Beta-adrenoceptor, vasoactive intestinal polypeptide (VIP) and neuropeptide tyrosine (NPY) receptors functionally coupled to adenylate cyclase in the human neuroblastoma SK-N-MC cell line

Neurosci Lett. 1987 Dec 16;83(1-2):161-6. doi: 10.1016/0304-3940(87)90234-5.

Abstract

Neurotransmitter receptor coupling to adenylate cyclase (AC) was studied in the cultured human neuroblastoma SK-N-MC cell line. Activation of beta-adrenoceptors with isoprenaline (ISO) or vasoactive intestinal polypeptide (VIP) receptors, increased AC activity in a dose-dependent manner. Preincubation with ISO and VIP induced a ligand specific, i.e. homologous type of desensitization of the respective receptor. Neuropeptide tyrosine (NPY) was able to inhibit ISO as well as VIP induced AC activity. The effect of NPY was totally abolished in cells pretreated with pertussis toxin to inactivate inhibitory G-proteins. Thus, SK-N-MC cells possess functionally coupled beta-adrenoceptors, VIP and NPY receptors, and may be used to study interactions between ligands and receptors which couple to the AC system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylyl Cyclases / metabolism*
  • Dose-Response Relationship, Drug
  • Humans
  • Isoproterenol / pharmacology
  • Receptors, Adrenergic, beta / metabolism*
  • Receptors, Gastrointestinal Hormone / metabolism*
  • Receptors, Neuropeptide Y
  • Receptors, Neurotransmitter / physiology
  • Receptors, Vasoactive Intestinal Peptide
  • Tumor Cells, Cultured
  • Vasoactive Intestinal Peptide / pharmacology

Substances

  • Receptors, Adrenergic, beta
  • Receptors, Gastrointestinal Hormone
  • Receptors, Neuropeptide Y
  • Receptors, Neurotransmitter
  • Receptors, Vasoactive Intestinal Peptide
  • Vasoactive Intestinal Peptide
  • Adenylyl Cyclases
  • Isoproterenol