Storage-dependent remodeling of the red blood cell membrane is associated with increased immunoglobulin G binding, lipid raft rearrangement, and caspase activation
Anastasios G. Kriebardis
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorMarianna H. Antonelou
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorKonstantinos E. Stamoulis
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorEffrosini Economou-Petersen
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorLukas H. Margaritis
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorIssidora S. Papassideri
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorAnastasios G. Kriebardis
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorMarianna H. Antonelou
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorKonstantinos E. Stamoulis
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorEffrosini Economou-Petersen
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorLukas H. Margaritis
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorIssidora S. Papassideri
From the Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Panepistimiopolis; and the National Blood Center, Athens, Greece.
Search for more papers by this authorThis study was partly supported by the Empeirikeion Foundation and the Special Account for Research Grants of the University of Athens to ISP. AGK thanks the Hellenic State Scholarship Foundation for the award of the PhD fellowship.
Abstract
BACKGROUND: The elucidation of the storage lesion is important for the improvement of red blood cell (RBC) storage. Ex vivo storage is also a model system for studying cell-signaling events in the senescence and programmed cell death of RBCs. The membrane hosts critical steps in these mechanisms and undergoes widespread remodeling over the storage period.
STUDY DESIGN AND METHODS: Fresh and CPDA-stored RBCs from 21 blood donors were evaluated as whole cells, membrane ghosts, and cytoskeletons by sodium dodecyl sulfate–polyacrylamide gel electrophoresis, immunoblotting, immunofluorescence microscopy, and in situ assays. Band 3 content, immunoglobulin G (IgG) content, specific protein movement to and from the membrane, and caspase system activation were measured.
RESULTS: During storage, Band 3 protein was aggregated and its content decreased as did the content of several lipid raft–related proteins. IgG binding to the membrane increased. Sorcin and synexin moved from the cytosol to the membrane, stomatin and flotillins left the membrane, the Fas protein was oligomerized, and caspase was activated.
CONCLUSION: The remodeling of the RBC membrane during storage includes loss and oxidative cross-linking of Band 3 as well as IgG binding. This process occurs with lipid raft development and loss and is probably driven by caspase activation. Oxidative injury appears to be an important driver of RBC aging during storage.
REFERENCES
- 1 Kuypers FA. Phospholipid asymmetry in health and disease. Curr Opin Hematol 1998; 5: 122-31.
- 2 Arese P, Turrini F, Schwarzer E. Band 3/complement-mediated recognition and removal of normally senescent and pathological human erythrocytes. Cell Physiol Biochem 2005; 16: 133-46.
- 3 Low PS, Waugh SM, Zinke K, Drenckhahn D. The role of hemoglobin denaturation and band 3 clustering in red blood cell aging. Science 1985; 277: 531-3.
- 4 Lang SK, Roll B, Myssina S, et al. Enhanced erythrocyte apoptosis in sickle cell anemia, thalassemia and glucose-6-phosphate dehydrogenase deficiency. Cell Physiol Biochem 2002; 12: 365-72.
- 5 Lang SK, Lang AP, Bauer C, et al. Mechanisms of suicidal erythrocyte death. Cell Physiol Biochem 2005; 15: 195-202.
- 6 Mandal D, Mazumder A, Das P, Kundu M, Basu J. Fas-, caspase 8- and caspase 3-dependent signaling regulate the activity of the aminophospholipid translocase and phosphatidylserine externalization in human erythrocytes. J Biol Chem 2005; 280: 39460-7.
- 7 Murphy CS, Samuel UB, Harrison T, et al. Erythrocyte detergent-resistant membrane proteins: their characterization and selective uptake during malaria infection. Blood 2004; 103: 1920-8.
- 8 Salzer U, Prohaska R. Stomatin, flotillin-1, and flotillin-2 are the major integral proteins of erythrocyte lipid rafts. Blood 2001; 97: 1141-3.
- 9 Wang Y, Morrow S. Identification and characterization of human SLP-2, a novel homologue of stomatin (7.2b) present in erythrocytes and other tissues. J Biol Chem 2000; 275: 8062-71.
- 10 Salzer U, Hinterdorfer P, Hunger U, Borken C, Prohaska R. (Ca++)-dependent vesicle release from erythrocyte involves stomatin-specific lipid rafts, synexin (annexin VII), and sorcin. Blood 2002; 99: 2569-77.
- 11 Wolfe LC. The membrane and the lesions of storage in preserved red cells. Transfusion 1985; 25: 185-203.
- 12 Bessos H, Seghatchian J. Red cell storage lesion: the potential impact of storage-induced CD47 decline on immunomodulation and the survival of leucofiltered red cells. Transfus Apheresis Sci 2005; 32: 227-32.
- 13 Greenwalt TJ. The how and why of exocytic vesicles. Transfusion 2006; 46: 143-52.
- 14 Hovav T, Yedgar S, Manny N, Barshtein G. Alteration of red cell aggregability and shape during blood storage. Transfusion 1999; 39: 277-81.
- 15 Messana I, Ferroni L, Misiti G, et al. Blood bank conditions and RBCs: the progressive loss of metabolic modulation. Transfusion 2000; 40: 353-60.
- 16 Wagner GM, Chiu DT, Qju JH, Heath RH, Lubin BH. Spectrin oxidation correlates with membrane vasiculation in stored RBC. Blood 1987; 69: 1777-81.
- 17 Dumaswala UJ, Zhuo L, Jacobsen DW, Jain SK, Sukalski KA. Protein and lipid oxidation of banked human erythrocytes: role of glutathione. Free Rad Biol Med 1999; 27: 1041-9.
