Cocaine- and amphetamine-regulated transcript (CART) peptide activates the extracellular signal-regulated kinase (ERK) pathway in AtT20 cells via putative G-protein coupled receptors

Neurosci Lett. 2005 Aug;384(1-2):198-202. doi: 10.1016/j.neulet.2005.04.072.

Abstract

CART peptides are important neurotransmitters, but little is known about their receptors or signaling pathways in cells. In this study we describe the effects of CART 55-102 on the stimulation of extracellular signal-related kinase (ERK) in a pituitary-derived cell line. CART 55-102 treatment resulted in markedly enhanced ERK phosphorylation in AtT20 and GH3 cells, but had no significant effect on ERK phosphorylation levels in a variety of other cell types that were examined. The peptide activated ERK1 and 2 in AtT20 cells in a dose- and time-dependent manner, but an inactive peptide, CART 1-27, had no effect. U0126, an inhibitor of the MEK kinases, blocked the CART-stimulated activation of ERKs. ERK activation was also attenuated by pertussis toxin pre-treatment, but not by genistein, suggesting a Gi/o-dependent mechanism. Overall, these data strongly support the existence of a specific receptor for CART peptide that is a G-protein coupled receptor utilizing a Gi/o mechanism involving MEK1 and 2.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Analysis of Variance
  • Animals
  • Blotting, Western / methods
  • Butadienes / pharmacology
  • Cell Line
  • Dose-Response Relationship, Drug
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Genistein / pharmacology
  • Mice
  • Nerve Tissue Proteins / pharmacology*
  • Nitriles / pharmacology
  • Peptide Fragments / pharmacology
  • Pertussis Toxin / pharmacology
  • Phosphorylation / drug effects
  • Pituitary Gland / cytology
  • Receptors, G-Protein-Coupled / physiology*
  • Signal Transduction / drug effects*
  • Time Factors

Substances

  • Butadienes
  • Enzyme Inhibitors
  • Nerve Tissue Proteins
  • Nitriles
  • Peptide Fragments
  • Receptors, G-Protein-Coupled
  • U 0126
  • cocaine- and amphetamine-regulated transcript protein
  • Genistein
  • Pertussis Toxin
  • Extracellular Signal-Regulated MAP Kinases