Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen

Blood

Volumn 120, Issue 2, 2012, Pages 424-430

  Safeukui, Innocent ^a,b,g   Buffet, Pierre A ^c,d   Deplaine, Guillaume ^a,b,c   Perrot, Sylvie ^a,b   Brousse, Valentine ^e   Ndour, Alioune ^c,d   Nguyen, Marie ^a   Mercereau Puijalon, Odile ^a,b   David, Peter H ^a,b   Milon, Geneviève ^a   Mohandas, Narla ^f  

^a INSTITUT PASTEUR   (France)

^b CNRS   (France)

^c INSERM   (France)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

^f NEW YORK BLOOD CENTER   (United States)

^g UNIVERSITY OF NOTRE DAME   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LYSOPHOSPHATIDYLCHOLINE;

ARTICLE; ERYTHROCYTE LIFESPAN; EX VIVO STUDY; HUMAN; HUMAN CELL; HUMAN TISSUE; OSMOSIS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SPLEEN;

EID: 84864032271     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2012-01-404103     Document Type: Article

References (38)

1. Chen L, Weiss L. The role of the sinus wall in the passage of erythrocytes through the spleen. Blood. 1973;41(4):529-537.
2. Larsen F, Katz S, Roufogalis B, Brooks D. Physiological shear stresses enhance the Ca2+ permeability of human erythrocytes. Nature. 1981; 294(5842):667-668. (Pubitemid 12213970)
3. Hebbel RP, Mohandas N. Reversible deformation-dependent erythrocyte cation leak. Extreme sensitivity conferred by minimal peroxidation. Biophys J. 1991;60(3):712-715.
4. Johnson RM. Membrane stress increases cation permeability in red cells. Biophys J. 1994;67(5): 1876-1881. (Pubitemid 24342058)
5. Dyrda A, Cytlak U, Ciuraszkiewicz A, et al. Local membrane deformations activate Ca2+-dependent K+ and anionic currents in intact human red blood cells. PLoS One. 2010;5(2):e9447.
6. Mohandas N, Clark MR, Jacobs MS, Shohet SB. Analysis of factors regulating erythrocyte deformability. J Clin Invest. 1980;66(3):563-573. (Pubitemid 10053921)
7. Clark MR, Mohandas N, Shohet SB. Osmotic gradient ektacytometry: comprehensive characterization of red cell volume. Blood. 1983;61(5):899-910. (Pubitemid 13089589)
8. Murdock RC, Reynolds C, Sarelius IH, Waugh RE. Adaptation and survival of surface-deprived red blood cells in mice. Am J Physiol Cell Physiol. 2000;279(4):C970-C980.
9. Griggs R,Weisman RJr., Harris J. Alterations in osmotic and mechanical fragility related to in vivo erythrocyte aging and splenic sequestration in hereditary spherocytosis. J Clin Invest. 1960;39:89-101.
10. Reliene R, Mariani M, Zanella A, et al. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis. Blood. 2002;100(6):2208-2215. (Pubitemid 35001258)
11. Perrotta S, Gallagher PG, Mohandas N. Hereditary spherocytosis. Lancet. 2008;372(9647): 1411-1426.
12. Young LE. Observations on inheritance and heterogeneity of chronic spherocytosis. Trans Assoc Am Physicians. 1955;68:141-148.
13. Becker PS, Lux SE. Hereditary spherocytosis and related disorders. Clin Haematol. 1985;14(1):15-43.
14. Jacob HS, Jandl JH. Increased cell membrane permeability in the pathogenesis of hereditary spherocytosis. J Clin Invest. 1964;43:1704-1720.
15. Palek J, Sahr KE. Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect. Blood. 1992;80(2):308-330.
16. Buesing KL, Tracy ET, Kiernan C, et al. Partial splenectomy for hereditary spherocytosis: a multi-institutional review. J Pediatr Surg. 2011; 46(1):178-183.
17. Jandl JH, Greenberg MS, Yonemoto RH, Castle WB. Clinical determination of the sites of red cell sequestration in hemolytic anemias. J Clin Invest. 1956;35(8):842-867.
