Adhesive receptors on malaria-parasitized red cells

Bailliere's Best Practice and Research in Clinical Haematology

Volumn 12, Issue 4, 1999, Pages 747-761

  Baruch, Dror I ^a  

^a NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

Author keywords

Antigenic variation; Cytoadhesion; Erythrocyte; Malaria; PfEMPI; Plasmodium falciparum; Var genes

Indexed keywords

ANTIGENIC VARIATION; CELL ADHESION; ERYTHROCYTE; HOST PARASITE INTERACTION; MULTIGENE FAMILY; PARASITE VIRULENCE; PATHOGENESIS; PLASMODIUM FALCIPARUM; PRIORITY JOURNAL; PROTEIN FAMILY; REVIEW;

EID: 0033506526     PISSN: 15216926     EISSN: None     Source Type: Journal    
DOI: 10.1053/beha.1999.0051     Document Type: Article

References (89)

1. Marsh K, Snow R W. Host-parasite interaction and morbidity in malaria endemic areas. Philosophical Transactions of the Royal Society of London Series B, Biological Sciences. 352:1997;1385-1394.
2. Snow R W, Marsh K. The epidemiology of clinical malaria among African children. Bulletin de l' Institut Pasteur. 96:1998;15-23.
3. Berendt A R, Ferguson D J, Gardner J. Molecular mechanisms of sequestration in malaria. Parasitology. 108:1994;S19-S28.
4. Wahlgren M, Fernandez V, Scholander C. Rosetting. Parasitology Today. 10:1994;73-79.
5. Baruch D I, Pasloske B L, Singh H B. Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes. Cell. 82:1995;77-87.
6. Baruch D I, Gormley J A, Ma C. Plasmodium falciparum erythrocyte membrane protein 1 is a parasitized erythrocyte receptor for adherence to CD36, thrombospondin, and intercellular adhesion molecule 1. Proceedings of the National Academy of Sciences of the USA. 93:1996;3497-3502.
7. Howard R J, Gilladoga A D. Molecular studies related to the pathogenesis of cerebral malaria. Blood. 74:1989;2603-2618.
8. Rowe J A, Moulds J M, Newbold C I. P. falciparum rosetting mediated by a parasite-variant erythrocyte membrane protein and complement-receptor 1. Nature, London. 388:1997;292-295.
9. Deitsch K W, Moxon E R, Wellems T E. Shared themes of antigenic variation and virulence in bacterial, protozoal, and fungal infections. Microbiology and Molecular Biology Reviews. 61:1997;281-293.
10. Berendt A R, Ferguson D JP, Newbold C I. Sequestration in plasmodium falciparum malaria: sticky cells and sticky problems. Parasitology Today. 6:1990;247-254.
11. Handunnetti S M, Mendis K N, David P H. Antigenic variation of cloned Plasmodium fragile in its natural host Macaca sinica. Sequential appearance of successive variant antigenic types. Journal of Experimental Medicine. 165:1987;1269-1283.
12. Allred D R. Antigenic variation in Babesia bovis: how similar is it to that in Plasmodium falciparum ? Annals of Tropical Medicine and Parasitology. 92:1998;461-472.
13. McLean S A, Pearson C D, Phillips R S. Antigenic variation in Plasmodium chabaudi: analysis of parent and variant populations by cloning. Parasite Immunology. 8:1986;415-424.
14. Brown K N, Brown I N. Immunity to malaria: antigenic variation in chronic infections of Plasmodium knowlesi. Nature, London. 208:1965;1286-1288.
15. Barnwell J W, Howard R J, Coon H A. Splenic requirement for antigenic variation and expression of the variant antigen on the erythrocyte membrane in clonedPlasmodium knowlesi. Infection and Immunity. 40:1983;985-994.
16. Leech J H, Barnwell J W, Miller L H. Identification of a strain-specific malarial antigen exposed on the surface of Plasmodium falciparum -infected erythrocytes. Journal of Experimental Medicine. 159:1984;1567-1575.
17. Smith J D, Chitnis C E, Craig A G. Switches in expression of Plasmodium falciparum var genes correlate with changes in antigenic and cytoadherence phenotypes of infected erythrocytes. Cell. 82:1995;101-110.
