Saterbak A, Kuo S C, Lauffenburger D A
Department of Chemical Engineering, University of Illinois, Urbana- Champaign 61801.
Biophys J. 1993 Jul;65(1):243-52. doi: 10.1016/S0006-3495(93)81077-4.
Biospecific cell adhesion is mediated by receptor-ligand bonds. Early theoretical work presented a deterministic analysis of receptor-mediated cell attachment and detachment for a homogeneous cell population. However, initial comparison of a deterministic framework to experimental detachment profiles of model "cells" (antibody-coated latex beads) did not show qualitative or quantitative agreement (Cozens-Roberts, C., D.A. Lauffenburger, and J.A. Quinn. 1990. Biophys. J. 58:857-872). Hence, we determine the contributions of population heterogeneity and probabilistic binding to the detachment behavior of this experimental system which was designed to minimize experimental and theoretical complications. This work also corrects an error in the numerical solution of the probabilistic model of receptor-mediated cell attachment and detachment developed previously (Cozens-Roberts, C., D.A. Lauffenburger, and J.A. Quinn. 1990. Biophys J. 58:841-856). Measurement of the population distribution of the number of receptors per bead has enabled us to explicitly consider the effect of receptor number heterogeneity within the cell-surface contact area. A deterministic framework that incorporates receptor number heterogeneity qualitatively and quantitatively accounts in large part for the model cell detachment data. Using measured and estimated parameter values for the model cell system, we estimate that about 90% of the observed kinetic detachment behavior originates from heterogeneity effects, while about 10% is due to probabilistic binding effects. In general, these relative contributions may differ for other systems.
生物特异性细胞黏附由受体 - 配体键介导。早期的理论工作对均匀细胞群体中受体介导的细胞附着和脱离进行了确定性分析。然而,将确定性框架与模型“细胞”(抗体包被的乳胶珠)的实验脱离曲线进行初步比较时,并未显示出定性或定量的一致性(科曾斯 - 罗伯茨,C.,D.A. 劳芬伯格,和 J.A. 奎因。1990.《生物物理杂志》58:857 - 872)。因此,我们确定了群体异质性和概率性结合对该实验系统脱离行为的贡献,该系统旨在尽量减少实验和理论上的复杂性。这项工作还纠正了先前开发的受体介导的细胞附着和脱离概率模型数值解中的一个错误(科曾斯 - 罗伯茨,C.,D.A. 劳芬伯格,和 J.A. 奎因。1990.《生物物理杂志》58:841 - 856)。对每个珠子上受体数量的群体分布进行测量,使我们能够明确考虑细胞表面接触区域内受体数量异质性的影响。一个纳入受体数量异质性的确定性框架在很大程度上定性和定量地解释了模型细胞的脱离数据。利用模型细胞系统的测量和估计参数值,我们估计观察到的动力学脱离行为中约90%源于异质性效应,而约10%归因于概率性结合效应。一般来说,对于其他系统,这些相对贡献可能会有所不同。