Role of red blood cell flow behavior in hemodynamics and hemostasis

References

• Yedgar S, Koshkaryev A, Barshtein G. The red blood cell in vascular occlusion. Pathophysiol. Haemost. Thromb.32(5–6), 263–268 (2002).
   PubMedGoogle Scholar
• Ben-Ami R, Barshtein G, Mardi T et al. A synergistic effect of albumin and fibrinogen on immunoglobulin-induced red blood cell aggregation. Am. J. Physiol. Heart Circ. Physiol.285(6), H2663–H2669 (2003).
   PubMed Web of Science ®Google Scholar
• Shiga T, Maeda N, Kon K. Erythrocyte rheology. Crit. Rev. Oncol. Hematol.10(1), 9–48 (1990).
   PubMed Web of Science ®Google Scholar
• Chien S, Jan K. Ultrastructural basis of the mechanism of rouleaux formation. Microvasc. Res.5(2), 155–166 (1973).
   PubMed Web of Science ®Google Scholar
• Barshtein G, Tamir I, Yedgar S. Red blood cell rouleaux formation in dextran solution: dependence on polymer conformation. Eur. Biophys. J.27(2), 177–181 (1998).
   PubMed Web of Science ®Google Scholar
• Pribush A, Zilberman-Kravits D, Meyerstein N. The mechanism of the dextran-induced red blood cell aggregation. Eur. Biophys. J.36(2), 85–94 (2006).
   PubMed Web of Science ®Google Scholar
• Neu B, Meiselman HJ. Depletion-mediated red blood cell aggregation in polymer solutions. Biophys. J.83(5), 2482–2490 (2002).
   PubMed Web of Science ®Google Scholar
• Rampling MW, Meiselman HJ, Neu B, Baskurt OK. Influence of cell-specific factors on red blood cell aggregation. Biorheology41(2), 91–112 (2004).
   PubMed Web of Science ®Google Scholar
• Jan KM, Usami S, Chien S. The disaggregation effect of dextran 40 on red cell aggregation in macromolecular suspensions. Biorheology19(4), 543–554 (1982).
   PubMed Web of Science ®Google Scholar
• Armstrong JK, Meiselman HJ, Fisher TC. Covalent binding of poly(ethylene glycol) (PEG) to the surface of red blood cells inhibits aggregation and reduces low shear blood viscosity. Am. J. Hematol.56(1), 26–28 (1997).
   PubMed Web of Science ®Google Scholar
• Mohandas N, Chasis JA. Red blood cell deformability, membrane material properties and shape: regulation by transmembrane, skeletal and cytosolic proteins and lipids. Semin. Hematol.30(3), 171–192 (1993).
   PubMed Web of Science ®Google Scholar
• Hebbel RP, Moldow CF, Steinberg MH. Modulation of erythrocyte–endothelial interactions and the vasocclusive severity of sickling disorders. Blood58(5), 947–952 (1981).
   PubMed Web of Science ®Google Scholar
• Brittain HA, Eckman JR, Swerlick RA, Howard RJ, Wick TM. 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. Blood81(8), 2137–2143 (1993).
   PubMed Web of Science ®Google Scholar
• Maeda N, Kon K, Imaizumi K, Sekiya M, Shiga T. Alteration of rheological properties of human erythrocytes by crosslinking of membrane proteins. Biochim. Biophys. Acta735(1), 104–112 (1983).
   PubMedGoogle Scholar
• Nakajima T, Kon K, Maeda N, Tsunekawa K, Shiga T. Deformation response of red blood cells in oscillatory shear flow. Am. J. Physiol.259(4 Pt 2), H1071–H1078 (1990).
   PubMed Web of Science ®Google Scholar
• Ho M, Schollaardt T, Niu X et al. Characterization of Plasmodium falciparum-infected erythrocyte and P-selectin interaction under flow conditions. Blood91(12), 4803–4809 (1998).
   PubMed Web of Science ®Google Scholar
• Wen Z, Yao W, Xie L et al. Influence of neuraminidase on the characteristics of microrheology of red blood cells. Clin. Hemorheol. Microcirc.23(1), 51–57 (2000).