18. Su X Z, Heatwole V M, Wertheimer S P. The large diverse gene family var encodes proteins involved in cytoadherence and antigenic variation of Plasmodium falciparum -infected erythrocytes. Cell. 82:1995;89-100.
19. Hommel M, David P H, Oligino L D. Surface alterations of erythrocytes in Plasmodium falciparum malaria. Journal of Experimental Medicine. 157:1983;1137-1148.
20. Howard R J, Barnwell J W, Rock E P. Two approximately 300 kilodalton Plasmodium falciparum proteins at the surface membrane of infected erythrocytes. Molecular and Biochemical Parasitology. 27:1988;207-223.
21. Marsh K, Howard R J. Antigens induced on erythrocytes by P. falciparum: expression of diverse and conserved determinants. Science. 231:1986;150-153.
22. Bull P C, Lowe B S, Kortok M. Parasite antigens on the infected red cell surface are targets for naturally acquired immunity to malaria. Nature Medicine. 4:1998;358-360.
23. Roberts D J, Craig A G, Berendt A R. Rapid switching to multiple antigenic and adhesive phenotypes in malaria. Nature, London. 357:1992;689-692.
24. Brannan L R, Turner C M, Phillips R S. Malaria parasites undergo antigenic variation at high rates in vivo. Philosophical Transactions of the Royal Society of London Series B, Biological Sciences. 256:1994;71-75.
25. Snow R W, Marsh K. New insights into the epidemiology of malaria relevant for disease control. British Medical Bulletin. 54:1998;293-309.
26. Aguiar J C, Albrecht G R, Cegielski P. Agglutination of Plasmodium falciparum -infected erythrocytes from East and West Africa isolates by human sera from distant geographic regions. American Journal of Tropical Medicine and Hygiene. 47:1992;621-632.
27. Newbold C I, Pinches R, Roberts D J. Plasmodium falciparum: the human agglutinating antibody response to the infected red cell surface is predominantly variant specific. Experimental Parasitology. 75:1992;281-292.
28. Magowan C, Wollish W, Anderson L. Cytoadherence by Plasmodium falciparum -infected erythrocytes is correlated with the expression of a family of variable proteins on infected erythrocytes. Journal of Experimental Medicine. 168:1988;1307-1320.
29. Udeinya I J, Miller L H, McGregor I A. Plasmodium falciparum strain-specific antibody blocks binding of infected erythrocytes to amelanotic melanoma cells. Nature, London. 303:1983;429-431.
30. Baruch D I, Ma X C, Singh H B. Identification of a region of PfEMP1 that mediates adherence of Plasmodium falciparum infected erythrocytes to CD36: conserved function with variant sequence. Blood. 90:1997;3766-3775.
31. Chaiyaroj S C, Angkasekwinai P, Buranakiti A. Cytoadherence characteristics of Plasmodium falciparum isolates from Thailand: evidence for chondroitin sulfate A as a cytoadherence receptor. American Journal of Tropical Medicine and Hygiene. 55:1996;76-80.
32. Newbold C, Warn P, Black G. Receptor-specific adhesion and clinical-disease in Plasmodium falciparum. American Journal of Tropical Medicine and Hygiene. 57:1997;389-398.
33. Reeder J C, Rogerson S J, al-Yaman F. Diversity of agglutinating phenotype, cytoadherence, and rosette-forming characteristics of Plasmodium falciparum isolates from Papua New Guinean children. American Journal of Tropical Medicine and Hygiene. 51:1994;45-55.
34. Rowe A, Obeiro J, Newbold C I. Plasmodium falciparum rosetting is associated with malaria severity in Kenya. Infection and Immunity. 63:1995;2323-2326.
35. Miller L H. Distribution of mature trophozoites and schizonts of Plasmodium falciparum in the organs of Aotus trivergatus, the night monkey. American Journal of Tropical Medicine and Hygiene. 18:1969;860-865.
