Literature DB >> 6661177

Branched-chain ketoacid dehydrogenase activity and growth of normal and mutant human fibroblasts: the effect of branched-chain amino acid concentration in culture medium.

D J Danner, J H Priest.   

Abstract

We investigated changes in cell growth and branched chain ketoacid dehydrogenase (BCKD) activity by varying the concentrations of branched-chain amino acids (BCAAs) in culture medium of diploid fibroblasts from humans with normal BCKD and with impaired enzyme function. For logarithmic growth the two cell populations required similar minimal concentrations (0.05 mM) for each of leucine, isoleucine, and valine tested together. At confluency (saturation density) mutant cells grew less well to the extent of 30 to 40% in the highest concentrations of BCAAs that could be tested, 20.8 mM. BCKD activity was not changed by growth of normal or mutant cells in the absence of BCAAs. This enzyme activity was increased in normal but not mutant cells by growth in 20.8 mM BCAAs. These studies suggest the following: (1) BCKD mutant fibroblasts in culture slow their growth rate in response to high concentrations of BCAAs; (2) the growth disadvantage for mutant cells in high concentrations of BCAAs may be useful to select for enzyme normal hybrids derived when cells with two different mutations affecting BCKD are fused; (3) the increase of BCKD activity in normal but not mutant cells grown in high concentrations of BCAAs can distinguish these phenotypes more precisely in humans; and (4) the mechanism of BCKD stimulation in normal cells grown in high concentrations of BCAAs remains to be explained but can be pursued further with the cell culture conditions described.

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Year:  1983        PMID: 6661177     DOI: 10.1007/bf00483948

Source DB:  PubMed          Journal:  Biochem Genet        ISSN: 0006-2928            Impact factor:   1.890


  24 in total

1.  Subcellular distribution and cofactor function of human branched chain alpha-ketoacid dehydrogenase in normal and mutant cultured skin fibroblasts.

Authors:  D J Danner; L J Elsas
Journal:  Biochem Med       Date:  1975-05

2.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

3.  Regulation of leucine and alpha-ketoisocaproate metabolism in skeletal muscle.

Authors:  S M Hutson; T C Cree; A E Harper
Journal:  J Biol Chem       Date:  1978-11-25       Impact factor: 5.157

4.  Inactivation of purified ox kidney branched-chain 2-oxoacid dehydrogenase complex by phosphorylation.

Authors:  H R Fatania; K S Lau; P J Randle
Journal:  FEBS Lett       Date:  1981-09-28       Impact factor: 4.124

5.  Influence of dietary nitrogen intake on mammalian branched chain alpha-keto acid dehydrogenase activity.

Authors:  S Hauschildt; J Lüthje; K Brand
Journal:  J Nutr       Date:  1981-12       Impact factor: 4.798

6.  Studies on the regulation of the branched chain alpha-keto acid dehydrogenase in the perfused rat liver.

Authors:  T B Patel; M S DeBuysere; L L Barron; M S Olson
Journal:  J Biol Chem       Date:  1981-09-10       Impact factor: 5.157

7.  Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts.

Authors:  S D Skaper; D P Molden; J E Seegmiller
Journal:  Biochem Genet       Date:  1976-08       Impact factor: 1.890

8.  Blood and tissue branched-chain amino and alpha-keto acid concentrations: effect of diet, starvation, and disease.

Authors:  S M Hutson; A E Harper
Journal:  Am J Clin Nutr       Date:  1981-02       Impact factor: 7.045

9.  Mechanism of the stimulation of branched chain oxoacid oxidation in liver by carnitine.

Authors:  M E May; R P Aftring; M G Buse
Journal:  J Biol Chem       Date:  1980-09-25       Impact factor: 5.157

10.  Effects of branched chain alpha-ketoacids on the metabolism of isolated rat liver cells. I. Regulation of branched chain alpha-ketoacid metabolism.

Authors:  J R Williamson; E Wałajtys-Rode; K E Coll
Journal:  J Biol Chem       Date:  1979-11-25       Impact factor: 5.157

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  3 in total

1.  On the mechanism of L-alloisoleucine formation: studies on a healthy subject and in fibroblasts from normals and patients with maple syrup urine disease.

Authors:  P Schadewaldt; H W Hammen; C Dalle-Feste; U Wendel
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Altered phosphorylation state of branched-chain 2-oxo acid dehydrogenase in a branched-chain acyltransferase deficient human fibroblast cell line.

Authors:  R S Eisenstein; G Hoganson; R H Miller; A E Harper
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Absence of branched chain acyl-transferase as a cause of maple syrup urine disease.

Authors:  D J Danner; N Armstrong; S C Heffelfinger; E T Sewell; J H Priest; L J Elsas
Journal:  J Clin Invest       Date:  1985-03       Impact factor: 14.808

  3 in total

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