Erythrocyte deformability responses to intermittent and continuous subhemolytic shear stress

Biorheology

Volumn 51, Issue 2-3, 2014, Pages 171-185

  Simmonds, Michael J ^a   Atac, Nazli ^b   Baskurt, Oguz K ^b   Meiselman, Herbert J ^c   Yalcin, Ozlem ^b  

^a GRIFFITH UNIVERSITY   (Australia)

^b KOÇ UNIVERSITY   (Turkey)

^c UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

deformability; exposure time; Mechanical damage; red blood cell; shear stress

Indexed keywords

HEMOGLOBIN;

ADULT; BLOOD SAMPLING; CARDIOVASCULAR SYSTEM; CELL DAMAGE; CELL ELONGATION; CONFERENCE PAPER; CONTROLLED STUDY; CYTOMETRY; EKTACYTOMETRY; ERYTHROCYTE DEFORMABILITY; ERYTHROCYTE STRUCTURE; HEMOGLOBIN BLOOD LEVEL; HEMOLYSIS; HUMAN; HUMAN CELL; HUMAN EXPERIMENT; LONG TERM EXPOSURE; MECHANICAL STRESS; MICROVASCULATURE; NORMAL HUMAN; SHEAR STRESS; STEADY STATE; SUBHEMOLYTIC THRESHOLD; ERYTHROCYTE; FEMALE; MALE; PHYSIOLOGY;

ERYTHROCYTE DEFORMABILITY; ERYTHROCYTES; FEMALE; HEMOLYSIS; HUMANS; MALE; STRESS, MECHANICAL;

EID: 84925346099     PISSN: 0006355X     EISSN: 18785034     Source Type: Journal    
DOI: 10.3233/BIR-140665     Document Type: Conference Paper

References (36)

