Surface Area Loss and Increased Sphericity Account for the Splenic Entrapment of Subpopulations of Plasmodium falciparum Ring-Infected Erythrocytes

PLoS ONE

Volumn 8, Issue 3, 2013, Pages

  Safeukui, Innocent ^a,b,c   Buffet, Pierre A ^d,e   Perrot, Sylvie ^a,b   Sauvanet, Alain ^f   Aussilhou, Beatrice ^f   Dokmak, Safi ^f   Couvelard, Anne ^f   Hatem, Dominique Cazals ^f   Mohandas, Narla ^g   David, Peter H ^a,b   Mercereau Puijalon, Odile ^a,b   Milon, Geneviève ^a  

^a INSTITUT PASTEUR   (France)

^b CNRS   (France)

^c UNIVERSITY OF NOTRE DAME   (United States)

^d SORBONNE UNIVERSITÉ   (France)

^e PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^f BEAUJON HOSPITAL   (France)

^g NEW YORK BLOOD CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LYSOPHOSPHATIDYLCHOLINE;

ADJUVANT THERAPY; ANALYTICAL EQUIPMENT; ARTICLE; CELL FRACTIONATION; CELL KINETICS; CELL MEMBRANE; CELL SUBPOPULATION; CELL SURFACE; COCULTURE; COMPUTER PROGRAM; CONCENTRATION LOSS; CONTROLLED STUDY; DISEASE SEVERITY; ERYTHROCYTE STRUCTURE; EX VIVO STUDY; HOST PARASITE INTERACTION; HUMAN; HUMAN CELL; NONHUMAN; OSMOTIC FRAGILITY; PARASITE LOAD; PLASMODIUM FALCIPARUM; RISK FACTOR; SPLEEN; SPLEEN FUNCTION; TROPHOZOITE;

CELL SHAPE; CELLS, CULTURED; ERYTHROCYTES; HUMANS; LYSOPHOSPHATIDYLCHOLINES; PLASMODIUM FALCIPARUM; SPLEEN;

PLASMODIUM FALCIPARUM;

EID: 84875487630     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0060150     Document Type: Article

References (32)