   PubMed Web of Science ®Google Scholar
• Martinez M, Vaya A, Gil L et al. The cholesterol/phospholipid ratio of the erythrocyte membrane in children with familial hypercholesterolemia. Its relationship with plasma lipids and red blood cell aggregability. Clin. Hemorheol. Microcirc.18(4), 259–263 (1998).
   PubMed Web of Science ®Google Scholar
• Sarr NG, Sall ND, Toure M, Diatta A, Seck I. [Phospholipid composition and content of the erythrocyte membrane in carriers of sickle cell trait]. Dakar Med.43(1), 5–8 (1998).
   PubMedGoogle Scholar
• Setty BN, Kulkarni S, Rao AK, Stuart MJ. Fetal hemoglobin in sickle cell disease: relationship to erythrocyte phosphatidylserine exposure and coagulation activation. Blood96(3), 1119–1124 (2000).
   PubMed Web of Science ®Google Scholar
• Manodori AB, Barabino GA, Lubin BH, Kuypers FA. Adherence of phosphatidylserine-exposing erythrocytes to endothelial matrix thrombospondin. Blood95(4), 1293–1300 (2000).
   PubMed Web of Science ®Google Scholar
• Junker M, Creutz CE. Ca(2+)-dependent binding of endonexin (annexin IV) to membranes: analysis of the effects of membrane lipid composition and development of a predictive model for the binding interaction. Biochemistry33(30), 8930–8940 (1994).
   PubMed Web of Science ®Google Scholar
• Telen MJ. Red blood cell surface adhesion molecules: their possible roles in normal human physiology and disease. Semin. Hematol.37(2), 130–142 (2000).
   PubMed Web of Science ®Google Scholar
• Eda K, Eda S, Sherman IW. Identification of peptides targeting the surface of Plasmodium falciparum-infected erythrocytes using a phage display peptide library. Am. J. Trop. Med. Hyg.71(2), 190–195 (2004).
   PubMed Web of Science ®Google Scholar
• Setty BN, Kulkarni S, Dampier CD, Stuart MJ. Fetal hemoglobin in sickle cell anemia: relationship to erythrocyte adhesion markers and adhesion. Blood97(9), 2568–2573 (2001).
   PubMed Web of Science ®Google Scholar
• Joneckis CC, Ackley RL, Orringer EP, Wayner EA, Parise LV. Integrin α 4 β 1 and glycoprotein IV (CD36) are expressed on circulating reticulocytes in sickle cell anemia. Blood82(12), 3548–3555 (1993).
   PubMed Web of Science ®Google Scholar
• van Schravendijk MR, Handunnetti SM, Barnwell JW, Howard RJ. Normal human erythrocytes express CD36, an adhesion molecule of monocytes, platelets, and endothelial cells. Blood80(8), 2105–2114 (1992).
   PubMed Web of Science ®Google Scholar
• Aruffo A, Stamenkovic I, Melnick M, Underhill CB, Seed B. CD44 is the principal cell surface receptor for hyaluronate. Cell61(7), 1303–1313 (1990).
   PubMed Web of Science ®Google Scholar
• Jalkanen S, Jalkanen M. Lymphocyte CD44 binds the COOH-terminal heparin-binding domain of fibronectin. J. Cell. Biol.116(3), 817–825 (1992).
   PubMed Web of Science ®Google Scholar
• Nunomura W, Takakuwa Y, Tokimitsu R et al. Regulation of CD44-protein 4.1 interaction by Ca2+ and calmodulin. Implications for modulation of CD44-ankyrin interaction. J. Biol. Chem.272(48), 30322–30328 (1997).
   PubMed Web of Science ®Google Scholar
• Kaul DK, Nagel RL, Chen D, Tsai HM. Sickle erythrocyte-endothelial interactions in microcirculation: the role of von Willebrand factor and implications for vasoocclusion. Blood81(9), 2429–2438 (1993).
