Literature DB >> 6721851

Altered metabolic states do not change the intracellular distribution of hexokinase in Zajdela hepatoma ascites cells.

B D Nelson, F Kabir, P Muchiri.   

Abstract

The distribution of hexokinase between bound and soluble forms was studied by digitonin fractionation of Zajdela hepatoma ascites cells maintained under various metabolic conditions. Addition of glucose to Zajdela cells respiring on endogenous substrates induces an immediate inhibition of respiration by 50-60% ( Crabtree effect), and a production of acid due to glycolysis. Acid production decreases abruptly after 60s to 50% of the initial rate. The ATP/ADP ratio is not altered by the addition of glucose or by different rates of glycolysis. The uncoupling agent carbonyl cyanide m-chlorophenylhydrazone decreases the ATP/ADP ratio by 10-fold in cells respiring on endogenous substrate, but has little effect on cells oxidizing glucose. Rapid fractionation of the cells under these various metabolic conditions revealed no change in the distribution of hexokinase. Approx. 75% of hexokinase is bound in all cases, in contrast with lactate dehydrogenase, 95% of which was in the soluble form. Longer-term incubations (to 20 min) revealed only slight (10-15%) increases in soluble hexokinase in cells incubated with glucose. Various metabolic inhibitors had little additional affect on the subcellular distribution of hexokinase. Thus a rapid release of hexokinase from mitochondrial membrane is not a mechanism by which glycolysis is regulated in rapidly growing Zajdela hepatoma.

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Year:  1984        PMID: 6721851      PMCID: PMC1153460          DOI: 10.1042/bj2190159

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  25 in total

1.  Spectroscopic evidence of metabolic control.

Authors:  B CHANCE; B HESS
Journal:  Science       Date:  1959-03-13       Impact factor: 47.728

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Authors:  P L Pedersen
Journal:  Prog Exp Tumor Res       Date:  1978

Review 3.  The hexokinases: kinetic, physical, and regulatory properties.

Authors:  D L Purich; H J Fromm; F B Rudolph
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1973

4.  Mitochondrial hexokinase. Release, rebinding, and location.

Authors:  I A Rose; J V Warms
Journal:  J Biol Chem       Date:  1967-04-10       Impact factor: 5.157

5.  Effects of energy metabolism on in vivo distribution of hexokinase in brain.

Authors:  H R Knull; W F Taylor; W W Wells
Journal:  J Biol Chem       Date:  1973-08-10       Impact factor: 5.157

6.  Phosphate mediation of the Crabtree and Pasteur effects.

Authors:  D H Koobs
Journal:  Science       Date:  1972-10-13       Impact factor: 47.728

7.  The effect of oestrogen on the activity and binding of multiple forms of hexokinase in the rat uterus.

Authors:  N A Baquer; P McLean
Journal:  Biochem Biophys Res Commun       Date:  1969-09-24       Impact factor: 3.575

8.  A possible interrelationship between binding of hexokinase and the site of ATP formation in Krebs ascites cells.

Authors:  K A Gumaa; P McLean
Journal:  Biochem Biophys Res Commun       Date:  1969-08-22       Impact factor: 3.575

9.  Sequential control of hexokinase in ascites cells.

Authors:  K A Gumaa; P McLean
Journal:  Biochem Biophys Res Commun       Date:  1969-06-27       Impact factor: 3.575

10.  Enzymatic properties of the inner and outer membranes of rat liver mitochondria.

Authors:  C Schnaitman; J W Greenawalt
Journal:  J Cell Biol       Date:  1968-07       Impact factor: 8.077

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  3 in total

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Journal:  Biochem J       Date:  1996-02-15       Impact factor: 3.857

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Authors:  Peter L Pedersen
Journal:  J Bioenerg Biomembr       Date:  2007-06       Impact factor: 2.945

3.  Interplay between cytoplasmic Ca2+ and the ATP/ADP ratio: a feedback control mechanism in mouse pancreatic islets.

Authors:  P Detimary; P Gilon; J C Henquin
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  3 in total

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