Cargando…

Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity

Red blood cell (RBC) storage in the blood bank promotes the progressive accumulation of metabolic alterations that may ultimately impact the erythrocyte capacity to cope with oxidant stressors. However, the metabolic underpinnings of the capacity of RBC to resist oxidant stress and the potential imp...

Descripción completa

Detalles Bibliográficos
Autores principales: D’Alessandro, Angelo, Fu, Xiaoyun, Kanias, Tamir, Reisz, Julie A., Culp-Hill, Rachel, Guo, Yuelong, Gladwin, Mark T., Page, Grier, Kleinman, Steve, Lanteri, Marion, Stone, Mars, Busch, Michael P., Zimring, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094095/
https://www.ncbi.nlm.nih.gov/pubmed/32241843
http://dx.doi.org/10.3324/haematol.2020.246603
_version_ 1783687946505814016
author D’Alessandro, Angelo
Fu, Xiaoyun
Kanias, Tamir
Reisz, Julie A.
Culp-Hill, Rachel
Guo, Yuelong
Gladwin, Mark T.
Page, Grier
Kleinman, Steve
Lanteri, Marion
Stone, Mars
Busch, Michael P.
Zimring, James C.
author_facet D’Alessandro, Angelo
Fu, Xiaoyun
Kanias, Tamir
Reisz, Julie A.
Culp-Hill, Rachel
Guo, Yuelong
Gladwin, Mark T.
Page, Grier
Kleinman, Steve
Lanteri, Marion
Stone, Mars
Busch, Michael P.
Zimring, James C.
author_sort D’Alessandro, Angelo
collection PubMed
description Red blood cell (RBC) storage in the blood bank promotes the progressive accumulation of metabolic alterations that may ultimately impact the erythrocyte capacity to cope with oxidant stressors. However, the metabolic underpinnings of the capacity of RBC to resist oxidant stress and the potential impact of donor biology on this phenotype are not known. Within the framework of the REDS-III RBC-Omics study, RBC from 8,502 healthy blood donors were stored for 42 days and tested for their propensity to hemolyse following oxidant stress. A subset of extreme hemolysers donated a second unit of blood, which was stored for 10, 23, and 42 days and profiled again for oxidative hemolysis and metabolomics (599 samples). Alterations of RBC energy and redox homeostasis were noted in donors with high oxidative hemolysis. RBC from females, donors over 60 years old, donors of Asian/South Asian race-ethnicity, and RBC stored in additive solution- 3 were each independently characterized by improved antioxidant metabolism compared to, respectively, males, donors under 30 years old, Hispanic and African American race ethnicity donors, and RBC stored in additive solution-1. Merging metabolomics data with results from an independent genome-wide association study on the same cohort, we identified metabolic markers of hemolysis and glucose 6-phosphate dehydrogenasedeficiency, which were associated with extremes in oxidative hemolysis and dysregulation in nicotinamide adenine dinucleotide phosphate and glutathione- dependent detoxification pathways of oxidized lipids. Donor sex, age, ethnicity, additive solution and glucose 6-phosphate dehydrogenase status impact the metabolism of the stored erythrocyte and its susceptibility to hemolysis following oxidative insults.
format Online
Article
Text
id pubmed-8094095
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Fondazione Ferrata Storti
record_format MEDLINE/PubMed
spelling pubmed-80940952021-05-06 Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity D’Alessandro, Angelo Fu, Xiaoyun Kanias, Tamir Reisz, Julie A. Culp-Hill, Rachel Guo, Yuelong Gladwin, Mark T. Page, Grier Kleinman, Steve Lanteri, Marion Stone, Mars Busch, Michael P. Zimring, James C. Haematologica Article Red blood cell (RBC) storage in the blood bank promotes the progressive accumulation of metabolic alterations that may ultimately impact the erythrocyte capacity to cope with oxidant stressors. However, the metabolic underpinnings of the capacity of RBC to resist oxidant stress and the potential impact of donor biology on this phenotype are not known. Within the framework of the REDS-III RBC-Omics study, RBC from 8,502 healthy blood donors were stored for 42 days and tested for their propensity to hemolyse following oxidant stress. A subset of extreme hemolysers donated a second unit of blood, which was stored for 10, 23, and 42 days and profiled again for oxidative hemolysis and metabolomics (599 samples). Alterations of RBC energy and redox homeostasis were noted in donors with high oxidative hemolysis. RBC from females, donors over 60 years old, donors of Asian/South Asian race-ethnicity, and RBC stored in additive solution- 3 were each independently characterized by improved antioxidant metabolism compared to, respectively, males, donors under 30 years old, Hispanic and African American race ethnicity donors, and RBC stored in additive solution-1. Merging metabolomics data with results from an independent genome-wide association study on the same cohort, we identified metabolic markers of hemolysis and glucose 6-phosphate dehydrogenasedeficiency, which were associated with extremes in oxidative hemolysis and dysregulation in nicotinamide adenine dinucleotide phosphate and glutathione- dependent detoxification pathways of oxidized lipids. Donor sex, age, ethnicity, additive solution and glucose 6-phosphate dehydrogenase status impact the metabolism of the stored erythrocyte and its susceptibility to hemolysis following oxidative insults. Fondazione Ferrata Storti 2020-04-02 /pmc/articles/PMC8094095/ /pubmed/32241843 http://dx.doi.org/10.3324/haematol.2020.246603 Text en Copyright© 2021 Ferrata Storti Foundation https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
D’Alessandro, Angelo
Fu, Xiaoyun
Kanias, Tamir
Reisz, Julie A.
Culp-Hill, Rachel
Guo, Yuelong
Gladwin, Mark T.
Page, Grier
Kleinman, Steve
Lanteri, Marion
Stone, Mars
Busch, Michael P.
Zimring, James C.
Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
title Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
title_full Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
title_fullStr Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
title_full_unstemmed Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
title_short Donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
title_sort donor sex, age and ethnicity impact stored red blood cell antioxidant metabolism through mechanisms in part explained by glucose 6-phosphate dehydrogenase levels and activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094095/
https://www.ncbi.nlm.nih.gov/pubmed/32241843
http://dx.doi.org/10.3324/haematol.2020.246603
work_keys_str_mv AT dalessandroangelo donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT fuxiaoyun donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT kaniastamir donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT reiszjuliea donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT culphillrachel donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT guoyuelong donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT gladwinmarkt donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT pagegrier donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT kleinmansteve donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT lanterimarion donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT stonemars donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT buschmichaelp donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity
AT zimringjamesc donorsexageandethnicityimpactstoredredbloodcellantioxidantmetabolismthroughmechanismsinpartexplainedbyglucose6phosphatedehydrogenaselevelsandactivity