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Phosphatidylethanolamine is progressively exposed in RBCs during storage
Author(s) -
Larson M. C.,
Karafin M. S.,
Hillery C. A.,
Hogg N.
Publication year - 2017
Publication title -
transfusion medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.471
H-Index - 59
eISSN - 1365-3148
pISSN - 0958-7578
DOI - 10.1111/tme.12382
Subject(s) - phosphatidylserine , phosphatidylethanolamine , flow cytometry , phospholipid , andrology , chemistry , red blood cell , phagocytosis , red cell , membrane , microbiology and biotechnology , immunology , biology , phosphatidylcholine , biochemistry , medicine
SUMMARY Background It is well established that as a blood unit ages, fewer of the unit's red blood cells (RBCs) remain in circulation post‐transfusion. The mechanism for clearance is not well defined. Phosphatidylethanolamine (PE) is a phospholipid that is primarily found on the inner leaflet of healthy cells, and is an important ligand for phagocytosis of dead cells when exposed. Objectives The objective of the present study was to measure the change in PE exposure in donor RBCs over increasing storage ages using the novel PE‐specific probe, duramycin. Methods Five adsol (AS‐1) preserved RBC units were sampled weekly for 6 weeks and were labelled with duramycin. The percentage of PE exposed on red cells in each sample was determined using flow cytometry. Surface phosphatidylserine (PS) was evaluated for comparison. Results We found that RBCs in AS‐preserved donor units increasingly exposed PE, from less than 1% in freshly processed RBCs, to nearly 20% at 42 days of storage and correlated with increased relative vesiculation or microparticle concentration and release of cell‐free haemoglobin. By comparison, only 5% of cells exposed PS at 42 days. Conclusion We conclude that exposure of PE in the RBC outer membrane was higher than that of PS during 42 days of storage and correlated significantly with increased vesiculation and release of haemoglobin.