Literature DB >> 3680497

Concentration of NADH-cytochrome b5 reductase in erythrocytes of normal and methemoglobinemic individuals measured with a quantitative radioimmunoblotting assay.

N Borgese1, G Pietrini, S Gaetani.   

Abstract

The activity of NADH-cytochrome b5 reductase (NADH-methemoglobin reductase) is generally reduced in red cells of patients with recessive hereditary methemoglobinemia. To determine whether this lower activity is due to reduced concentration of an enzyme with normal catalytic properties or to reduced activity of an enzyme present at normal concentration, we measured erythrocyte reductase concentrations with a quantitative radioimmunoblotting method, using affinity-purified polyclonal antibodies against rat liver microsomal reductase as probe. In five patients with the "mild" form of recessive hereditary methemoglobinemia, in which the activity of erythrocyte reductase was 4-13% of controls, concentrations of the enzyme, measured as antigen, were also reduced to 7-20% of the control values. The concentration of membrane-bound reductase antigen, measured in the ghost fraction, was similarly reduced. Thus, in these patients, the reductase deficit is caused mainly by a reduction in NADH-cytochrome b5 reductase concentration, although altered catalytic properties of the enzyme may also contribute to the reduced enzyme activity.

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Year:  1987        PMID: 3680497      PMCID: PMC442383          DOI: 10.1172/JCI113205

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  36 in total

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Journal:  Anal Biochem       Date:  1979-09-15       Impact factor: 3.365

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Authors:  N Borgese; S Gaetani
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4.  Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.

Authors:  D Choury; A Leroux; J C Kaplan
Journal:  J Clin Invest       Date:  1981-01       Impact factor: 14.808

5.  Biochemical mechanisms of glucose-6-phosphate dehydrogenase deficiency.

Authors:  A Morelli; U Benatti; G F Gaetani; A De Flora
Journal:  Proc Natl Acad Sci U S A       Date:  1978-04       Impact factor: 11.205

6.  Radioimmunochemical quantitation of human adenosine deaminase.

Authors:  P E Daddona; M A Frohman; W N Kelley
Journal:  J Clin Invest       Date:  1979-09       Impact factor: 14.808

7.  NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemia.

Authors:  D Lostanlen; G Lenoir; J C Kaplan
Journal:  J Clin Invest       Date:  1981-07       Impact factor: 14.808

8.  Localization and biosynthesis of NADH-cytochrome b5 reductase, an integral membrane protein, in rat liver cells. I. Distribution of the enzyme activity in microsomes, mitochondria, and golgi complex.

Authors:  N Borgese; J Meldolesi
Journal:  J Cell Biol       Date:  1980-06       Impact factor: 10.539

9.  Localization and biosynthesis of NADH-cytochrome b5 reductase, an integral membrane protein, in rat liver cells. II. Evidence that a single enzyme accounts for the activity in its various subcellular locations.

Authors:  J Meldolesi; G Corte; G Pietrini; N Borgese
Journal:  J Cell Biol       Date:  1980-06       Impact factor: 10.539

10.  Localization and biosynthesis of NADH-cytochrome b5 reductase, an iontegral membrane protein, in rat liver cells. III. Evidence for the independent insertion and turnover the enzyme in various subcellular compartments.

Authors:  N Borgese; G Pietrini; J Meldolesi
Journal:  J Cell Biol       Date:  1980-07       Impact factor: 10.539

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6.  A novel point mutation in a 3' splice site of the NADH-cytochrome b5 reductase gene results in immunologically undetectable enzyme and impaired NADH-dependent ascorbate regeneration in cultured fibroblasts of a patient with type II hereditary methemoglobinemia.

Authors:  K Shirabe; M T Landi; M Takeshita; G Uziel; E Fedrizzi; N Borgese
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

7.  Efficient Reduction of Vertebrate Cytoglobins by the Cytochrome b5/Cytochrome b5 Reductase/NADH System.

Authors:  Matthew B Amdahl; Courtney E Sparacino-Watkins; Paola Corti; Mark T Gladwin; Jesús Tejero
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  7 in total

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