Regulation of the expression of the phosphoenolpyruvate carboxykinase gene in cultured rat hepatocytes by glucagon and insulin

• Published in: European journal of biochemistry Vol. 178; no. 2; pp. 373 - 379
• Main Authors: CHRIST, Bruno, NATH, Annegret, BASTIAN, Helge, JUNGERMANN, Kurt
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 15.12.1988; Blackwell
• Subjects: Animals; Biological and medical sciences; Cells, Cultured; Enzyme Induction - drug effects; Fundamental and applied biological sciences. Psychology; Gene expression; Gene Expression Regulation - drug effects; Glucagon - pharmacology; Glucagon - physiology; Insulin - pharmacology; Liver - enzymology; Male; Molecular and cellular biology; Molecular genetics; Phosphoenolpyruvate Carboxykinase (GTP) - biosynthesis; Phosphoenolpyruvate Carboxykinase (GTP) - genetics; Rats; Rats, Inbred Strains; RNA, Messenger - metabolism; Transcription, Genetic; Cell culture; Glucagon; Rat; Rodentia; Gene expression; Insulin; Protein hormone; Vertebrata; Regulation(control); Mammalia; Hepatocyte; Hormonal regulation; Phosphoenolpyruvate carboxykinase (ATP)
• ISSN: 0014-2956; 1432-1033
• DOI: 10.1111/j.1432-1033.1988.tb14460.x

The induction of phosphoenolpyruvate carboxykinase (PEPCK) by glucagon was studied in primary rat hepatocyte cultures by determining the time course of the sequential events, increases in the enzyme's mRNA abundance, synthesis rate, amount and activity, and by investigating the antagonistic action of insulin on the induction by glucagon. 1 The mRNA of PEPCK was induced maximally 2–3 h after addition of 10 nM glucagon, as detected by Northern‐blot analysis after hybridization with a biotinylated antisense RNA of PEPCK. 2 The synthesis rate of PEPCK increased maximally 2–3 h after application of glucagon as revealed by pansorbin‐linked immunoprecipitation of [35S]methionine‐labelled PEPCK. 3 The enzyme amount and activity was maximally induced 4 h after glucagon application. 4 The mRNA of PEPCK was half‐maximally induced by 0.1 nM and maximally by 1 nM and 10 nM glucagon. The half‐maximal induction by 0.1 nM glucagon was antagonized almost totally, and the maximal induction by 1 nM glucagon partially, while the maximal induction by 10 nM glucagon remained unaffected by 10 nM insulin. The results show that in cultured rat hepatocytes physiological concentrations of glucagon stimulated the induction of PEPCK by an increase in mRNA, that the glucagon‐dependent increase in mRNA and enzyme‐synthesis rate occurred in parallel and preceded the increase of enzyme amount and activity by 1–1.5 h, and that physiological levels of insulin antagonized the induction by glucagon in the physiological concentration range with glucagon being the dominant hormone.