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

被引:100
作者
Alessandro, Angelo D. [1 ,2 ,3 ]
Fu, Xiaoyun [4 ]
Kanias, Tamir [3 ,5 ]
Reisz, Julie A. [1 ]
Culp-Hill, Rachel [1 ]
Guo, Yuelong [6 ]
Gladwin, Mark T. [5 ]
Page, Grier [6 ]
Kleinman, Steven [7 ]
Lanteri, Marion [8 ]
Stone, Mars [8 ]
Busch, Michael P. [8 ]
Zimring, James C. [9 ]
机构
[1] Univ Colorado Denver, Dept Biochem & Mol Genet, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Univ Colorado Denver, Dept Med, Div Hematol, Anschutz Med Campus, Aurora, CO 80045 USA
[3] Vitalant Res Inst, Blood Syst Res Inst, Denver, CO 80230 USA
[4] Bloodworks Northwest Res Inst, Seattle, WA USA
[5] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[6] RTI Int, Atlanta, GA USA
[7] Univ British Columbia, Victoria, BC, Canada
[8] Vitalant Res Inst, Blood Syst Res Inst, San Francisco, CA USA
[9] Univ Virginia, Charlottesville, VA USA
关键词
SEVERE CONGENITAL NEUTROPENIA; TRANSCRIPTION FACTORS; MYELOID PROGENITOR; ZEBRAFISH MODEL; CSF3R MUTATIONS; HAX1; MUTATIONS; MESSENGER-RNA; PROTEIN; DISEASE; EXPRESSION;
D O I
10.3324/haematol.2020.246603
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Red blood cell (RBC) storage in the blood bank promotes the progres-sive 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 solu-tion-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 inde-pendent genome-wide association study on the same cohort, we identified metabolic markers of hemolysis and glucose 6-phosphate dehydrogenase-deficiency, which were associated with extremes in oxidative hemolysis and dysregulation in nicotinamide adenine dinucleotide phosphate and glu-tathione-dependent detoxification pathways of oxidized lipids. Donor sex, age, ethnicity, additive solution and glucose 6-phosphate dehydrogenase sta-tus impact the metabolism of the stored erythrocyte and its susceptibility to hemolysis following oxidative insults.
引用
收藏
页码:1290 / 1302
页数:13
相关论文
共 50 条
  • [1] Single-cell RNA-sequencing uncovers transcriptional states and fate decisions in haematopoiesis
    Athanasiadis, Emmanouil I.
    Botthof, Jan G.
    Andres, Helena
    Ferreira, Lauren
    Lio, Pietro
    Cvejic, Ana
    [J]. NATURE COMMUNICATIONS, 2017, 8
  • [2] Fish to Learn: Insights into Blood Development and Blood Disorders from Zebrafish Hematopoiesis
    Avagyan, Serine
    Zon, Leonard I.
    [J]. HUMAN GENE THERAPY, 2016, 27 (04) : 287 - 294
  • [3] Genetic Models of Leukemia in Zebrafish
    Baeten, Jeremy T.
    de Jong, Jill L. O.
    [J]. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2018, 6
  • [4] An artificial promoter construct for heat-inducible misexpression during fish embryogenesis
    Bajoghli, B
    Aghaallaei, N
    Heimbucher, T
    Czerny, T
    [J]. DEVELOPMENTAL BIOLOGY, 2004, 271 (02) : 416 - 430
  • [5] Zebrafish Granulocyte Colony-Stimulating Factor Receptor Maintains Neutrophil Number and Function throughout the Life Span
    Basheer, Faiza
    Rasighaemi, Parisa
    Liongue, Clifford
    Ward, Alister C.
    [J]. INFECTION AND IMMUNITY, 2019, 87 (02)
  • [6] Functional Integration of Newborn Neurons in the Zebrafish Optic Tectum
    Boulanger-Weill, Jonathan
    Sumbre, German
    [J]. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2019, 7
  • [7] HAX1 Mutations Causing Severe Congenital Neuropenia and Neurological Disease Lead to Cerebral Microstructural Abnormalities Documented by Quantitative MRI
    Boztug, Kaan
    Ding, Xiao-Qi
    Hartmann, Hans
    Ziesenitz, Lena
    Schaeffer, Alejandro A.
    Diestelhorst, Jana
    Pfeifer, Dietmar
    Appaswamy, Giridharan
    Kehbel, Sonja
    Simon, Thorsten
    Al Jefri, Abdullah
    Lanfermann, Heinrich
    Klein, Christoph
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (12) : 3157 - 3163
  • [8] Central nervous system involvement in severe congenital neutropenia:: neurological and neuropsychological abnormalities associated with specific HAX1 mutations
    Carlsson, G.
    van't Hooft, I.
    Melin, M.
    Entesarian, M.
    Laurencikas, E.
    Nennesmo, I.
    Trebinska, A.
    Grzybowska, E.
    Palmblad, J.
    Dahl, N.
    Nordenskjold, M.
    Fadeel, B.
    Henter, J-I
    [J]. JOURNAL OF INTERNAL MEDICINE, 2008, 264 (04) : 388 - 400
  • [9] Kostmann syndrome:: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myeloid progenitor cells
    Carlsson, G
    Aprikyan, AAG
    Tehranchi, R
    Dale, DC
    Porwit, A
    Hellström-Lindberg, E
    Palmblad, J
    Henter, JI
    Fadeel, B
    [J]. BLOOD, 2004, 103 (09) : 3355 - 3361
  • [10] Hax1 regulates neutrophil adhesion and motility through RhoA
    Cavnar, Peter J.
    Berthier, Erwin
    Beebe, David J.
    Huttenlocher, Anna
    [J]. JOURNAL OF CELL BIOLOGY, 2011, 193 (03) : 465 - 473