The roles of different protein kinases and of calmodulin in the effects of Ca2+ mobilization on 3-hydroxy-3-methylglutaryl-CoA reductase activity in isolated rat hepatocytes

Biochem J. 1991 Jan 15;273(Pt 2)(Pt 2):485-8. doi: 10.1042/bj2730485.

Abstract

The roles of protein kinase C, Ca2+/calmodulin-dependent protein kinase and AMP-activated protein kinase in the phosphorylation of 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase induced by Ca2(+)-mobilizing conditions in isolated hepatocytes were investigated. Only partial evidence for the involvement of AMP-activated kinase was found. Antagonism of calmodulin action prolonged the decrease in expressed/total activity ratio induced by vasopressin plus glucagon. Protease inhibitors active against Ca2(+)-dependent cytosolic proteases or lysosomal proteolysis did not attenuate the loss of total HMG-CoA reductase induced by glucagon plus vasopressin, but calmodulin antagonists largely prevented this effect.

MeSH terms

  • Adenosine Monophosphate / metabolism
  • Animals
  • Calcimycin / pharmacology
  • Calcium / pharmacology*
  • Calmodulin / pharmacology*
  • Cell Membrane / drug effects
  • Cell Membrane / enzymology
  • Enzyme Activation
  • Female
  • Hydroxymethylglutaryl CoA Reductases / metabolism*
  • Liver / enzymology*
  • Protease Inhibitors / pharmacology
  • Protein Kinase C / metabolism
  • Protein Kinases / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Substrate Specificity

Substances

  • Calmodulin
  • Protease Inhibitors
  • Calcimycin
  • Adenosine Monophosphate
  • Hydroxymethylglutaryl CoA Reductases
  • Protein Kinases
  • Protein Kinase C
  • Calcium