Kaplanski G, Farnarier C, Tissot O, Pierres A, Benoliel A M, Alessi M C, Kaplanski S, Bongrand P
Laboratoire d'Immunologie, Hôpital de Sainte-Marguerite, Marseille, France.
Biophys J. 1993 Jun;64(6):1922-33. doi: 10.1016/S0006-3495(93)81563-7.
The adhesion of moving cells to receptor-bearing surfaces is a key step to many important biological processes. Attachment was subjected to extensive modeling. However, the numerical values of kinetic bonding parameters relevant to realistic models of cell adhesion remain poorly known. In this report, we describe the motion of human granulocytes to interleukin-1-activated endothelial cells in presence of a low hydrodynamic drag (a few piconewtons) estimated to be much weaker than a standard ligand-receptor bond. It was thus expected to visualize the formation and rupture of individual bonds. We observed multiple short-time cell arrests with a median duration of 2.43 s. Stop frequency, not duration, was significantly inhibited by anti-E-selectin antibodies. Binding efficiency exhibited an almost linear relationship with the inverse of cell velocity. The distribution of arrest duration was determined: results were consistent with the view that these arrests reflected the formation/dissociation of single ligand-receptor bonds with a spontaneous dissociation rate of 0.5 s-1. The rate of bond formation was on the order of 0.04 s-1 when cells were freely rolling (mean velocity: 19 microns/s) and it exhibited an approximately 10-fold increase after the formation of a first adhesion.
运动细胞与带有受体的表面的黏附是许多重要生物学过程的关键步骤。对细胞黏附进行了广泛的建模。然而,与细胞黏附的实际模型相关的动力学结合参数的数值仍然知之甚少。在本报告中,我们描述了在低流体动力阻力(几皮牛顿)存在的情况下,人类粒细胞向白细胞介素-1激活的内皮细胞的运动,该阻力估计比标准配体-受体键弱得多。因此,有望观察到单个键的形成和断裂。我们观察到多次短时间的细胞停滞,中位持续时间为2.43秒。抗E-选择素抗体显著抑制停滞频率,而非持续时间。结合效率与细胞速度的倒数呈现几乎线性的关系。确定了停滞持续时间的分布:结果与这些停滞反映单个配体-受体键的形成/解离且自发解离速率为0.5 s-1的观点一致。当细胞自由滚动时(平均速度:19微米/秒),键形成速率约为0.04 s-1,在形成第一个黏附后,键形成速率增加了约10倍。