Literature DB >> 35236

Inactive 3-hydroxy-3-methylglutaryl-coenzyme A reductase in broken cell preparations of various mammalian tissues and cell cultures.

S E Saucier, A A Kandutsch.   

Abstract

Preincubation of broken cell preparations from a variety of tissues and cell cultures resulted in an apparent increase in the level of 3-hydroxy-3-methylglutaryl-CoA reductase activity. However, apparent activation of the reductase in mouse liver, hepatomas and primary liver cell cultures was attributed largely to the loss, during the preincubation period, of an interfering enzyme, 3-hydroxy-3-methylglutaryl-CoA lyase. Among non hepatic cells and tissues (which did not contain appreciable lyase activity) the proportion of latent reductase was high in sonicates of fetal brain and in L cells and was independent of the level of total enzyme activity present. Activation of the reductase was blocked by hydroxymethylglutaryl-CoA and NADPH as well as by KF so that activation did not occur under the conditions of the enzyme assay. The enzyme was activated slowly at 4 degrees C, so that partial activation of the latent form occurred during isolation of the microsomal fraction by differential centrifugation. The reductase present in sonicates of cells with either a high or low proportion of the latent enzyme was inactivated by incubation with ATP and Mg2+. Suppression of reductase activity in L cell cultures by treatment with 25-hydroxycholesterol and an age-related decline in brain enzyme activity did not involve reversible conversion of the reductase to an inactive form.

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Year:  1979        PMID: 35236     DOI: 10.1016/0005-2760(79)90162-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

1.  Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase.

Authors:  G C Ness
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

2.  Inhibition of sterol biosynthesis by 14 alpha-hydroxy-delta 7-sterols.

Authors:  G J Schroepfer; R A Pascal; A A Kandutsch
Journal:  Experientia       Date:  1980-05-15

3.  Independent regulation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase and chylomicron remnant receptor activities in rat liver.

Authors:  D P Wade; A K Soutar; G F Gibbons
Journal:  Biochem J       Date:  1984-02-15       Impact factor: 3.857

4.  The role of substrate supply in the regulation of cholesterol biosynthesis in rat hepatocytes.

Authors:  C R Pullinger; G F Gibbons
Journal:  Biochem J       Date:  1983-03-15       Impact factor: 3.857

5.  Activity of 3-hydroxy-3-methylglutaryl-coenzyme A reductase does not respond to ubiquinone uptake in cultured cells.

Authors:  W A Maltese; J R Aprille; R A Green
Journal:  Biochem J       Date:  1987-09-01       Impact factor: 3.857

6.  Diurnal variations in the effects of an unsaturated-fat-containing diet on fatty acid and cholesterol synthesis in rat hepatocytes.

Authors:  G F Gibbons; C R Pullinger
Journal:  Biochem J       Date:  1986-11-01       Impact factor: 3.857

7.  Regulation of cholesterol synthesis in the liver and mammary gland of the lactating rat.

Authors:  G F Gibbons; C R Pullinger; M R Munday; D H Williamson
Journal:  Biochem J       Date:  1983-06-15       Impact factor: 3.857

8.  Lethal effect of cis- but not trans-22-dehydrocholesterol on mouse fibroblast cells.

Authors:  H W Kircher; F U Rosenstein; A A Kandutsch
Journal:  Lipids       Date:  1981-12       Impact factor: 1.880

9.  Changes in sterol biosynthesis accompanying cessation of glial cell growth in serum-free medium.

Authors:  W A Maltese; B A Reitz; J J Volpe
Journal:  Biochem J       Date:  1980-11-15       Impact factor: 3.857

10.  3-Hydroxy-3-methylglutaryl coenzyme A reductase localization in rat liver peroxisomes and microsomes of control and cholestyramine-treated animals: quantitative biochemical and immunoelectron microscopical analyses.

Authors:  G A Keller; M Pazirandeh; S Krisans
Journal:  J Cell Biol       Date:  1986-09       Impact factor: 10.539

  10 in total

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