1. O.K. Baskurt, M.R. Hardeman, M. Uyuklu, P. Ulker, M. Cengiz, N. Nemeth et al., Parameterization of red blood cell elongation index-shear stress curves obtained by ektacytometry, Scand. J. Clin. Lab. Invest. 69 (2009), 777-788.
2. O.K. Baskurt and H.J. Meiselman, Blood rheology and hemodynamics, Semin. Thromb. Hemost. 29 (2003), 435-450.
3. O.K. Baskurt and H.J. Meiselman, Red blood cell mechanical stability test, Clin. Hemorheol. Microcirc. 55 (2013), 55-62.
4. O.K. Baskurt and H.J. Meiselman, Data reduction methods for ektacytometry in clinical hemorheology, Clin. Hemorheol. Microcirc. 54 (2013), 99-107.
5. O.K. Baskurt, M. Uyuklu and H.J. Meiselman, Protection of erythrocytes from sub-hemolytic mechanical damage by nitric oxide mediated inhibition of potassium leakage, Biorheology 41 (2004), 79-89.
6. O.K. Baskurt, O. Yalcin and H.J. Meiselman, Hemorheology and vascular control mechanisms, Clin. Hemorheol. Micro-circ. 30(3) (2004), 169-178.
7. J.D. Baure, Laboratory investigation of hemoglobin, in: Gradwohl's Clinical Laboratory Methods and Diagnosis, A.C. Sonnenwirth and L. Jarett, eds, Mosby, St. Louis, MO, 1980, pp. 809-902.
8. M. Bor-Kucukatay, R.B. Wenby, H.J. Meiselman and O.K. Baskurt, Effects of nitric oxide on red blood cell deformability, Am. J. Physiol. Heart Circ. Physiol. 284 (2003), H1577-H1584.
9. D.E. Brinsfield, M.A. Hopf, R.B. Geering and P.M. Galletti, Hematological changes in long-term perfusion, J. Appl. Physiol. 17 (1962), 531-534.
10. S. Chien, Red cell deformability and its relevance to blood flow, Annu. Rev. Physiol. 49 (1987), 177-192.
11. M. Grau, S. Pauly, J. Ali, K. Walpurgis, M. Thevis, W. Bloch et al., RBC-NOS-dependent S-nitrosylation of cytoskeletal proteins improves RBC deformability, PLoS One 8 (2013), e56759.
12. Y.J. Gu, R. Graaff, E. de Hoog, N.J. Veeger, G. Panday, P.W. Boonstra et al., Influence of hemodilution of plasma proteins on erythrocyte aggregability: an in vivo study in patients undergoing cardiopulmonary bypass, Clin. Hemorheol. Microcirc. 33 (2005), 95-107.
13. M.R. Hardeman, P.T. Goedhart and N.H. Schut, Laser-assisted optical rotational cell analyser (L.O.R.C.A.); II. Red blood cell deformability: Elongation index versus cell transit time, Clin. Hemorheol. Microcirc. 14 (1994), 619-630.
14. M.V. Kameneva, A. Undar, J.F. Antaki, M.J. Watach, J.H. Calhoon and H.S. Borovetz, Decrease in red blood cell deforma-bility caused by hypothermia, hemodilution, and mechanical stress: factors related to cardiopulmonary bypass, ASAIO J. 45 (1999), 307-310.
15. A.G. Koutsiaris, S.V. Tachmitzi and N. Batis, Wall shear stress quantification in the human conjunctival pre-capillary arterioles in vivo, Microvasc. Res. 85 (2013), 34-39.
16. S.S. Lee, K.H. Ahn, S.J. Lee, K. Sun, P.T. Goedhart and M.R. Hardeman, Shear induced damage of red blood cells monitored by the decrease of their deformability, Korea-Australia Rheology Journal 16 (2004), 141-146.
17. L.B. Leverett, J.D. Hellums, C.P. Alfrey and E.C. Lynch, Red blood cell damage by shear stress, Biophys. J. 12 (1972), 257-273.
18. H.H. Lipowsky, L.E. Cram, W. Justice and M.J. Eppihimer, Effect of erythrocyte deformability on in vivo red cell transit time and hematocrit and their correlation with in vitro filterability, Microvasc. Res. 46 (1993), 43-64.
19. A.M. Malek, S.L. Alper and S. Izumo, Hemodynamic shear stress and its role in atherosclerosis, JAMA 282 (1999), 2035-2042.
20. P.J. Marascalco, S.P. Ritchie, T.A. Snyder and M.V. Kameneva, Development of standard tests to examine viscoelastic properties of blood of experimental animals for pediatric mechanical support device evaluation, ASAIO J. 52 (2006), 567-574.
21. E. Meram, B.D. Yilmaz, C. Bas, N. Atac, O. Yalcin, H.J. Meiselman et al., Shear stress-induced improvement of red blood cell deformability, Biorheology 50 (2013), 165-176.
22. T. Mizuno, T. Tsukiya, Y. Taenaka, E. Tatsumi, T. Nishinaka, H. Ohnishi et al., Ultrastructural alterations in red blood cell membranes exposed to shear stress, ASAIO J. 48 (2002), 668-670.
23. N. Mohandas, M.R. Clark, B.P. Health, M. Rossi, L.C. Wolfe, S.E. Lux et al., A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders, Blood 59 (1982), 768-774.
24. N. Mohandas, M.R. Clark, M.S. Jacobs and S.B. Shohet, Analysis of factors regulating erythrocyte deformability, J. Clin. Invest. 66 (1980), 563-573.
25. A.M. Morariu, Y.J. Gu, R.C. Huet, W.A. Siemons, G. Rakhorst and W.V. Oeveren, Red blood cell aggregation during cardiopulmonary bypass: a pathogenic cofactor in endothelial cell activation?, Eur. J. Cardiothorac. Surg. 26 (2004), 939-946.
26. Y. Morsi, M. Kogure and M. Umezu, Relative blood damage index of the jellyfish valve and the Bjork-Shiley tilting-disk valve, J. Artif. Organs 2 (1999), 163-169.
27. A.V. Muravyov and I.A. Tikhomirova, Role molecular signaling pathways in changes of red blood cell deformability, Clin. Hemorheol. Microcirc. 53 (2013), 45-59.
28. C.G. Nevaril, E.C. Lynch, C.P. Alfrey, Jr. and J.D. Hellums, Erythrocyte damage and destruction induced by shearing stress, J. Lab. Clin. Med. 71 (1968), 784-790.
29. T. Oonishi, K. Sakashita and N. Uyesaka, Regulation of red blood cell filterability by Ca2+ influx and cAMP-mediated signaling pathways, Am. J. Physiol. 273 (1997), C1828-C1834.
30. E.A. O'Rear, M.M. Udden, J.A. Farmer, L.V. McIntire and E.C. Lynch, Increased intracellular calcium and decreased deformability of erythrocytes from prosthetic heart-valve patients, Clinical Hemorheology 4 (1984), 461-471.
31. K. Parthasarathi and H.H. Lipowsky, Capillary recruitment in response to tissue hypoxia and its dependence on red blood cell deformability, Am. J. Physiol. 277 (1999), H2145-H2157.
32. J.G. Sandza, R.E. Clark, C.S. Weldon and S.P. Sutera, Subhemolytic trauma of erythrocytes: recognition and sequestration by the spleen as a function of shear, Trans. Am. Soc. Artif. Intern. Organs 20B (1974), 457-462.
33. R.S. Sprague, M.L. Ellsworth, A.H. Stephenson, M.E. Kleinhenz and A.J. Lonigro, Deformation-induced ATP release from red blood cells requires CFTR activity, Am. J. Physiol. 275 (1998), H1726-H1732.
34. S.P. Sutera and M.H. Mehrjardi, Deformation and fragmentation of human red blood cells in turbulent shear flow, Bio-phys. J. 15 (1975), 1-10.
35. P. Ulker, N. Yaras, O. Yalcin, C. Celik-Ozenci, P.C. Johnson, H.J. Meiselman et al., Shear stress activation of nitric oxide synthase and increased nitric oxide levels in human red blood cells, Nitric Oxide 24 (2011), 184-191.
36. J. Wan, W.D. Ristenpart and H.A. Stone, Dynamics of shear-induced ATP release from red blood cells, Proc. Natl. Acad. Sci. USA 105 (2008), 16432-16437.