cAMP-dependent positive control of cyclin A2 expression during G1/S transition in primary hepatocytes

Biochem Biophys Res Commun. 1999 Jul 22;261(1):118-22. doi: 10.1006/bbrc.1999.0575.

Abstract

cAMP positively and negatively regulates hepatocyte proliferation but its molecular targets are still unknown. Cyclin A2 is a major regulator of the cell cycle progression and its synthesis is required for progression to S phase. We have investigated whether cyclin A2 and cyclin A2-associated kinase might be one of the targets for the cAMP transduction pathway during progression of hepatocytes through G1 and G1/S. We show that stimulation of primary cultured hepatocytes by glucagon differentially modulated the expression of G1/S cyclins. Glucagon indeed upregulated cyclin A2 and cyclin A2-associated kinase while cyclin E-associated kinase was unmodified. In conclusion, our study identifies cyclin A2 as an important effector of the cAMP transduction network during hepatocyte proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Division / drug effects
  • Cells, Cultured
  • Cyclic AMP / metabolism*
  • Cyclin A / metabolism*
  • Cyclin A2
  • Cyclin-Dependent Kinases / metabolism
  • Cyclins / metabolism
  • DNA / biosynthesis
  • G1 Phase* / drug effects
  • Glucagon / pharmacology
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Rats
  • Rats, Wistar
  • S Phase* / drug effects
  • Signal Transduction / drug effects
  • Time Factors
  • Up-Regulation / drug effects

Substances

  • Ccna2 protein, rat
  • Cyclin A
  • Cyclin A2
  • Cyclins
  • DNA
  • Glucagon
  • Cyclic AMP
  • Cyclin-Dependent Kinases