Laboratoire Matière et Systèmes Complexes, UMR CNRS 7057 Université Paris-Diderot, Paris, France.
Biophys J. 2011 Jul 20;101(2):336-44. doi: 10.1016/j.bpj.2011.06.009.
The coupling between cell-cell and cell-matrix adhesion systems is known to affect the stability of the adhesive status of cells, as well as tissue cohesion. In this work, we perform quantitative assays of integrin-cadherin cross talk in controlled and reproducible conditions. This is achieved by plating cells on microprinted fibronectin patterns of different sizes, and simulating the formation of an intercellular contact with a microbead coated with E-cadherin extracellular domains and brought to the cell membrane. Using an optical trap, we measure the average rigidity modulus of the E-cadherin bead-cell contact as a function of the contact incubation time and of the cell spreading area. For a given incubation time, this rigidity modulus decreases by three orders of magnitude as the cell-matrix contact area, A, increases from 100 to 700 μm(2). In a similar way, the dynamics of formation of the bead-cell contact gets slower as this area increases. This is clear evidence for a strong negative feedback from cell-fibronectin onto cell-cell adhesive contacts, for which we discuss some possible mechanisms.
细胞-细胞和细胞-基质黏附系统的偶联被认为会影响细胞黏附状态的稳定性以及组织内聚。在这项工作中,我们在可控且可重复的条件下对整合素-钙黏蛋白的串扰进行定量分析。具体做法是将细胞铺在大小不同的微印刷纤维连接蛋白图案上,并通过与带有 E-钙黏蛋白细胞外结构域的微珠模拟形成细胞间接触,使微珠与细胞膜接触。我们使用光阱测量 E-钙黏蛋白微珠-细胞接触的平均刚性模量作为接触孵育时间和细胞扩展面积的函数。对于给定的孵育时间,随着细胞-基质接触面积 A 从 100μm(2)增加到 700μm(2),刚性模量减小了三个数量级。以类似的方式,随着该区域的增加,微珠-细胞接触的形成动力学变得更慢。这有力地证明了细胞纤维连接蛋白对细胞间黏附接触的负反馈作用,我们对此讨论了一些可能的机制。