ATP induces c-fos expression in C6 glioma cells by activation of P(2Y) receptors

J Surg Res. 2000 Nov;94(1):49-55. doi: 10.1006/jsre.2000.5984.

Abstract

Background: Extracellular ATP functions in the enteric nervous system as a neurotransmitter, and recent evidence suggests ATP may regulate development through effects on cellular proliferation.

Methods: The action of ATP at purinoceptors and the role of second messenger pathways in c-fos mRNA expression in C6 glioma cells were investigated using the techniques of Northern and Western blotting.

Results: Treatment of C6 cells with ATP caused a time- and dose-dependent increase in c-fos expression. The rank order of agonist potency was ATP = ADP > gammasATP > alphabetaATP > betagammaATP > AMP = UTP. The ATP-induced c-fos increment was inhibited by three P(2Y) receptor antagonists-suramin, reactive blue, and DIDS-by 99+/-3, 89+/-7, and 61+/-14%, respectively. The ATP-stimulated c-fos expression was attenuated by phospholipase C inhibitor (U73122), protein kinase C (PKC) down-regulation (4alpha-phorbol 12-myristate 13-acetate and chelerythrine), mitogen-activated protein (MAP) kinase inhibition (apigenin), an inhibitor of MAP kinase kinase (PD98059), down-regulation of adenylate cyclase (SQ22536), and inhibition of type II protein kinase A (8-(4-chlorophenylthio)adenosine-3',5'-cyclic monophosphorothioate), but was not affected by inhibition of type I protein kinase A (8-bromoadenosine-3',5'-cyclic monophosphorothioate) and inhibitors of calmodulin kinase (KN93 and KN62). Phosphorylated MAP kinase was increased in cells exposed to ATP. This effect was suppressed by chelerythrine.

Conclusions: These studies demonstrate that ATP-induced c-fos mRNA expression is under multifactorial regulation.

MeSH terms

  • Adenosine Triphosphate / pharmacology*
  • Animals
  • Cyclic AMP / physiology
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Genes, fos*
  • Glioma / genetics*
  • MAP Kinase Signaling System
  • Protein Kinase C / physiology
  • RNA, Messenger / analysis
  • Rats
  • Receptors, Purinergic P2 / physiology*
  • Tumor Cells, Cultured
  • Type C Phospholipases / physiology

Substances

  • RNA, Messenger
  • Receptors, Purinergic P2
  • Adenosine Triphosphate
  • Cyclic AMP
  • Protein Kinase C
  • Type C Phospholipases