   PubMed Web of Science ®Google Scholar
• Rattan V, Shen Y, Sultana C, Kumar D, Kalra VK. Diabetic RBC-induced oxidant stress leads to transendothelial migration of monocyte-like HL-60 cells. Am. J. Physiol.273(2 Pt 1), E369–E375 (1997).
   PubMedGoogle Scholar
• Chen S, Eldor A, Barshtein G et al. Enhanced aggregability of red blood cells of β-thalassemia major patients. Am. J. Physiol.270(6 Pt 2), H1951–H1956 (1996).
   PubMedGoogle Scholar
• Hovav T, Goldfarb A, Artmann G, Yedgar S, Barshtein G. Enhanced adherence of β-thalassaemic erythrocytes to endothelial cells. Br. J. Haematol.106(1), 178–181 (1999).
   PubMed Web of Science ®Google Scholar
• Yedgar S, Hovav T, Barshtein G. Red blood cell intercellular interactions in oxidative stress states. Clin. Hemorheol. Microcirc.21(3–4), 189–193 (1999).
   PubMed Web of Science ®Google Scholar
• Baskurt OK, Temiz A, Meiselman HJ. Effect of superoxide anions on red blood cell rheologic properties. Free Radic. Biol. Med.24(1), 102–110 (1998).
   PubMed Web of Science ®Google Scholar
• Ami RB, Barshtein G, Zeltser D et al. Parameters of red blood cell aggregation as correlates of the inflammatory state. Am. J. Physiol. Heart Circ. Physiol.280(5), H1982–H1988 (2001).
   PubMed Web of Science ®Google Scholar
• Ben-Ami R, Sheinman G, Yedgar S et al. Thrombolytic therapy reduces red blood cell aggregation in plasma without affecting intrinsic aggregability. Thromb. Res.105(6), 487–492 (2002).
   PubMed Web of Science ®Google Scholar
• Morrow DA, Rifai N, Antman EM et al. C-reactive protein is a potent predictor of mortality independently of and in combination with troponin T in acute coronary syndromes: a TIMI 11A substudy. Thrombolysis In Myocardial Infarction. J. Am. Coll. Cardiol.31(7), 1460–1465 (1998).
   PubMed Web of Science ®Google Scholar
• Samocha-Bonet D, Ben-Ami R, Shapira I et al. Flow-resistant red blood cell aggregation in morbid obesity. Int. J. Obes. Relat. Metab. Disord.28(12), 1528–1534 (2004).
   PubMed Web of Science ®Google Scholar
• Fusman R, Zeltser D, Rotstein R et al. INFLAMET: an image analyzer to display erythrocyte adhesiveness/aggregation. Eur. J. Intern. Med.11(5), 271–276 (2000).
   PubMedGoogle Scholar
• Maeda N, Shiga T. Opposite effect of albumin on the erythrocyte aggregation induced by immunoglobulin G and fibrinogen. Biochim. Biophys. Acta855(1), 127–135 (1986).
   PubMedGoogle Scholar
• Weng X, Roederer GO, Beaulieu R, Cloutier G. Contribution of acute-phase proteins and cardiovascular risk factors to erythrocyte aggregation in normolipidemic and hyperlipidemic individuals. Thromb. Haemost.80(6), 903–908 (1998).
   PubMed Web of Science ®Google Scholar
• Reinhart WH, Nagy C. Albumin affects erythrocyte aggregation and sedimentation. Eur. J. Clin. Invest.25(7), 523–528 (1995).
   PubMed Web of Science ®Google Scholar
• Parthasarathi K, Lipowsky HH. Capillary recruitment in response to tissue hypoxia and its dependence on red blood cell deformability. Am. J. Physiol.277(6 Pt 2), H2145–H2157 (1999).
   PubMedGoogle Scholar
• McHedlishvili G. Disturbed blood flow structuring as critical factor of hemorheological disorders in microcirculation. Clin. Hemorheol. Microcirc.19(4), 315–325 (1998).
   PubMed Web of Science ®Google Scholar
• Pantely GA, Swenson LJ, Tamblyn CH et al. Increased vascular resistance due to a reduction in red cell deformability in the isolated hind limb of swine. Microvasc. Res.35(1), 86–100 (1988).