18. Schloesser Ll Korst D, Clatanoff DV, Schilling RF. Radioactivity over the spleen and liver following the transfusion of chromium51-labelled erythrocytes in hemolytic anemia. J Clin Invest. 1957; 36(10):1470-1485.
19. Wiley JS. Red cell survival studies in hereditary spherocytosis. J Clin Invest. 1970;49(4):666-672.
20. Buffet PA, Milon G, Brousse V, et al. Ex vivo perfusion of human spleens maintains clearing and processing functions. Blood. 2006;107(9):3745-3752.
21. Mohandas N, Greenquist A, Shohet S. Bilayer balance and regulation of red cell shape changes. J Supramol Struct. 1978;9(3):453-458.
22. Lange Y, Slayton J. Interaction of cholesterol and lysophosphatidylcholine in determining red cell shape. J Lipid Res. 1982;23(8):1121-1127. (Pubitemid 13187607)
23. Chasis JA, Schrier SL. Membrane deformability and the capacity for shape change in the erythrocyte. Blood. 1989;74(7):2562-2568. (Pubitemid 19286480)
24. Khodadad JK, Waugh RE, Podolski JL, Josephs R, Steck TL. Remodeling the shape of the skeleton in the intact red cell. Biophys J. 1996;70(2): 1036-1044. (Pubitemid 26028319)
25. Safeukui I, Correas JM, Brousse V, et al. Retention of Plasmodium falciparum ring-infected erythrocytes in the slow, open microcirculation of the human spleen. Blood. 2008;112(6):2520-2528.
26. Deplaine G, Safeukui I, Jeddi F, et al. The sensing of poorly deformable red blood cells by the human spleen can be mimicked in vitro. Blood. 2011;117(8):e88-e95.
27. Hardeman MR, Ince C. Clinical potential of in vitro measured red cell deformability, a myth? Clin Hemorheol Microcirc. 1999;21(3-4):277-284. (Pubitemid 30130904)
28. Beum PV, Lindorfer MA, Hall BE, et al. Quantitative analysis of protein co-localization on B cells opsonized with rituximab and complement using the ImageStream multispectral imaging flow cytometer. J Immunol Methods. 2006;317(1-2):90-99. (Pubitemid 44809210)
29. Parpart AKLP, Parpart ER, Gregg JR, Chase AM. The osmotic resistance (fragility) of human red cells. J Clin Invest. 1947;26(4):636-640.
30. Cooper RA, Jandl JH. Bile salts and cholesterol in the pathogenesis of target cells in obstructive jaundice. J Clin Invest. 1968;47(4):809-822.
31. Cooper RA, Jandl JH. The role of membrane lipids in the survival of red cells in hereditary spherocytosis. J Clin Invest. 1969;48(4):736-744.
32. Johnson RM, Gannon SA. Erythrocyte cation permeability induced by mechanical stress: a model for sickle cell cation loss. Am J Physiol. 1990; 259(5 Pt 1):C746-C751. (Pubitemid 20385676)
33. Ney PA, Christopher MM, Hebbel RP. Synergistic effects of oxidation and deformation on erythrocyte monovalent cation leak. Blood. 1990;75(5): 1192-1198. (Pubitemid 20086829)
34. Johnson RM, Tang K. Induction of a Ca2+-activated K+ channel in human erythrocytes by mechanical stress. Biochim Biophys Acta. 1992;1107(2): 314-318.
35. Bertles JF. Sodium transport across the surface membrane of red blood cells in hereditary spherocytosis. J Clin Invest. 1957;36(6 Pt 1):816-824.
36. Jacob H, Macdonald R, Jandl J. Regulation of spleen growth and sequestering function. J Clin Invest. 1963;42:1476-1490.
37. Waugh R, Sarelius I. Effects of lost surface area on red blood cells and red blood cell survival in mice. Am J Physiol. 1996;271(6 Pt 1):C1847-C1852.
38. Groom A, Schmidt E, MacDonald I. Microcirculatory pathways and blood flow in spleen: new insights from washout kinetics, corrosion casts, and quantitative intravital videomicroscopy. Scanning Microsc. 1991;5(1):159-173.