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配体的流动性调节细胞黏附和铺展。

Ligand Mobility-Mediated Cell Adhesion and Spreading.

机构信息

Department of Mechanical Engineering, The University of Hong Kong, Hong Kong 000000, China.

Department of Mechanics and Aerospace Engineering, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.

出版信息

ACS Appl Mater Interfaces. 2022 Mar 23;14(11):12976-12983. doi: 10.1021/acsami.1c22603. Epub 2022 Mar 13.

Abstract

Cells live in a highly dynamic environment where their physical connection and communication with the outside are achieved through receptor-ligands binding. Therefore, a precise knowledge of the interaction between receptors and ligands is critical for our understanding of how cells execute different biological duties. Interestingly, recent evidence has shown that the mobility of ligands at the cell-extracellular matrix (ECM) interface significantly affects the adhesion and spreading of cells, while the underlying mechanism remains unclear. Here, we present a modeling investigation to address this critical issue. Specifically, by adopting the Langevin dynamics, the random movement of ligands was captured by assigning a stochastic force along with a viscous drag on them. After that, the evolution of adhesion and subsequent spreading of cells were analyzed by considering the force-regulated binding/breakage of individual molecular bonds connecting polymerizing actin bundles inside the cell to the ECM. Interestingly, a biphasic relationship between adhesion and ligand diffusivity was predicted, resulting in maximized cell spreading at intermediate mobility of ligand molecules. In addition, this peak position was found to be dictated by the aggregation of ligands, effectively reducing their diffusivity, and how fast bond association/dissociation can occur. These predictions are in excellent agreement with our experimental observations where distinct ligand mobility was introduced by tuning the interactions between the self-assembly polymer coating and the surface.

摘要

细胞生活在一个高度动态的环境中,它们通过受体-配体结合与外界建立物理连接和通讯。因此,精确了解受体和配体之间的相互作用对于我们理解细胞如何执行不同的生物学功能至关重要。有趣的是,最近的证据表明,细胞-细胞外基质(ECM)界面上配体的流动性显著影响细胞的黏附和铺展,但其潜在机制尚不清楚。在这里,我们提出了一个建模研究来解决这个关键问题。具体来说,通过采用朗之万动力学,通过沿它们施加随机力和粘性阻力来捕获配体的随机运动。之后,通过考虑连接细胞内聚合肌动蛋白束和 ECM 的单个分子键的力调节结合/断裂,分析了细胞黏附和随后铺展的演变。有趣的是,在配体扩散率的中间范围内,预测到了黏附与配体扩散率之间的双相关系,从而导致细胞铺展最大化。此外,发现该峰位置由配体的聚集决定,有效降低了它们的扩散率,以及键的缔合/解离的速度。这些预测与我们的实验观察结果非常吻合,通过调整自组装聚合物涂层与表面之间的相互作用,可以引入不同的配体流动性。

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