   PubMed Web of Science ®Google Scholar
• Dikmenoglu N, Ciftci B, Ileri E et al. Erythrocyte deformability, plasma viscosity and oxidative status in patients with severe obstructive sleep apnea syndrome. Sleep Med.7(3), 255–261 (2006).
   PubMed Web of Science ®Google Scholar
• Bishop JJ, Nance PR, Popel AS, Intaglietta M, Johnson PC. Relationship between erythrocyte aggregate size and flow rate in skeletal muscle venules. Am. J. Physiol. Heart Circ. Physiol.286(1), H113–H120 (2004).
   PubMed Web of Science ®Google Scholar
• Kim S, Kong RL, Popel AS, Intaglietta M, Johnson PC. A computer-based method for determination of the cell-free layer width in microcirculation. Microcirculation13(3), 199–207 (2006).
   PubMed Web of Science ®Google Scholar
• Koscielny J, Jung EM, Mrowietz C, Kiesewetter H, Latza R. Blood fluidity, fibrinogen, and cardiovascular risk factors of occlusive arterial disease: results of the Aachen study. Clin. Hemorheol. Microcirc.31(3), 185–195 (2004).
   PubMed Web of Science ®Google Scholar
• Hebbel RP. Blockade of adhesion of sickle cells to endothelium by monoclonal antibodies. N. Engl. J. Med.342(25), 1910–1912 (2000).
   PubMed Web of Science ®Google Scholar
• Hebbel RP. Perspectives series: cell adhesion in vascular biology. Adhesive interactions of sickle erythrocytes with endothelium. J. Clin. Invest.99(11), 2561–2564 (1997).
   PubMed Web of Science ®Google Scholar
• Dhermy D, Simeon J, Wautier MP, Boivin P, Wautier JL. Role of membrane sialic acid content in the adhesiveness of aged erythrocytes to human cultured endothelial cells. Biochim. Biophys. Acta904(2), 201–206 (1987).
   PubMedGoogle Scholar
• Merrill EW, Cheng CS, Pelletier GA. Yield stress of normal human blood as a function of endogenous fibrinogen. J. Appl. Physiol.26(1), 1–3 (1969).
   PubMed Web of Science ®Google Scholar
• Bishop JJ, Nance PR, Popel AS, Intaglietta M, Johnson PC. Effect of erythrocyte aggregation on velocity profiles in venules. Am. J. Physiol. Heart Circ. Physiol.280(1), H222–H236 (2001).
   PubMed Web of Science ®Google Scholar
• Bishop JJ, Nance PR, Popel AS, Intaglietta M, Johnson PC. Erythrocyte margination and sedimentation in skeletal muscle venules. Am. J. Physiol. Heart Circ. Physiol.281(2), H951–H958 (2001).
   PubMed Web of Science ®Google Scholar
• Maeda N, Suzuki Y, Tanaka J, Tateishi N. Erythrocyte flow and elasticity of microvessels evaluated by marginal cell-free layer and flow resistance. Am. J. Physiol.271(6 Pt 2), H2454–H2461 (1996).
   PubMed Web of Science ®Google Scholar
• Suzuki Y, Tateishi N, Soutani M, Maeda N. Deformation of erythrocytes in microvessels and glass capillaries: effects of erythrocyte deformability. Microcirculation3(1), 49–57 (1996).
   PubMedGoogle Scholar
• Warkentin TE, Barr RD, Ali MA, Mohandas N. Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis. Blood75(1), 266–270 (1990).
   PubMed Web of Science ®Google Scholar
• Andrews DA, Low PS. Role of red blood cells in thrombosis. Curr. Opin. Hematol.6(2), 76–82 (1999).
   PubMedGoogle Scholar
• Hellem AJ, Borchgrevink CF, Ames SB. The role of red cells in haemostasis: the relation between haematocrit, bleeding time and platelet adhesiveness. Br. J. Haematol.7, 42–50 (1961).
