体外流动剪切力作用下的白细胞-内皮细胞动态粘附

建立一个用于体外研究特定流动剪切力作用下白细胞和内皮细胞动态相互作用的方法。利用建立的平板流动小室系统可在体外产生特定的流动剪切力。将培养的人脐静脉内皮细胞装入平板流动小室后 ,以 0 .71dynes/cm2 的流动剪切力把含有吖啶橙染色的白细胞的灌流液导入流动小室 ,由此产生了白细胞和内皮细胞的动态粘附过程。整个粘附过程通过OlympusIX70倒置荧光显微系统观察 ,同时通过CCD摄象头录像。然后用图象采集卡将录像采集为数字图象并保存。利用针对实验设计的图象处理和分析方法 ,对采集的数字图象进行处理和测量 ,可以得到粘附白细胞的个数和滚动白细胞的速度。通过研究内毒素脂多糖 (LPS)对内皮细胞粘附功能的促进及地塞米松 (DXM )对该刺激的抑制作用来验证。对于用内毒素脂多糖 (LPS)处理的内皮细胞 ,固定粘附和慢速滚动的白细胞的个数比对照组分别显著增加了 2 3.7倍和 4 .1倍 ,同时白细胞在粘附作用过程中慢速滚动和快速滚动的速度比对照组明显降低了 2 5 .6 %和 2 6 .1%。而对于脂多糖和地塞米松 (DXM)处理过的内皮细胞 ,上述内毒素引起的影响被显著抑制了。该方法可以用于研究不同的化学和物理刺激对内皮细胞功能的影响机制 ,及用来评价各类抑制内皮细胞粘附功能的药物。

Dynamic Investigation of Leukocyte-Endothelial Cell Adhesion Interaction under Fluid Shear Stress in Vitro

To establish a method to investigate the dynamic adhesion between leukocytes and human umbilical vein endothelial cells (HUVECs) under definite shear stress. A parallel plate flow chamber system was developed to produce the definite shear stress in vitro. After the cultured HUVECs were loaded in the flow chamber, the circulation solution containing acridine orange (AO)-labeled leukocytes was perfused to flow through chamber at 0.71 dynes/cm2. In this case, leukocyte-endothelial cell adhesion process was induced. Lipopolysaccharide(LPS) was used as the chemical stimulus and dexamethasone(DXM) was used as the anti-inflammatory reagent. The adhesion process was recorded in videotape by Olympus IX70 fluorescence microscope and CCD-camera. Then the number of adhesion leukocyte, slow and fast rolling velocities of leukocytes on the surface of HUVECs were measured based on the captured images. The number of static adhering and slow rolling leukocytes on the HUVECs treated with LPS was significantly increased by 23.7-fold and 4.1-fold compared with that of the control group. Meanwhile, both the slow and fast rolling velocities of the leukocytes on HUVECs treated with LPS were significantly decreased by 25.6% and 26.1%. When HUVECs were treated with both LPS and DXM, the effect of LPS was inhibited obviously. This developed method can be used in studying ECs adhesion function affected by different chemical and physical stimulus and evaluating the various compounds interfering with cell adhesion.