Barber K M, Pinero A, Truskey G A
Department of Biomedical Engineering, Duke University, Durham, North Carolina 27708-0281, USA.
Am J Physiol. 1998 Aug;275(2):H591-9. doi: 10.1152/ajpheart.1998.275.2.H591.
We used a sudden-expansion flow chamber to examine U-937 cell adhesion to unactivated and tumor necrosis factor (TNF)-alpha-activated human umbilical vein endothelial cells (HUVEC) in recirculating flow. For both unactivated and TNF-alpha-activated HUVEC, U-937 cells exhibited transient arrests within approximately 150 microm 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-alpha 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.
我们使用了一个突扩流动腔室,在循环流动中检测U - 937细胞与未激活及肿瘤坏死因子(TNF)-α激活的人脐静脉内皮细胞(HUVEC)的黏附情况。对于未激活及TNF -α激活的HUVEC,U - 937细胞在流动重新附着点约150微米范围内表现出短暂停滞。在重新附着点直接发生的停滞很少。未观察到U - 937细胞滚动。在循环区内的所有其他位置,U - 937细胞未表现出短暂停滞或滚动。TNF -α激活增加了U - 937细胞在重新附着点附近停滞的频率,但未改变停滞持续时间的中位数。数值模拟的细胞轨迹未能预测在重新附着点附近的附着情况。实验与理论之间的偏差可能源于U - 937细胞的非球形形状和可变形性。这些结果表明,U - 937细胞短暂停滞优先发生在循环流动中重新附着点附近。黏附的可能机制包括低剪切应力、弯曲的流线、垂直于内皮的流体速度分量以及更大接触面积的形成。