Enzymatic Changes in Red Blood Cells of Diamond-Blackfan Anemia.


Journal

The Tohoku journal of experimental medicine
ISSN: 1349-3329
Titre abrégé: Tohoku J Exp Med
Pays: Japan
ID NLM: 0417355

Informations de publication

Date de publication:
09 2021
Historique:
entrez: 16 9 2021
pubmed: 17 9 2021
medline: 9 10 2021
Statut: ppublish

Résumé

Diamond-Blackfan anemia is a congenital bone marrow failure syndrome characterized by red blood cell (RBC) aplasia with varied malformations in infants. Elevated activity of adenosine deaminase (ADA) has been considered as a useful biomarker of Diamond-Blackfan anemia, and ADA assay has been shown to be more sensitive than genetic diagnosis. Approximately, 80% of the examined patients showed elevated ADA activity, whereas genetic tests of ribosome subunit genes identified mutations in approximately 60% of the patients. We previously reported that reduced glutathione (GSH) levels in RBCs may serve as a biomarker of Diamond-Blackfan anemia. In this study, to confirm the universality of our data, we extended the analysis to seven RBC enzymes and GSH of 14 patients with Diamond-Blackfan anemia and performed a cross-analysis study using enzyme activity assay and recently reported proteome data. Statistical analysis revealed that both data exhibited high similarity, upregulation in the hexokinase and pentose-phosphate pathway, and downregulation in glycolytic enzymes such as phosphofructokinase and pyruvate kinase, in the RBCs obtained from the subjects with Diamond-Blackfan anemia. The only discrepancy between enzyme activity and proteome data was observed in glucose-6-phosphate dehydrogenase (G6PD), as increased G6PD activity showed no relation with the significant elevation in protein levels. These results suggest that our enzymatic activity data of Diamond-Blackfan anemia are universal and that the enzymatic activation of G6PD via a hitherto-unveiled mechanism is another metabolic feature of RBCs of Diamond-Blackfan anemia.

Identifiants

pubmed: 34526430
doi: 10.1620/tjem.255.49
doi:

Substances chimiques

Biomarkers 0
Glucosephosphate Dehydrogenase EC 1.1.1.49
Aminohydrolases EC 3.5.4.-
adenine deaminase EC 3.5.4.2
Glutathione GAN16C9B8O

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

49-55

Auteurs

Taiju Utsugisawa (T)

Department of Transfusion Medicine and Cell Processing, Faculty of Medicine, Tokyo Women's Medical University.

Toshitaka Uchiyama (T)

Institute of Medical Genetics, Tokyo Women's Medical University.

Tsutomu Toki (T)

Department of Pediatrics, Hirosaki University, School of Medicine.

Keiko Shimojima-Yamamoto (K)

Department of Transfusion Medicine and Cell Processing, Faculty of Medicine, Tokyo Women's Medical University.
Institute of Medical Genetics, Tokyo Women's Medical University.

Shouichi Ohga (S)

Department of Pediatrics, Kyushu University, School of Medicine.

Etsuro Ito (E)

Department of Pediatrics, Hirosaki University, School of Medicine.

Hitoshi Kanno (H)

Department of Transfusion Medicine and Cell Processing, Faculty of Medicine, Tokyo Women's Medical University.
Institute of Medical Genetics, Tokyo Women's Medical University.

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Classifications MeSH