1. Safeukui I, Correas JM, Brousse V, Hirt D, Deplaine G, et al. (2008) Retention of Plasmodium falciparum ring-infected erythrocytes in the slow, open microcirculation of the human spleen. Blood 112: 2520-2528.
2. Chen L, Weiss L, (1972) Electron microscopy of the red pulp of human spleen. Am J Anat 134: 425-457.
3. Chen L, Weiss L, (1973) The role of the sinus wall in the passage of erythrocytes through the spleen. Blood 41: 529-537.
4. Groom A, Schmidt E, MacDonald I, (1991) Microcirculatory pathways and blood flow in spleen: new insights from washout kinetics, corrosion casts, and quantitative intravital videomicroscopy. Scanning Microsc 5: 159-173.
5. Deplaine G, Safeukui I, Jeddi F, Lacoste F, Brousse V, et al. (2011) The sensing of poorly deformable red blood cells by the human spleen can be mimicked in vitro. Blood 117: e88-95.
6. Mohandas N, Clark MR, Jacobs MS, Shohet SB, (1980) Analysis of factors regulating erythrocyte deformability. J Clin Invest 66: 563-573.
7. Clark MR, Mohandas N, Shohet SB, (1983) Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance. Blood 61: 899-910.
8. Safeukui I, Buffet P, Deplaine G, Perrot S, Brousse V, et al. (2012) Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen. Blood 120: 424-430.
9. Nash G, O' Brien E, Gordon-Smith E, Dormandy J, (1989) Abnormalities in the mechanical properties of red blood cells caused by Plasmodium falciparum. Blood 74: 855-861.
10. Herricks T, Antia M, Rathod P, (2009) Deformability limits of Plasmodium falciparum-infected red blood cells. Cell Microbiol 11: 1340-1353.
11. Esposito A, Choimet J, Skepper J, Mauritz J, Lew V, et al. (2010) Quantitative imaging of human red blood cells infected with Plasmodium falciparum. Biophys J 99: 953-960.
12. Mohandas N, Greenquist A, Shohet S, (1978) Bilayer balance and regulation of red cell shape changes. J Supramol Struct 9: 453-458.
13. Lange Y, Slayton J, (1982) Interaction of cholesterol and lysophosphatidylcholine in determining red cell shape. J Lipid Res 23: 1121-1127.
14. Murdock RC, Reynolds C, Sarelius IH, Waugh RE, (2000) Adaptation and survival of surface-deprived red blood cells in mice. Am J Physiol Cell Physiol 279: C970-980.
15. Chasis JA, Schrier SL, (1989) Membrane deformability and the capacity for shape change in the erythrocyte. Blood 74: 2562-2568.
16. Canham P, (1969) Difference in geometry of young and old human erythrocytes explained by a filtering mechanism. Circ Res 25: 39-45.
17. Herricks T, Seydel KB, Molyneux M, Taylor T, Rathod PK, (2012) Estimating physical splenic filtration of Plasmodium falciparum-infected red blood cells in malaria patients. Cell Microbiol 14: 1880-91.
18. Nash G, Linderkamp O, Pfafferroth C, Meiselman H (1988) Changes in human red cell mechanics during in vivo aging: Possible influence on removal of senescent cells. Berlin Heidelberg: Springer-Verlag 99-112 p.
19. Ogembo J, Milner D Jr, Mansfield K, Rodig S, Murphy G, et al. (2012) SIRPalpha/CD172a and FHOD1 are unique markers of littoral cells, a recently evolved major cell population of red pulp of human spleen. J Immunol 188: 4496-4505.
20. Cooper RA, Jandl JH, (1968) Bile salts and cholesterol in the pathogenesis of target cells in obstructive jaundice. J Clin Invest 47: 809-822.
21. Jacob HS, Jandl JH, (1964) Increased Cell Membrane Permeability in the Pathogenesis of Hereditary Spherocytosis. J Clin Invest 43: 1704-1720.
22. Hebbel RP, Mohandas N, (1991) Reversible deformation-dependent erythrocyte cation leak. Extreme sensitivity conferred by minimal peroxidation. Biophys J 60: 712-715.
23. Waugh R, Sarelius I, (1996) Effects of lost surface area on red blood cells and red blood cell survival in mice. Am J Physiol 271: C1847-1852.
24. Dyrda A, Cytlak U, Ciuraszkiewicz A, Lipinska A, Cueff A, et al. (2010) Local membrane deformations activate Ca2+-dependent K+ and anionic currents in intact human red blood cells. PLoS One 5: e9447.
25. Cortes A, Carret C, Kaneko O, Yim Lim BY, Ivens A, et al. (2007) Epigenetic silencing of Plasmodium falciparum genes linked to erythrocyte invasion. PLoS Pathog 3: e107.
26. Riglar DT, Richard D, Wilson DW, Boyle MJ, Dekiwadia C, et al. (2011) Super-resolution dissection of coordinated events during malaria parasite invasion of the human erythrocyte. Cell Host Microbe 9: 9-20.
27. Cortes A, (2008) Switching Plasmodium falciparum genes on and off for erythrocyte invasion. Trends Parasitol 24: 517-524.
28. Silva M, Cooke B, Guillotte M, Buckingham D, Sauzet J, et al. (2005) A role for the Plasmodium falciparum RESA protein in resistance against heat shock demonstrated using gene disruption. Mol Microbiol 56: 990-1003.
29. Mills J, Diez-Silva M, Quinn D, Dao M, Lang M, et al. (2007) Effect of plasmodial RESA protein on deformability of human red blood cells harboring Plasmodium falciparum. Proc Natl Acad Sci U S A 104: 9213-9217.
30. Pouvelle B, Buffet P, Lepolard C, Scherf A, Gysin J, (2000) Cytoadhesion of Plasmodium falciparum ring-stage-infected erythrocytes. Nat Med 6: 1264-1268.
31. Hardeman MR, Ince C, (1999) Clinical potential of in vitro measured red cell deformability, a myth? Clin Hemorheol Microcirc 21: 277-284.
32. Parpart AK, Lorenz PB, Parpart ER, Gregg JR, Chase AM, (1947) The osmotic resistance (fragility) of human red cells. J Clin Invest 26: 636-640.