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Department of Biomedical Engineering, Duke University, Durham, North Carolina 27708-0281
We used a sudden-expansion flow chamber to
examine U-937 cell adhesion to unactivated and tumor necrosis factor
(TNF)-
-activated human umbilical vein endothelial cells (HUVEC) in
recirculating flow. For both unactivated and TNF-
-activated HUVEC,
U-937 cells exhibited transient arrests within ~150 µm of flow
reattachment. Few arrests occurred directly at the reattachment site.
U-937 cell rolling was not observed. At all other locations within the recirculation zone, U-937 cells did not exhibit transient arrests or
rolling. TNF-
activation increased the frequency of U-937 cell
arrests near reattachment but did not change the median arrest duration. Numerically simulated cell trajectories failed to predict attachment near the reattachment point. Deviations between experiment and theory may result from the nonspherical shape and deformability of
U-937 cells. These results demonstrate that U-937 cell transient arrests occur preferentially in the vicinity of the reattachment point
in recirculating flow. Possible mechanisms for adhesion include low
shear stress, curved streamlines, fluid velocity components normal to
the endothelium, and formation of larger contact areas.
monocyte; atherosclerosis; hemodynamics
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