Guo Qiuquan, Liu Mei, Yang Jun
Biomedical Engineering Program, The University of Western Ontario, London, Ontario N6A 5B9, Canada.
Biosystems. 2011 Nov;106(2-3):130-5. doi: 10.1016/j.biosystems.2011.07.007. Epub 2011 Aug 5.
Intercellular interactions, which are mediated by a variety of complex intercellular molecules through the processes of formation and dissociation of molecular bonds, play a critical role in regulating cellular functions in biological systems. Various approaches are applied to evaluate intercellular or molecular bonding forces. To quantify the intermolecular interaction forces, flow chamber has become a meaningful technique as it can ultimately mimic the cellular microenvironment in vivo under physiological flow conditions. Hydrodynamic forces are usually used to predict the intercellular forces down to the single molecular level. However, results show that only using hydrodynamic force will overestimate up to 30% of the receptor-ligand strength when the non-specific forces such as Derjaguin-Landau-Verway-Overbeek (DLVO) forces become un-neglected. Due to the nature of high ion concentration in the physiological condition, electrostatic force is largely screened which will cause DLVO force unbalanced. In this study, we propose to take account of the DLVO force, including van der Waals (VDW) force and electrostatic force, to predict the intermolecular forces of a cell doublet and cell-substrate model in a circulating system. Results also show that the DLVO force has a nonlinear effect as the cell-cell or cell-substrate distance changes. In addition, we used the framework of high accuracy hydrodynamic theories proved in colloidal systems. It is concluded that DLVO force could not be ignored in quantitative studies of molecular interaction forces in circulating system. More accurate prediction of intercellular forces needs to take account of both hydrodynamic force and DLVO force.
细胞间相互作用通过分子键的形成和解离过程,由多种复杂的细胞间分子介导,在调节生物系统中的细胞功能方面发挥着关键作用。人们应用各种方法来评估细胞间或分子间的结合力。为了量化分子间相互作用的力,流动腔室已成为一项有意义的技术,因为它能够在生理流动条件下最终模拟体内的细胞微环境。流体动力通常被用于预测直至单分子水平的细胞间力。然而,结果表明,当诸如德亚金-朗道-维韦-奥弗贝克(DLVO)力等非特异性力变得不可忽略时,仅使用流体动力会高估受体-配体强度达30%。由于生理条件下高离子浓度的性质,静电力在很大程度上被屏蔽,这将导致DLVO力失衡。在本研究中,我们建议考虑DLVO力,包括范德华(VDW)力和静电力,以预测循环系统中细胞双联体和细胞-底物模型的分子间力。结果还表明,随着细胞-细胞或细胞-底物距离的变化,DLVO力具有非线性效应。此外,我们使用了在胶体系统中得到证明的高精度流体动力学理论框架。得出的结论是,在循环系统分子相互作用力的定量研究中,DLVO力不可忽略。对细胞间力更准确的预测需要同时考虑流体动力和DLVO力。