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Heritability of glutathione and related metabolites in stored red blood cells

Authors :
Thomas J. van ‘t Erve
Kelli K. Ryckman
Jeffrey C. Murray
Benjamin W. Darbro
Brett A. Wagner
Claire M. Doskey
Garry R. Buettner
Thomas J. Raife
John R. Hess
Source :
Free Radical Biology and Medicine. 76:107-113
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

Red blood cells (RBCs) collected for transfusion deteriorate during storage. This deterioration is termed the "RBC storage lesion." There is increasing concern over the safety, therapeutic efficacy, and toxicity of transfusing longer-stored units of blood. The severity of the RBC storage lesion is dependent on storage time and varies markedly between individuals. Oxidative damage is considered a significant factor in the development of the RBC storage lesion. In this study, the variability during storage and heritability of antioxidants and metabolites central to RBC integrity and function were investigated. In a classic twin study, we determined the heritability of glutathione (GSH), glutathione disulfide (GSSG), the status of the GSSG,2H(+)/2GSH couple (Ehc), and total glutathione (tGSH) in donated RBCs over 56 days of storage. Intracellular GSH and GSSG concentrations both decrease during storage (median net loss of 0.52 ± 0.63 mM (median ± SD) and 0.032 ± 0.107 mM, respectively, over 42 days). Taking into account the decline in pH, Ehc became more positive (oxidized) during storage (median net increase of 35 ± 16 mV). In our study population heritability estimates for GSH, GSSG, tGSH, and Ehc measured over 56 days of storage are 79, 60, 67, and, 75%, respectively. We conclude that susceptibility of stored RBCs to oxidative injury due to variations in the GSH redox buffer is highly variable among individual donors and strongly heritable. Identifying the genes that regulate the storage-related changes in this redox buffer could lead to the development of new methods to minimize the RBC storage lesion.

Details

ISSN :
08915849
Volume :
76
Database :
OpenAIRE
Journal :
Free Radical Biology and Medicine
Accession number :
edsair.doi.dedup.....e6e16f2650f50fb95f796fbe5e1e1442
Full Text :
https://doi.org/10.1016/j.freeradbiomed.2014.07.040