- 18 Kriebardis AG, Antonelou MH, Stamoulis KE, et al. Membrane protein carbonylation in non-leukodepleted CPDA-preserved red blood cells. Blood Cells Mol Dis 2006; 36: 279-82.
- 19 Wolfe LC. Oxidative injuries to the red cell membrane during conventional blood preservation. Semin Hematol 1989; 26: 307-12.
- 20 Solheim BG, Flesland O, Seghatchian J, Brosstad F. Clinical implications of red blood cell and platelet storage lesions: an overview. Transfus Apher Sci 2004; 31: 185-9.
- 21 Dodge JT, Mitchell C, Hanahan DJ. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes. Arch Biochem Biophys 1963; 100: 119-30.
- 22 Mueller TJ, Jackson CW, Dockter ME, Morrison M. Membrane skeletal alterations during in vivo mouse red cell aging. Increase in the band 4.1a:4.1b ratio. J Clin Invest 1987; 79: 492-9.
- 23 Antonelou MH, Papassideri IS, Karababa FJ, et al. Defective organization of the erythroid cell membrane in a novel case of congenital anemia. Blood Cells Mol Dis 2003; 30: 43-54.
- 24 Ando K, Beppu M, Kikugawa K, Hamasaki N. Increased susceptibility of stored erythrocytes to anti-band 3 IgG autoantibody binding. Biochim Biophys Acta 1993; 1178: 127-34.
- 25 Szymanski IO, Odgren PR, Valeri CR. Relationship between the third component of human complement (C3) bound to stored preserved erythrocytes and their viability in vivo. Vox Sang 1985; 49: 34-41.
- 26 Gareau R, Brisson GR, Goulet H, Dube J. Blood banking-induced senescent modifications on red blood cells. Cell Mol Biol 1992; 38: 395-8.
- 27 Ghailani N, Guillemin C, Vigneron C. Study of the vesicles released during conservation of red cells. Nour Rev Fr Hematol 1995; 37: 141-7.
- 28 Diaz C, Morkowski J, Schroit AJ. Generation of phenotypically aged phosphatidylserine-expressing erythrocytes by dilauroylphosphatidylcholine-induced vesiculation. Blood 1996; 87: 2956-61.
- 29 Dumaswala UJ, Dumaswala RU, Levin DS, Greenwalt TJ. Improved red blood cell preservation correlates with decreased loss of bands 3, 4.1, acetylcholinesterase, and lipids in microvesicles. Blood 1996; 87: 1612-16.
- 30 Greenwalt TJ, Bryan DJ, Dumaswala UJ. Erythrocyte membrane vesiculation and changes in membrane composition during storage in citrate-phosphate-dextrose-adenine-1. Vox Sang 1984; 47: 261-70.
- 31 Sparrow RL, Healey G, Patton KA, Veale MF. Red blood cell age determines the impact of storage and leukocyte burden on cell adhesion molecules, glycophorin A and the release of annexin V. Transfus Apher Sci 2006; 34: 15-23.
- 32 Samuel UB, Mohandas N, Harrison T, et al. The role of cholesterol and glycosyphosphatidylinositol-anchored proteins of erythrocyte rafts in regulating content and malarial infection. J Biol Chem 2001; 276: 29319-29.
- 33
Ciana A,
Balduini C,
Minetti G.
Detergent-resistant membranes in human erythrocytes and their connection to the membrane skeleton.
J Biosci
2005; 30: 318-28.
10.1007/BF02703727 Google Scholar
- 34 Knowles DW, Tilley L, Mohandas N, Chasis JA. Erythrocyte membrane vesiculation: model for the molecular mechanism of protein sorting. Proc Natl Acad Sci U S A 1997; 94: 12969-74.
- 35 Kiefer CR, Snyder LM. Oxidation and erythrocyte senescence. Curr Opin Hematol 2000; 7: 113-6.
- 36 Verzili D, Zamparelli C, Mattei B, Noegel AA, Chiancone E. The sorcin-annexin VII calcium–dependent interaction requires the sorcin N-terminal domain. FEBS 2000; 471: 197-200.
- 37 Frabetti F, Musiani D, Marini M, et al. White cell apoptosis in packed red cells. Transfusion 1998; 38: 1082-9.
- 38 Snyder EL, Kuter DJ. Apoptosis in transfusion medicine: of death and dying—is that all there is? Transfusion 2000; 40: 135-8.
- 39 Berg CP, Engels IH, Rothbart A, et al. Human mature red blood cells express caspase-3 and caspace-8, but are devoid of mitochondrial regulators of apoptosis. Cell Death Differ 2001; 8: 1197-206.
- 40 Mandal D, Moitra KP, Saha S, Basu J. Caspase 3 regulates phosphatidylserine externalization and phagocytosis of oxidatively stressed erythrocytes. FEBS Lett 2002; 513: 184-8.
- 41 Mandal D, Baudin-Creuza V, Bhattacharyya A, et al. Caspase 3-mediated proteolysis of the N-terminal cytoplasmic domain of the human erythroid anion exchanger 1 (Band 3). J Biol Chem 2003; 278: 52551-8.
- 42 Geldwerth D, Kuypers FA, Bütikofer P, et al. Transbilayer mobility and distribution of red cell phospholipids during storage. J Clin Invest 1993; 92: 308-14.
- 43 Ghio M, Contini P, Mazzei C, et al. Soluble HLA class I, HLA class II and Fas ligand in blood components: a possible key to explain the immunomodulatory effects of allogeneic blood transfusions. Blood 1999; 93: 1770-7.