Sickle erythrocyte adherence to endothelium at low shear: Role of shear stress in propagation of vaso-occlusion

American Journal of Hematology

Volumn 70, Issue 3, 2002, Pages 216-227

  Montes, Richard A O ^a   Eckman, James R ^b,d   Hsu, Lewis L ^c,d   Wick, Timothy M ^a  

^a Georgia Institute of Technology   (United States)

^b EMORY UNIVERSITY   (United States)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d Georgia Compreh Sickle Cell Center   (United States)

Author keywords

Endothelial cell adhesion; Microvascular blood flow; Sickle cell adhesion; Sickle cell anemia

Indexed keywords

ARTICLE; BLOOD FLOW VELOCITY; BLOOD VESSEL OCCLUSION; ENDOTHELIUM CELL; ERYTHROCYTE ADHESIVENESS; HUMAN; HUMAN CELL; MATHEMATICAL MODEL; MICROCIRCULATION; MICROVASCULATURE; MOLECULAR INTERACTION; PRIORITY JOURNAL; RECEPTOR AFFINITY; SHEAR STRESS; SICKLE CELL ANEMIA; TISSUE INJURY; VENULE;

ANEMIA, SICKLE CELL; CAPILLARIES; CELL ADHESION; CELLS, CULTURED; ENDOTHELIUM, VASCULAR; ERYTHROCYTES, ABNORMAL; HEMORHEOLOGY; HUMANS; MATHEMATICS; MODELS, BIOLOGICAL; THROMBOSPONDINS; TUMOR NECROSIS FACTOR-ALPHA; VASCULAR CELL ADHESION MOLECULE-1; VASCULAR DISEASES; VENULES;

EID: 0036083026     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.10145     Document Type: Article

References (65)

1. Erythrocyte adherence to endothelium in sickle-cell anemia: A possible determinant of disease severity
2. Adhesion of normal and sickle erythrocytes to endothelial monolayer cultures
3. Blockade of adhesion of sickle cells to endothelium by monoclonal antibodies
4. Delay times of hemoglobin S gelation prevent most cells from sickling in vivo
5. Kinetics and mechanism of deoxyhemoglobin S gelation: A new approach to understanding sickle cell disease
6. Microvascular sites and characteristics of sickle cell adhesion to vascular endothelium in shear flow conditions: Pathophysiological implications
7. Demonstration of endothelial adhesion of sickle cells in vivo: A distinct role for deformable sickle cell discocytes
8. Unusually large von Willebrand factor multimers increase adhesion of sickle erythrocytes to human endothelial cells under controlled flow
9. Unusually large von Willebrand factor multimers preferentially promote young sickle and nonsickle erythrocyte adhesion to endothelial cells
10. + sickle reticulocytes to endothelial cells
11. Thrombospondin from activated platelets promotes sickle erythrocyte adherence to human microvascular endothelium under physiologic flow: A potential role for platelet activation in sickle cell vaso-occlusion
12. 1-integrin expression on sickle reticulocytes: Vascular cell adhesion molecule-1-dependent binding to endothelium
13. Sickle reticulocytes adhere to VCAM-1
14. Double-stranded RNA induces sickle erythrocyte adherence to endothelium: A potential role for viral infection in vaso-occlusive pain episodes in sickle cell anemia
15. 1 integrin receptors on sickle reticulocytes and fibronectin
16. Adhesion of sickle red blood cells and damage to interleukin-1β stimulated endothelial cells under flow in vitro
17. P-selectin mediates the adhesion of sickle erythrocytes to the endothelium
18. Band 3 peptides block the adherence of sickle cells to endothelial cells in vitro
19. Glycoprotein IV-independent adhesion of sickle red blood cells to immobilized thrombospondin under flow conditions
20. Increased adhesion of erythrocytes to components of the extracellular matrix: Isolation and characterization of a red blood cell lipid that binds thrombospondin and laminin
21. Adherence of phosphatidylserine-exposing erythrocytes to endothelial matrix thrombospondin
22. Activation of sickle red blood cell adhesion via integrin-associated protein/CD47-induced signal transduction
23. Integrin-associated protein is an adhesion receptor on sickle red blood cells for immobilized thrombospondin
24. Sickle erythrocyteendothelial interactions in microcirculation: The role of von Willebrand factor and implications for vaso-occlusion
25. Disturbance of plasma and platelet thrombospondin levels in sickle cell disease
26. Red blood cells from patients with sickle cell disease exhibit an increased adherence to cultured endothelium pretreated with tumor necrosis factor (TNF)
27. Erythrocyte/endothelial interactions in the pathogenesis of sickle cell disease: A "real logical" assessment
28. Pluronic F-68 reduces the endothelial adherence and improves rheology of liganded sickle erythrocytes
29. Effects of density and dehydration of sickle cells on their adhesion to cultured endothelial cells
30. Blood viscosity, mass transport, and thrombogenesis
31. Periodic microcirculatory flow in patients with sickle-cell disease
32. Intravital microscopy of capillary hemodynamics in sickle cell disease
33. In vivo blood flow abnormalities in the transgenic knockout sickle cell mouse
34. The contribution of sialic acid to the surface charge of the erythrocyte
35. Differences in erythrocyte membrane proteins and glycoproteins in sickle cell disease
36. A Schiff base with mildly oxidized carbohydrate ligands stabilized L-selectin and P-selectin rolling adhesions in shear flow
37. Activation of vascular endothelial cell adhesion molecule expression by sickle blood cells
38. Leukocyte cell surface enzymology: CD45 (LCA, T200) is a protein tyrosine kinase phosphatase
39. A counter-rotating "rheoscope chamber" for the study of microrheology of blood cell aggregation microscopic observation and microphotometry
40. Improved in vitro rheological system for studying the effect of fluid shear stress on cultured cells
41. A criterion for purely tangential laminar flow in the cone and plate rheometer and the parallel-plate rheometer
42. A review of mathematical models for the prediction of blood cell adhesion
43. Platelet deposition on subendothelium exposed to flowing blood: Mathematical analysis of physical parameters
44. Molecular basis of sickle cell-endothelial cell interactions
45. Adherence of sickle erythrocytes to vascular endothelial cells: Requirements for both cell membrane changes and plasma factors
46. Abnormalities in membrane phospholipid organization in sickled erythrocytes
47. Sickled erythrocytes accelerate clotting in vitro: An effect of abnormal membrane lipid asymmetry
48. Alteration of red cell membrane organization in sickle cell disease
49. Cell-bound autologous immunoglobulin in erythrocyte subpopulations from patients with sickle cell disease
50. Excessive binding of natural anti-α-galactosyl immunoglobin G to sickle erythrocytes may contribute to extravascular destruction
51. Sickle erythrocyte adherence to endothelium. Morphologic correlates and the requirement for divalent cations and collagen-binding plasma proteins
52. Adhesive interactions of sickle erythrocytes with endothelium
53. The flow of model particles and blood cells and its relation to thrombogenesis
54. Microscopic considerations: The motions of individual particles
55. Physics of cell adhesion
56. The biochemistry of cell adhesion
57. Hydrodynamics of interaction of particles (including cells) with surfaces
58. Adherence properties of sickle erythrocytes in dynamic flow systems
59. Shear rate dependency of red cell sequestration in skin capillaries in sickle cell disease and its variation with vaso-occlusive crisis
60. Rheological aspects of sickle cell disease