A luciferase-engineered cell line for study of cAMP regulation in endothelial cells

Am J Physiol. 1998 Jul;275(1):C75-81. doi: 10.1152/ajpcell.1998.275.1.C75.

Abstract

cAREL is a cAMP-responsive endothelial cell line carrying a luciferase reporter gene introduced by stable transfection of a luciferase enhancer trap into rabbit aortic endothelial cells. Luciferase gene expression in cAREL was stimulated 233-fold by 8-BrcAMP. Treatment with the beta-adrenoceptor agonist isoproterenol induced a 7.0-fold increase in luciferase expression, which was partially blocked by either beta1- or beta2-adrenoceptor antagonists and totally blocked by propranolol and by a combination of beta1- plus beta2-adrenoceptor antagonists. Receptor stimulation was mimicked by cholera toxin, forskolin, 8-BrcAMP, and isobutylmethylxanthine but not by 8BrcGMP, dexamethasone, or phorbol 12-myristate 13-acetate. Stimulation by isoproterenol was completely blocked by H-89, a protein kinase A inhibitor. cAREL was also stimulated by A-23187, and this effect was abrogated by EGTA and H-89. cAREL is the first cAMP-sensitive endothelial cell line described, and it can be useful as a positive control, as a model for cAMP regulation, as a background to genetic introduction of receptors, as an indicator of intracellular pathway activation, and as a tool to investigate cAMP effects on other signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • 8-Bromo Cyclic Adenosine Monophosphate / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Aorta
  • Calcimycin / pharmacology
  • Cell Line
  • Cholera Toxin / pharmacology
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Endothelium, Vascular / cytology*
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism
  • Enhancer Elements, Genetic
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation / drug effects*
  • Genes, Reporter
  • Isoproterenol / pharmacology
  • Isoquinolines / pharmacology
  • Kinetics
  • Luciferases / biosynthesis*
  • Rabbits
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Sulfonamides*
  • Transfection / methods*

Substances

  • Adrenergic beta-Antagonists
  • Enzyme Inhibitors
  • Isoquinolines
  • Sulfonamides
  • Colforsin
  • 8-Bromo Cyclic Adenosine Monophosphate
  • Calcimycin
  • Cholera Toxin
  • Cyclic AMP
  • Luciferases
  • Cyclic AMP-Dependent Protein Kinases
  • Isoproterenol
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide
  • 1-Methyl-3-isobutylxanthine