ADENOVIRUS-MEDIATED OVEREXPRESSION OF LIVER 6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE IN GLUCONEOGENIC RAT HEPATOMA-CELLS - PARADOXICAL EFFECT ON FRU-2,6-P(2) LEVELS

被引:33
作者
ARGAUD, D
LANGE, AJ
BECKER, TC
OKAR, DA
ELMAGHRABI, MR
NEWGARD, CB
PILKIS, SJ
机构
[1] SUNY STONY BROOK,HLTH SCI CTR,DEPT PHYSIOL & BIOPHYS,STONY BROOK,NY 11794
[2] UNIV TEXAS,SW MED CTR,DEPT BIOCHEM & INTERNAL MED,DALLAS,TX 75235
关键词
D O I
10.1074/jbc.270.41.24229
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
6-Phosphofructo-2-kinase/fructose-2,6-bisphosphatase has been postulated 60 be a metabolic signaling enzyme, which acts as a switch between glycolysis and gluconeogenesis in mammalian liver by regulating the level of fructose 2,6-bisphosphate, The effect of overexpressing the bifunctional enzyme was studied in FAO cells transduced with recombinant adenoviral constructs of either the wild-type enzyme or a double mutant that has no bisphosphatase activity or protein kinase phosphorylation site, With both constructs, the mRNA and protein were overexpressed by 150- and 40-fold, respectively, Addition of cAMP to cells overexpressing the wild-type enzyme increased the S-0.5 for fructose 6-phosphate of the kinase by 1.5 fold but had no effect on the overexpressed double mutant, When the wild-type enzyme was overexpressed, there was a decrease in fructose 2,6-bisphosphate levels, even though 6-phosphofructo-2-kinase maximal activity increased more than 22 fold and was in excess of fructose 2,6-bisphosphatase maximal activity, The kinase:bisphosphatase maximal activity ratio was decreased, indicating that the overexpressed enzyme was phosphorylated by cAMP-dependent protein kinase, Overexpression of the double mutant resulted in a 28-fold increase in kinase maximal activity and a 3-4 fold increase in fructose 2,6-bisphosphate levels, Overexpression of this form inhibited the rate of glucose production from dihydroxyacetone by 90% and stimulated the rate of lactate plus pyruvate production by 200%, In contrast, overexpression of the wild-type enzyme enhanced glucose production and inhibited lactate plus pyruvate production, These results provide direct support for fructose 2,6-bisphosphate as a regulator of gluconeogenic/glycolytic pathway flux and suggest that regulation of bifunctional enzyme activities by covalent modification is more important than the amount of the protein.
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页码:24229 / 24236
页数:8
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