   PubMed Web of Science ®Google Scholar
• Quaknine-Orlando B, Samama CM, Riou B et al. Role of the hematocrit in a rabbit model of arterial thrombosis and bleeding. Anesthesiology90(5), 1454–1461 (1999).
   PubMed Web of Science ®Google Scholar
• Soinne L, Saimanen E, Malmberg-Ceder K et al. Association of the fibrinolytic system and hemorheology with symptoms in patients with carotid occlusive disease. Cerebrovasc. Dis.20(3), 172–179 (2005).
   PubMed Web of Science ®Google Scholar
• Escolar G, Garrido M, Mazzara R, Castillo R, Ordinas A. Experimental basis for the use of red cell transfusion in the management of anemic-thrombocytopenic patients. Transfusion28(5), 406–411 (1988).
   PubMed Web of Science ®Google Scholar
• Gaudard A, Varlet-Marie E, Monnier JF et al. Exercise-induced central retinal vein thrombosis: possible involvement of hemorheological disturbances. A case report. Clin. Hemorheol. Microcirc.27(2), 115–122 (2002).
   PubMed Web of Science ®Google Scholar
• Berliner S, Rogowski O, Aharonov S et al. Erythrocyte adhesiveness/aggregation: a novel biomarker for the detection of low-grade internal inflammation in individuals with atherothrombotic risk factors and proven vascular disease. Am. Heart J.149(2), 260–267 (2005).
   PubMed Web of Science ®Google Scholar
• Assayag EB, Bornstein N, Shapira I et al. Inflammation-sensitive proteins and erythrocyte aggregation in atherothrombosis. Int. J. Cardiol.98(2), 271–276 (2005).
   PubMed Web of Science ®Google Scholar
• Sloop GD. A unifying theory of atherogenesis. Med. Hypotheses47(4), 321–325 (1996).
   PubMed Web of Science ®Google Scholar
• Aarts PA, Heethaar RM, Sixma JJ. Red blood cell deformability influences platelets – vessel wall interaction in flowing blood. Blood64(6), 1228–1233 (1984).
   PubMed Web of Science ®Google Scholar
• Uskudar O, Erdem A, Demiroglu H, Dikmenoglu N. Decreased erythrocyte deformability in Behcet’s disease. Clin. Hemorheol. Microcirc.33(2), 89–94 (2005).
   PubMed Web of Science ®Google Scholar
• Yasui K, Ohta K, Kobayashi M, Aizawa T, Komiyama A. Successful treatment of Behcet disease with pentoxifylline. Ann. Intern. Med.124(10), 891–893 (1996).
   PubMed Web of Science ®Google Scholar
• Brown MD, Wick TM, Eckman JR. Activation of vascular endothelial cell adhesion molecule expression by sickle blood cells. Pediatr. Pathol. Mol. Med.20(1), 47–72 (2001).
   PubMed Web of Science ®Google Scholar
• Stuart MJ, Setty BN. Acute chest syndrome of sickle cell disease: new light on an old problem. Curr. Opin. Hematol.8(2), 111–122 (2001).
   PubMed Web of Science ®Google Scholar
• Saldanha C, Sargento L, Monteiro J et al. Impairment of the erythrocyte membrane fluidity in survivors of acute myocardial infarction. A prospective study. Clin. Hemorheol. Microcirc.20(2), 111–116 (1999).
   PubMed Web of Science ®Google Scholar
• Mares M, Bertolo C, Terribile V, Girolami A. Hemorheological study in patients with coronary artery disease. Cardiology78(2), 111–116 (1991).
   PubMed Web of Science ®Google Scholar
• Kempe DS, Akel A, Lang PA et al. Suicidal erythrocyte death in sepsis. J. Mol. Med.85(3), 269–277 (2007).
   Web of Science ®Google Scholar
• Baskurt OK, Gelmont D, Meiselman HJ. Red blood cell deformability in sepsis. Am. J. Respir. Crit. Care Med.157(2), 421–427 (1998).