36. Bignami A, Bastianeli G. Observations of estivo-autumnal malaria. Reforma Medica. 6:1889;1334-1335.
37. MacPherson G G, Warrell M J, White N J. Human cerebral malaria. A quantitative ultrastructural analysis of parasitized erythrocyte sequestration. American Journal of Pathology. 119:1985;385-401.
38. Fried M, Duffy P E. Maternal malaria and parasite adhesion. Journal of Molecular Medicine. 76:1998;162-171.
39. Fried M, Duffy P E. Adherence of Plasmodium falciparum to chondroitin sulfate A in the human placenta. Science. 272:1996;1502-1504.
40. Udeinya I J, Graves P M, Carter R. Plasmodium falciparum: effect of time in continuous culture on binding to human endothelial cells and amelanotic melanoma cells. Experimental Parasitology. 56:1983;207-214.
41. David P H, Hommel M, Miller L H. Parasite sequestration in Plasmodium falciparum malaria: spleen and antibody modulation of cytoadherence of infected erythrocytes. Proceedings of the National Academy of Sciences of the USA. 80:1983;5075-5076.
42. Langreth S G, Peterson E. Pathogenicity, stability and immunogenicity of a knobless clone of Plasmodium falciparum in Colombian owl monkeys. Infection and Immunity. 47:1985;760-766.
43. Hayward R E, Tiwari B, Piper K P. Virulence and transmission success of the malarial parasite Plasmodium falciparum. Proceedings of the National Academy of Sciences of the USA. 96:1999;4563-4568.
44. Silamut K, Phu N H, Whitty C. A quantitative analysis of the microvascular sequestration of malaria parasites in the human brain. American Journal of Pathology. 155:1999;395-410.
45. Aley S B, Sherwood J A, Howard R J. Knob-positive and knob-negative Plasmodium falciparum differ in expression of a strain-specific malarial antigen on the surface of infected erythrocytes. Journal of Experimental Medicine. 160:1984;1585-1590.
46. Leech J H, Barnwell J W, Aikawa M. Plasmodium falciparum malaria: association of knobs on the surface of infected erythrocytes with a histidine-rich protein and the erythrocyte skeleton. Journal of Cell Biology. 98:1984;1256-1264.
47. Sharma Y D. Knob proteins in falciparum malaria. Indian Journal of Medical Research. 106:1997;53-62.
48. Waller K L, Cooke B M, Nunomura W. Mapping the binding domains involved in the interaction between the Plasmodium falciparum knob-associated histidine-rich protein (KAHRP) and the cytoadherence ligand P. falciparum erythrocyte membrane protein 1 (PfEMP1). Journal of Biological Chemistry. 274:1999;23808-23813.
49. Hernandez-Rivas R, Mattei D, Sterkers Y. Expressed var genes are found in Plasmodium falciparum subtelomeric regions. Molecular and Cellular Biology. 17:1997;604-611.
50. Deitsch K W, del Pinal A, Wellems T E. Intra-cluster recombination and var transcription switches in the antigenic variation of Plasmodium falciparum. Molecular and Biochemical Parasitology. 101:1999;107-116.
51. Scherf A, Hernandez-Rivas R, Buffet P. Antigenic variation in malaria: in situ switching, relaxed and mutually exclusive transcription of var genes during intra-erythrocytic development in Plasmodium falciparum. European Molecular Biology Organization Journal. 17:1998;5418-5426.
52. Chen Q, Fernandez V, Sundstrom A. Developmental selection of var gene expression in Plasmodium falciparum. Nature, London. 394:1998;392-395.
53. Biggs B A, Anders R F, Dillon H E. Adherence of infected erythrocytes to venular endothelium selects for antigenic variants of Plasmodium falciparum. Journal of Immunology. 149:1992;2047-2054.
