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Issue title: Workshop: Breaking Symmetry in Haemodynamics, London, UK, 23–24 April 2001
Article type: Research Article
Authors: Walker, P.G. | Alshorman, A.A. | Westwood, S. | David, T.
Affiliations: School of Mechanical Engineering, University of Leeds, Leeds, UK
Note: [] Address for correspondence: Dr. Peter G. Walker, School of Mechanical Engineering, University of Leeds, Leeds LS2 9JT, UK. Tel.: +44 113 343 2161; Fax: +44 113 242 4611; E‐mail: P.G.Walker@leeds.ac.uk.
Abstract: Leukocyte recruitment from blood to the endothelium plays an important role in atherosclerotic plaque formation. Cells show a primary and secondary adhesive process with primary bonds responsible for capture and rolling and secondary bonds for arrest. Our objective was to investigate the role played by this process on the adhesion of leukocytes in complex flow. Cells were modelled as rigid spheres with spring like adhesion molecules which formed bonds with endothelial receptors. Models of bond kinetics and Newton's laws of motion were solved numerically to determine cell motion. Fluid force was obtained from the local shear rate obtained from a CFD simulation of the flow over a backward facing step. In stagnation point flow the shear rate near the stagnation point has a large gradient such that adherent cells in this region roll to a high shear region preventing permanent adhesion. This is enhanced if a small time dependent perturbation is imposed upon the stagnation point. For lower shear rates the cell rolling velocity may be such that secondary bonds have time to form. These bonds resist the lower fluid forces and consequently there is a relatively large permanent adhesion region.
Keywords: Atherosclerosis, hemodynamics, mathematical modelling, rolling, CFD
Journal: Biorheology, vol. 39, no. 3-4, pp. 475-481, 2002
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