes
  • Isoproterenol / pharmacology
  • Norepinephrine / pharmacology
  • Protein Kinase C / metabolism
  • Rats
  • Receptors, Adrenergic, beta / drug effects
  • Receptors, Cell Surface / drug effects
  • Receptors, Cell Surface / physiology*
  • Receptors, Endothelin

Substances

  • Endothelins
  • Iodine Radioisotopes
  • Receptors, Adrenergic, beta
  • Receptors, Cell Surface
  • Receptors, Endothelin
  • Colforsin
  • Bucladesine
  • Cyclic AMP
  • Protein Kinase C
  • Isoproterenol
  • Norepinephrine