Levels of red blood cells derived microparticles in stored erythrocyte concentrate
Author(s) -
Rana Maheen,
Yasir Arfat,
Naseem Omar,
Mazari Nazish,
Manzoor Navida,
Salman Aziz Rao,
Muhammad Rashid,
Mohsin Shahida
Publication year - 2020
Publication title -
african journal of pharmacy and pharmacology
Language(s) - English
Resource type - Journals
ISSN - 1996-0816
DOI - 10.5897/ajpp2020.5126
Subject(s) - annexin , flow cytometry , phosphatidylserine , andrology , centrifugation , red blood cell , chemistry , microparticle , blood transfusion , blood preservation , whole blood , antibody , medicine , immunology , chromatography , biology , biochemistry , phospholipid , membrane , astrobiology
There is increasing evidence of the clinical importance of microparticles (MPs) and their role in blood transfusion-related side effects and the transmission of pathogens. The study aims to examine the red blood cell-derived MPs in blood bags during storage under standardized blood bank conditions. The samples were tested at various times to demonstrate the presence of RBC-derived MPs by flow cytometry. The quantitative assay was carried out in stored erythrocyte concentrate on days 0, 25 and 35 and their number from day 0 to 25 and 35 and the number of day 25 to day 35 were compared. The MPs were counted after being concentrated in a supernatant (labeled with the respective antibodies CD47, CD235a and Annexin V) obtained by a specific centrifugation procedure. The analysis showed that the number of Annexin V positive MPs increased between day 0 and day 35 (~ 0.001) and CD47 expression on MPs at day 25 and day 35 decreased compared to day 0 (~ 0.001). In addition, CD235a expression had shown minimal insignificant changes with an upward trend (> 0.05) during the storage period. It is concluded that monitoring the release of MPs from RBC units during storage is a sensitive approach to identifying MPs for transfusion drugs and, more broadly, for cell-based therapies. Key words: Red blood cells, phosphatidylserine, cell-derived microparticle.
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