2-Aminopurine inhibits RNA and protein synthesis and reduces catecholamine desensitization in C6-2B rat glioma cells

FEBS Lett. 1992 Jan 13;296(1):112-6. doi: 10.1016/0014-5793(92)80415-d.

Abstract

We previously proposed that intracellular cyclic AMP accumulation induces a putative, rapidly turning over protein inhibitory to further hormone activation of adenylate cyclase. In the present study, 2-aminopurine, which has been reported to selectively block c-fos gene expression, was used to test the hypothesis that c-fos protein might be involved in the desensitization to catecholamines was observed in 2-aminopurine-treated C6-2B rat glioma cells. However, we found 2-aminopurine to inhibit, in a concentration-dependent manner, total cellular RNA and protein synthesis in C6-2B, HeLa, Swiss 3T3 and BALB/c cells. mRNA synthesis was also markedly reduced in 2-aminopurine-treated cells. These unexpected findings, while supporting our hypothesis of a protein synthesis-sensitive step in the development of refractoriness, raise concern about the specificity of action of 2-aminopurine to inhibit c-fos induction and thus any cellular process, including desensitization, which might be regulated by c-fos gene expression.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 2-Aminopurine / pharmacology*
  • 3T3 Cells / drug effects
  • Animals
  • Bucladesine / pharmacology
  • Catecholamines / metabolism*
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Drug Interactions
  • Gene Expression / drug effects
  • Glioma
  • HeLa Cells / drug effects
  • Humans
  • Isoproterenol / pharmacology
  • Methionine / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Protein Biosynthesis
  • Protein Synthesis Inhibitors / pharmacology*
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-fos / metabolism
  • RNA / biosynthesis*
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Rats
  • Tumor Cells, Cultured / drug effects
  • Uridine / metabolism

Substances

  • Catecholamines
  • Protein Synthesis Inhibitors
  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger
  • Colforsin
  • 2-Aminopurine
  • RNA
  • Bucladesine
  • Methionine
  • Cyclic AMP
  • Isoproterenol
  • Uridine