54. Ockenhouse C F, Tegoshi T, Maeno Y. Human vascular endothelial cell adhesion receptors for Plasmodium falciparum -infected erythrocytes: roles for endothelial leukocyte adhesion molecule 1 and vascular cell adhesion molecule 1. Journal of Experimental Medicine. 176:1992;1183-1189.
55. Sherman I W, Crandall I E, Guthrie N. The sticky secrets of sequestration. Parasitology Today. 11:1995;378-384.
56. Treutiger C J, Heddini A, Fernandez V. PECAM-1/CD31, an endothelial receptor for binding Plasmodium falciparum -infected erythrocytes. Nature Medicine. 3:1997;1315-1316.
57. Ho M, Schollaardt T, Niu X F. Characterization of Plasmodium falciparum -infected erythrocyte and P-selectin interaction under flow conditions. Blood. 91:1998;4803-4809.
58. Ho M, White N J. Molecular mechanisms of cytoadherence in malaria. American Journal of Physiology, Cell Physiology. 45:1999;C1231-C1242.
59. Turner G D, Morrison H, Jones M. An immunohistochemical study of the pathology of fatal malaria. Evidence for widespread endothelial activation and a potential role for intercellular adhesion molecule-1 in cerebral sequestration. American Journal of Pathology. 145:1994;1057-1069.
60. Ockenhouse C F, Ho M, Tandon N N. Molecular basis of sequestration in severe and uncomplicated Plasmodium falciparum malaria: differential adhesion of infected erythrocytes to CD36 and ICAM-1. Journal of Infectious Diseases. 164:1991;163-169.
61. Hasler T, Handunnetti S M, Aguiar J C. In vitro rosetting, cytoadherence, and microagglutination properties of Plasmodium flaciparum -infected erythrocytes from Gambian and Tanzanian patients. Blood. 76:1990;1845-1852.
62. Udomsangpetch R, Taylor B J, Looareesuwan S. Receptor specificity of clinical Plasmodium falciparum isolates: nonadherence to cell-bound E-selectin and vascular cell adhesion molecule-1. Blood. 88:1996;2754-2760.
63. Rogerson S J, Chaiyaroj S C, Ng K. Chondroitin sulfate A is a cell surface receptor for Plasmodium falciparum -infected erythrocytes. Journal of Experimental Medicine. 182:1995;15-20.
64. Daviet L, McGregor J L. Vascular biology of CD36: roles of this new adhesion molecule family in different disease states. Thrombosis and Haemostasis. 78:1997;65-69.
65. Baruch D I, Ma X C, Pasloske B. CD36 peptides that block cytoadherence define the CD36 binding region for Plasmodium falciparum infected erythrocytes. Blood. 94:1999;2121-2127.
66. Adams J C. Thrombospondin-1. International Journal of Biochemistry and Cell Biology. 29:1997;861-865.
67. Bella J, Kolatkar P R, Marlor C W. The structure of the two amino-terminal domains of human ICAM-1 suggests how it functions as a rhinovirus receptor and as an LFA-1 integrin ligand. Proceedings of the National Academy of Sciences of the USA. 95:1998;4140-4145.
68. Wang J, Springer T A. Structural specializations of immunoglobulin superfamily members for adhesion to integrins and viruses. Immunology Reviews. 163:1998;197-215.
69. Ockenhouse C F, Betageri R, Springer T A. Plasmodium falciparum -infected erythrocytes bind ICAM-1 at a site distinct from LFA-1, Mac-1, and human rhinovirus. Cell. 68:1992;63-69.
70. Rogerson S J, Novakovic S, Cooke B M. Plasmodium falciparum -infected erythrocytes adhere to the proteoglycan thrombomodulin in static and flow-based systems. Experimental Parasitology. 86:1997;8-18.
71. Udomsangpetch R, Reinhardt P H, Schollaardt T. Promiscuity of clinical Plasmodium falciparum isolates for multiple adhesion molecules under flow conditions. Journal of Immunology. 158:1997;4358-4364.
72. Scholander C, Treutiger C J, Hultenby K. Novel fibrillar structure confers adhesive property to malaria-infected erythrocytes. Nature Medicine. 2:1996;204-208.
