Ward M D, Hammer D A
School of Chemical Engineering, Cornell University, Ithaca, NY 14853.
Cell Biophys. 1992 Apr-Jun;20(2-3):177-222. doi: 10.1007/BF02823657.
Many cell types modulate growth, differentiation, and motility through changes in cell substrate adhesion, including regulation of focal contact formation. Clustering of cell surface adhesion receptors is an essential early step in the development of focal contacts, and thus may influence cell physiology. In this paper, we present a theoretical framework to examine how cell surface chemistry affects receptor clustering. Our one-dimensional tape-peeling model couples the equations of mechanical equilibrium for a cell membrane with kinetic receptor-ligand binding relations. We considered two distinct model scenarios: Adhesion mediated by multiple receptor-ligand interactions of different length and specific binding of a single receptor type occurs in the presence of van der Waals attraction and nonspecific repulsion. In each case, nonuniform (wave-like) membrane morphologies are observed in certain parameter ranges that support the clustering of adhesion receptors. The formation of these morphologies is described in terms of a balance of membrane stresses; when cell-surface potential as a function of separation distance is symmetric between two potential energy minima, nonuniform morphologies are obtained. Increases in the chemical binding energy between receptor and ligand (e.g., increases in ligand density) or decreases in the membrane rigidity result in smaller wavelengths for nonuniform interfaces. Additionally, we show wave-like geometries appear only when the mechanical compliance of receptor-ligand bonds is within an intermediate range, and examine how the mobility of "repellers"--glycocalyx molecules that exert a nonspecific repulsive force--influences membrane morphology. We find fully mobile repellers always redistribute to prevent nonuniform morphologies.
许多细胞类型通过改变细胞与底物的粘附来调节生长、分化和运动,包括调节粘着斑的形成。细胞表面粘附受体的聚集是粘着斑形成过程中必不可少的早期步骤,因此可能影响细胞生理功能。在本文中,我们提出了一个理论框架来研究细胞表面化学如何影响受体聚集。我们的一维胶带剥离模型将细胞膜的力学平衡方程与受体 - 配体结合的动力学关系相结合。我们考虑了两种不同的模型情况:由不同长度的多种受体 - 配体相互作用介导的粘附以及在范德华引力和非特异性排斥存在的情况下单一受体类型的特异性结合。在每种情况下,在支持粘附受体聚集的特定参数范围内观察到非均匀(波状)的膜形态。这些形态的形成是根据膜应力的平衡来描述的;当作为分离距离函数的细胞表面电势在两个势能最小值之间对称时,就会获得非均匀形态。受体与配体之间化学结合能的增加(例如配体密度的增加)或膜刚性的降低会导致非均匀界面的波长变小。此外,我们表明只有当受体 - 配体键的机械顺应性处于中间范围内时才会出现波状几何形状,并研究“排斥剂”(即施加非特异性排斥力的糖萼分子)的流动性如何影响膜形态。我们发现完全可移动的排斥剂总是重新分布以防止形成非均匀形态。