TY - JOUR
T1 - Biomechanics of cell rolling
T2 - Shear flow, cell-surface adhesion, and cell deformability
AU - Dong, Cheng
AU - Lei, Xiao X.
N1 - Funding Information:
The authors acknowledge Dr. Michael Lawrence at University of Virginia for providing P-selectin proteins. This study was supported in part by the Whitaker Foundation research grant and the NSF Career Award BES-9302079.
PY - 2000/1
Y1 - 2000/1
N2 - The mechanics of leukocyte (white blood cell; WBC) deformation and adhesion to endothelial cells (EC) has been investigated using a novel in vitro side-view flow assay. HL-60 cell rolling adhesion to surface-immobilized P-selectin was used to model the WBC-EC adhesion process. Changes in flow shear stress, cell deformability, or substrate ligand strength resulted in significant changes in the characteristic adhesion binding time, cell-surface contact and cell rolling velocity. A 2-D model indicated that cell-substrate contact area under a high wall shear stress (20dyn/cm2) could be nearly twice of that under a low stress (0.5dyn/cm2) due to shear flow-induced cell deformation. An increase in contact area resulted in more energy dissipation to both adhesion bonds and viscous cytoplasm, whereas the fluid energy that inputs to a cell decreased due to a flattened cell shape. The model also predicted a plateau of WBC rolling velocity as flow shear stresses further increased. Both experimental and computational studies have described how WBC deformation influences the WBC-EC adhesion process in shear flow. Copyright (C) 1999.
AB - The mechanics of leukocyte (white blood cell; WBC) deformation and adhesion to endothelial cells (EC) has been investigated using a novel in vitro side-view flow assay. HL-60 cell rolling adhesion to surface-immobilized P-selectin was used to model the WBC-EC adhesion process. Changes in flow shear stress, cell deformability, or substrate ligand strength resulted in significant changes in the characteristic adhesion binding time, cell-surface contact and cell rolling velocity. A 2-D model indicated that cell-substrate contact area under a high wall shear stress (20dyn/cm2) could be nearly twice of that under a low stress (0.5dyn/cm2) due to shear flow-induced cell deformation. An increase in contact area resulted in more energy dissipation to both adhesion bonds and viscous cytoplasm, whereas the fluid energy that inputs to a cell decreased due to a flattened cell shape. The model also predicted a plateau of WBC rolling velocity as flow shear stresses further increased. Both experimental and computational studies have described how WBC deformation influences the WBC-EC adhesion process in shear flow. Copyright (C) 1999.
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U2 - 10.1016/S0021-9290(99)00174-8
DO - 10.1016/S0021-9290(99)00174-8
M3 - Article
C2 - 10609516
AN - SCOPUS:0033991303
SN - 0021-9290
VL - 33
SP - 35
EP - 43
JO - Journal of Biomechanics
JF - Journal of Biomechanics
IS - 1
ER -