Developmental changes in cyclic AMP-stimulated stellation of cultured rat cortical astrocytes

Jpn J Pharmacol. 1997 Dec;75(4):433-8. doi: 10.1254/jjp.75.433.

Abstract

When cultured astrocytes are treated with agents that elevate intracellular cyclic AMP, they become process-bearing stellate cells. In the present study, we investigated possible developmental changes of astrocyte stellation induced by beta-adrenoceptor stimulaton. Cultured astrocytes were prepared from the cerebral cortices of embryonic day 18 (E18) and postnatal day 2 (P2) rats. Treatment with the beta-adrenoceptor agonist isoproterenol induced stellation in P2 astrocytes more potently and rapidly than in E18 astrocytes. Isoproterenol-stimulated increase in cellular cyclic AMP levels was very similar in E18 and P2 astrocytes. The membrane-permeable cyclic AMP analog dibutyryl cyclic AMP induced stellation in P2 astrocytes more potently and rapidly than in E18 astrocytes. Stellation induced by the protein kinase C activator phorbol ester was not different between E18 and P2 astrocytes. These results suggest that beta-adrenoceptor-mediated astrocyte stellation increases during development and that this change is attributed to the development of mechanisms downstream from cyclic AMP production.

Publication types

  • Comparative Study

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Animals, Newborn
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Bucladesine
  • Cell Aggregation / drug effects*
  • Cells, Cultured
  • Cerebral Cortex / drug effects*
  • Cerebral Cortex / embryology
  • Cerebral Cortex / growth & development
  • Cyclic AMP / metabolism*
  • Glial Fibrillary Acidic Protein / biosynthesis
  • Isoproterenol / pharmacology*
  • Protein Kinase C
  • Rats
  • Rats, Wistar
  • Tetradecanoylphorbol Acetate

Substances

  • Adrenergic beta-Agonists
  • Glial Fibrillary Acidic Protein
  • Bucladesine
  • Cyclic AMP
  • Protein Kinase C
  • Isoproterenol
  • Tetradecanoylphorbol Acetate