Loading…
Insulin regulation of pyruvate kinase activity in isolated adipocytes. Crucial role of glucose and the hexosamine biosynthesis pathway in the expression of insulin action
We recently identified glutamine:fructose-6-phosphate amidotransferase (GFAT) as an insulin-regulated enzyme in adipocytes. Moreover, we found that loss of GFAT activity is not due to a direct action of insulin but rather is mediated by enhanced glucose uptake and the subsequent routing of glucose t...
Saved in:
Published in: | The Journal of biological chemistry 1992-05, Vol.267 (14), p.9718-9723 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | We recently identified glutamine:fructose-6-phosphate amidotransferase (GFAT) as an insulin-regulated enzyme in adipocytes.
Moreover, we found that loss of GFAT activity is not due to a direct action of insulin but rather is mediated by enhanced
glucose uptake and the subsequent routing of glucose through the hexosamine biosynthesis pathway. To assess whether other
cytosolic enzymes are controlled through formation of hexosamine products, we treated adipocytes for 5 h with physiological
concentrations of insulin (ED50 = 0.33 ng/ml), glucose (ED50 = 4.5 mM), and glutamine (ED50 = 4.4 mM) and then measured pyruvate
kinase (PK) activity. Combined treatment resulted in a progressive (t 1/2 of 2.5 h) and marked (3-fold) increase in PK activity,
whereas omission of one or more of these components failed to alter enzyme activity. Several lines of additional evidence
implicated the hexosamine biosynthesis pathway in PK regulation; therefore, it appears that the M2 isoform of pyruvate kinase
represents another enzyme regulated by insulin through stimulation of glucose uptake and formation of hexosamine products.
Related studies revealed that enhancement of PK activity is dependent upon ongoing mRNA synthesis and de novo protein synthesis
and is mediated by an increase in enzyme content. Considered together, these findings provide new insights into the cascade
of metabolic events triggered by insulin and implicated a novel metabolic pathway in the pretranslational control of enzyme
function. |
---|---|
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/s0021-9258(19)50150-8 |