73. Barragan A, Spillman D, Kremsner P G. Plasmodium falciparum: molecular background to strain-specific rosette disruption by glycosaminoglycans and sulfated glycoconjugates. Experimental Parasitology. 91:1999;133-143.
74. Chen Q, Barragan A, Fernandez V. Identification of Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) as the rosetting ligand of the malaria parasite P. falciparum. Journal of Experimental Medicine. 187:1998;15-23.
75. Rowe A, Berendt A R, Marsh K. Plasmodium falciparum: a family of sulfated glycoconjugates disrupts erythrocyte rosettes. Experimental Parasitology. 79:1994;506-516.
76. Smith J D, Kyes S, Craig A G. Analysis of adhesive domains from the A4VAR Plasmodium falciparum erythrocyte membrane protein-1 identifies a CD36 binding domain. Molecular and Biochemical Parasitology. 97:1998;133-148.
77. Buffet P, Gamain B, Scheidig C. P. falciparum domain mediating adhesion to chondroitin sulfate A: a receptor for human placental infection. Proceedings of the National Academy of Sciences of the USA. 96:1999;12 743-12 748.
78. Cooke B M, Nicoll C L, Baruch D. A recombinant peptide based on PfEMP-1 blocks and reverses adhesion of malaria-infected red blood cells to CD36 under flow. Molecular Microbiology. 30:1998;83-90.
79. Chaiyaroj S C, Coppel R L, Novakovic S. Multiple ligands for cytoadherence can be present simultaneously on the surface of Plasmodium falciparum -infected erythrocytes. Proceedings of the National Academy of Sciences of the USA. 91:1994;10805-10808.
80. Reeder J C, Cowman A F, Davern K M. The adhesion of Plasmodium falciparum -infected erythrocytes to chondroitin sulfate A is mediated by P. falciparum erythrocyte membrane protein 1. Proceedings of the National Academy of Sciences of the USA. 96:1999;5198-5202.
81. Gardner J P, Pinches R A, Roberts D J. Variant antigens and endothelial receptor adhesion in plasmodium falciparum. Proceedings of the National Academy of Sciences of the USA. 93:1996;3503-3508.
82. Smith, J, D, Craig, A, G, Kriek, N, Identification of a Plasmodium falciparum ICAM-1 binding domain; a parasite adhesion trait implicated in the lethal malaria disease complication cerebral malaria, Proceedings of the National Academy of Sciences of the USA.
83. Cooke B M, Coppel R L. Cytoadhesion and falciparum malaria: going with the flow. Parasitology Today. 11:1995;282-287.
84. Cooke B M, Rogerson S J, Brown G V. Adhesion of malaria-infected red blood cells to chondroitin sulfate A under flow conditions. Blood. 88:1996;4040-4044.
85. Cooke B M, Berendt A R, Craig A G. Rolling and stationary cytoadhesion of red blood cells parasitized by Plasmodium falciparum: separate roles for ICAM-1, CD36 and thrombospondin. British Journal of Haematology. 87:1994;162-170.
86. McCormick C J, Craig A, Roberts D. Intercellular adhesion molecule-1 and CD36 synergize to mediate adherence of Plasmodium falciparum -infected erythrocytes to cultured human microvascular endothelial cells. Journal of Clinical Investigation. 100:1997;2521-2529.
87. Siano J P, Grady K K, Millet P. Plasmodium falciparum - soluble thrombospondin increases cytoadherence of parasitized erythrocytes to human microvascular endothelium under shear-flow conditions. Experimental Parasitology. 87:1997;69-72.
88. Crabb B S, Cooke B M, Reeder J C. Targeted gene disruption shows that knobs enable malaria-infected red cells to cytoadhere under physiological shear stress. Cell. 89:1997;287-296.
89. Udeinya I J, Akogyeram C O. Induction of adhesiveness in human endothelial cells by Plasmodium falciparum -infected erythrocytes. American Journal of Tropical Medicine and Hygiene. 48:1993;488-495.