Whole blood storage in CPDA1 blood bags alters erythrocyte membrane proteome

Al-Thani, Amna Mohamed; Voss, Sven Christian; Al-Menhali, Afnan Saleh; Barcaru, Andrei; Horvatovich, Peter; Al Jaber, Hind; Nikolovski, Zoran; Latiff, Aishah; Georgakopoulos, Costas; Merenkov, Zeyd; Segura Noguera, Jordi; Alsayrafi, Mohammed; Jaganjac, Morana

doi:http://dx.doi.org/10.1155/2018/6375379

Whole blood storage in CPDA1 blood bags alters erythrocyte membrane proteome

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Al-Thani AM, Voss SC, Al-Menhali AS, Barcaru A, Horvatovich P, Al Jaber H, Nikolovski Z, Latiff A, Georgakopoulos C, Merenkov Z, Segura J, Alsayrafi M, Jaganjac M. Whole blood storage in CPDA1 blood bags alters erythrocyte membrane proteome. Oxid Med Cell Longev. 2018; 2018:6375379. DOI 10.1155/2018/6375379

Abstract

Autologous blood transfusion (ABT) has been frequently abused in endurance sport and is prohibited since the mid-1980s by the International Olympic Committee. Apart from any significant performance-enhancing effects, the ABT may pose a serious health issue due to aging erythrocyte-derived "red cell storage lesions." The current study investigated the effect of blood storage in citrate phosphate dextrose adenine (CPDA1) on the red blood cell (RBC) membrane proteome. One unit of blood was collected in CPDA1 blood bags from 6 healthy female volunteers. RBC membrane protein samples were prepared on days 0, 14, and 35 of storage. Proteins were digested in gel and peptides separated by nanoliquid chromatography coupled to tandem mass spectrometry resulting in the confident identification of 33 proteins that quantitatively change during storage. Comparative proteomics suggested storage-induced translocation of cytoplasmic proteins to the membrane while redox proteomics analysis identified 14 proteins prone to storage-induced oxidation. The affected proteins are implicated in the RBC energy metabolism and membrane vesiculation and could contribute to the adverse posttransfusion outcomes. Spectrin alpha chain, band 3 protein, glyceraldehyde-3-phosphate dehydrogenase, and ankyrin-1 were the main proteins affected by storage. Although potential biomarkers of stored RBCs were identified, the stability and lifetime of these markers posttransfusion remain unknown. In summary, the study demonstrated the importance of studying storage-induced alterations in the erythrocyte membrane proteome and the need to understand the clearance kinetics of transfused erythrocytes and identified protein markers.