Literature DB >> 3709569

Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria).

I Lombeck, U Wendel, J Versieck, L van Ballenberghe, H J Bremer, R Duran, S Wadman.   

Abstract

Manganese was measured in blood of a patient with prolidase deficiency by neutron activation analysis. The manganese content of packed blood cells was 48.9 ng/g wet weight (controls 18.4 +/- 4.3 ng/g wet weight). It was proportionately increased in whole blood, whereas the serum manganese concentration was unchanged. The erythrocyte arginase activity was reduced to 46% of the mean control value. The reduced activities of two manganese-dependent enzymes, prolidase and arginase in erythrocytes in combination with an increased manganese content cannot be explained at the moment and leads to the speculation that manganese is inaccessible for enzyme activation.

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Year:  1986        PMID: 3709569     DOI: 10.1007/bf00496038

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  11 in total

1.  Studies on a patient with iminopeptiduria. I. Identification of urinary iminopeptides.

Authors:  H Kodama; S Umemura; M Shimomura; S Mizuhara; J Arata; Y Yamamoto; A Yasutake; N Izumiya
Journal:  Physiol Chem Phys       Date:  1976

2.  Manganese, copper, and zinc concentrations in serum and packed blood cells during acute hepatitis, chronic hepatitis, and posthepatitic cirrhosis.

Authors:  J Versieck; F Barbier; A Speecke; J Hoste
Journal:  Clin Chem       Date:  1974-09       Impact factor: 8.327

3.  A prolidase deficiency in man with iminopeptiduria.

Authors:  G F Powell; M A Rasco; R M Maniscalco
Journal:  Metabolism       Date:  1974-06       Impact factor: 8.694

4.  Determination of manganese, copper and zinc in serum and packed blood cells by neutron activation analysis. Studies on the metabolism of trace elements.

Authors:  J Versieck; A Speecke; J Hoste; F Barbier
Journal:  Z Klin Chem Klin Biochem       Date:  1973-05

5.  A syndrome resembling lathyrism associated with iminodipeptiduria.

Authors:  S I Goodman; C C Solomons; F Muschenheim; C A McIntyre; B Miles; D O'Brien
Journal:  Am J Med       Date:  1968-07       Impact factor: 4.965

6.  Studies on a patient with iminodipeptiduria. II. Lack of prolidase activity in blood cells.

Authors:  S Umemura
Journal:  Physiol Chem Phys       Date:  1978

7.  Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues.

Authors:  W Endres; R Schaller; Y S Shin
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

8.  Substrate specificity of manganese-activated prolidase in control and prolidase-deficient cultured skin fibroblasts.

Authors:  J Butterworth; D Priestman
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

9.  Optimal conditions for prolidase assay by proline colorimetric determination: application to iminodipeptiduria.

Authors:  I Myara; C Charpentier; A Lemonnier
Journal:  Clin Chim Acta       Date:  1982-10-27       Impact factor: 3.786

10.  In-vitro responses to ascorbate and manganese in fibroblasts from a patient with prolidase deficiency and iminodipeptiduria: cell growth, prolidase activity and collagen metabolism.

Authors:  I Myara; C Charpentier; C Wolfrom; M Gautier; A Lemonnier; M Larregue; A Chamson; J Frey
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

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  6 in total

1.  Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.

Authors:  F Endo; A Tanoue; A Kitano; J Arata; D M Danks; C M Lapière; Y Sei; S K Wadman; I Matsuda
Journal:  J Clin Invest       Date:  1990-01       Impact factor: 14.808

2.  Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine.

Authors:  S H Moolenaar; U F Engelke; N G Abeling; H Mandel; M Duran; R A Wevers
Journal:  J Inherit Metab Dis       Date:  2001-12       Impact factor: 4.982

3.  A single nucleotide change in the prolidase gene in fibroblasts from two patients with polypeptide positive prolidase deficiency. Expression of the mutant enzyme in NIH 3T3 cells.

Authors:  A Tanoue; F Endo; A Kitano; I Matsuda
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

4.  Prolidase Deficiency in a Mexican-American Patient Identified by Array CGH Reveals a Novel and the Largest PEPD Gene Deletion.

Authors:  Jonathan P Hintze; Amelia Kirby; Erin Torti; Jacqueline R Batanian
Journal:  Mol Syndromol       Date:  2016-04-14

Review 5.  Clinical Genetics of Prolidase Deficiency: An Updated Review.

Authors:  Marta Spodenkiewicz; Michel Spodenkiewicz; Maureen Cleary; Marie Massier; Giorgos Fitsialos; Vincent Cottin; Guillaume Jouret; Céline Poirsier; Martine Doco-Fenzy; Anne-Sophie Lèbre
Journal:  Biology (Basel)       Date:  2020-05-21

6.  Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases.

Authors:  Francis Rossignol; Marvid S Duarte Moreno; Carlos R Ferreira; Manuel Schiff; Jean-François Benoist; Manfred Boehm; Emmanuelle Bourrat; Aline Cano; Brigitte Chabrol; Claudine Cosson; José Luís Dapena Díaz; Arthur D'Harlingue; David Dimmock; Alexandra F Freeman; María Tallón García; Cheryl Garganta; Tobias Goerge; Sara S Halbach; Jan de Laffolie; Christina T Lam; Ludovic Martin; Esmeralda Martins; Andrea Meinhardt; Isabelle Melki; Amanda K Ombrello; Noémie Pérez; Dulce Quelhas; Anna Scott; Anne M Slavotinek; Ana Rita Soares; Sarah L Stein; Kira Süßmuth; Jenny Thies
Journal:  Genet Med       Date:  2021-05-26       Impact factor: 8.822

  6 in total

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