   PubMed Web of Science ®Google Scholar
• Negrean V, Suciu I, Sampelean D, Cozma A. Rheological changes in diabetic microangiopathy. Rom. J. Intern. Med.42(2), 407–413 (2004).
   PubMedGoogle Scholar
• Perez SM, Riquelme B, Acosta I, Valverde J, Milani A. Erythrocytes dynamic viscoelasticity in β-thalassaemia minor. Clin. Hemorheol. Microcirc.35(1–2), 311–316 (2006).
   PubMed Web of Science ®Google Scholar
• Nowak E, Wyrwicz G, Dabrowski Z, Smolenski O, Spodaryk K. Effects of phenylhydrazine or recombinant human erythropoietin on deformability and activity of dehydrogenase glucose-6-phosphate and acetylcholinesterase in Wistar rats blood enriched in reticulocytes. Folia Biol. (Krakow)51(3–4), 195–199 (2003).
   PubMed Web of Science ®Google Scholar
• Szapary L, Horvath B, Marton Z et al. Hemorheological disturbances in patients with chronic cerebrovascular diseases. Clin. Hemorheol. Microcirc.31(1), 1–9 (2004).
   PubMed Web of Science ®Google Scholar
• Ciuffetti G, Pasqualini L, Pirro M et al. Blood rheology in men with essential hypertension and capillary rarefaction. J. Hum. Hypertens.16(8), 533–537 (2002).
   PubMed Web of Science ®Google Scholar
• Thomas DJ. Rheology and strokes. Curr. Opin. Neurol. Neurosurg.5(1), 44–48 (1992).
   PubMedGoogle Scholar
• Stuart J, Johnson CS. Rheology of the sickle cell disorders. Baillieres Clin. Haematol.1(3), 747–775 (1987).
   PubMedGoogle Scholar
• Kaul DK, Liu XD, Zhang X et al. Inhibition of sickle red cell adhesion and vaso-occlusion in the microcirculation by antioxidants. Am. J. Physiol. Heart Circ. Physiol.291, H167–H175 (2006).
   PubMed Web of Science ®Google Scholar
• Barshtein G, Ponizovsky AM, Nechamkin Y et al. Aggregability of red blood cells of schizophrenia patients with negative syndrome is selectively enhanced. Schizophr. Bull.30(4), 913–922 (2004).
   PubMed Web of Science ®Google Scholar
• Wen Z, Xie J, Guan Z et al. A study of hemorheological behaviour for patients with Alzheimer’s disease at the early stages. Clin. Hemorheol. Microcirc.22(4), 261–266 (2000).
   PubMed Web of Science ®Google Scholar
• Hovav T, Yedgar S, Manny N, Barshtein G. Alteration of red cell aggregability and shape during blood storage. Transfusion39(3), 277–281 (1999).
   PubMed Web of Science ®Google Scholar
• Anniss AM, Sparrow RL. Storage duration and white blood cell content of red blood cell (RBC) products increases adhesion of stored RBCs to endothelium under flow conditions. Transfusion46(9), 1561–1567 (2006).
   PubMed Web of Science ®Google Scholar
• Berezina TL, Zaets SB, Morgan C et al. Influence of storage on red blood cell rheological properties. J. Surg. Res.102(1), 6–12 (2002).
   PubMed Web of Science ®Google Scholar
• Ben-Hur E, Barshtein G, Chen S, Yedgar S. Photodynamic treatment of red blood cell concentrates for virus inactivation enhances red blood cell aggregation: protection with antioxidants. Photochem. Photobiol.66(4), 509–512 (1997).
   PubMed Web of Science ®Google Scholar
• Hardeman MR, Besselink GA, Ebbing I et al. Laser-assisted optical rotational cell analyzer measurements reveal early changes in human RBC deformability induced by photodynamic treatment. Transfusion43(11), 1533–1537 (2003).
   PubMed Web of Science ®Google Scholar
• Adar T, Ben-Ami R, Elstein D et al. Aggregation of red blood cells in patients with Gaucher disease. Br. J. Haematol.134(4), 432–437 (2006).
   PubMed Web of Science ®Google Scholar