Abstract
It is now well established that the transcription of several genes belonging to the glycolytic and lipogenic pathway is stimulated in the presence of a high glucose concentration in adipocytes and hepatocytes. We have previously proposed that glucose 6-phosphate could be the signal metabolite that transduces the glucose effect. This proposal has recently been challenged and both an intermediate of the pentose phosphate pathway, xylulose 5-phosphate, and metabolites of the later part of glycolysis (3-phosphoglycerate and phosphoenolpyruvate) have been proposed. To discriminate between these possibilities, we have measured concomitantly, in primary cultures of adult rat hepatocytes, the expression of the fatty acid synthase (FAS) and S14 genes and the concentration of glucose metabolites. We have used various substrates entering at different steps of the glycolytic pathway (glucose, dihydroxyacetone) and the pentose phosphate pathway (xylitol). When compared with 5 mM glucose, 25 mM glucose induces a marked increase in both S14 and FAS gene expression, detectable as early as 2 h and peaking at 6 h. Increasing concentrations (1-5 mM) of xylitol and dihydroxyacetone in the presence of 5 mM glucose are also able to induce S14 and FAS gene expression progressively. Among the various glucose metabolites measured, glucose 6-phosphate, in contrast with xylulose 5-phosphate and metabolites of the lower part of glycolysis, is the only one that shows a clear-cut parallelism between its concentration and the degree of S14 and FAS gene expression. We conclude that glucose 6-phosphate is the most likely signal metabolite for the glucose-induced transcription of this group of genes.
MeSH Terms
Aging
Animals
Cells, Cultured
Dihydroxyacetone/pharmacology
Enzyme Induction/drug effects,genetics
Fatty Acid Synthases/biosynthesis,drug effects,genetics
Female
Gene Expression Regulation/drug effects
Glucokinase/metabolism
Glucose/pharmacology
Glucose-6-Phosphate/metabolism
Glycolysis/drug effects
Liver/drug effects,enzymology,metabolism
Nuclear Proteins
Proteins/drug effects,genetics
Rats
Rats, Wistar
Transcription Factors
Xylitol/pharmacology
Chemicals
Nuclear Proteins
Proteins
THRSP protein, human
Thrsp protein, rat
Transcription Factors
Glucose-6-Phosphate
Fatty Acid Synthases
Glucokinase
Glucose
Dihydroxyacetone
Xylitol
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mourrieras F
U342 INSERM, Hôpital Saint-Vincent-de-Paul, Paris, France.
Foufelle F
Foretz M
Morin J
Bouche S
Ferre P
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