Nicolas Alice, Besser Achim, Safran Samuel A
Laboratoire de Physique de la Matière Condensée, Université de Nice-CNRS, France.
Biophys J. 2008 Jul;95(2):527-39. doi: 10.1529/biophysj.107.127399. Epub 2008 Apr 11.
Cell focal adhesions are micrometer-sized aggregates of proteins that anchor the cell to the extracellular matrix. Within the cell, these adhesions are connected to the contractile, actin cytoskeleton; this allows the adhesions to transmit forces to the surrounding matrix and makes the adhesion assembly sensitive to the rigidity of their environment. In this article, we predict the dynamics of focal adhesions as a function of the rigidity of the substrate. We generalize previous theories and include the fact that the dynamics of proteins that adsorb to adhesions are also driven by their coupling to cell contractility and the deformation of the matrix. We predict that adhesions reach a finite size that is proportional to the elastic compliance of the substrate, on a timescale that also scales with the compliance: focal adhesions quickly reach a relatively small, steady-state size on soft materials. However, their apparent sliding is not sensitive to the rigidity of the substrate. We also suggest some experimental probes of these ideas and discuss the nature of information that can be extracted from cell force microscopy on deformable substrates.
细胞粘着斑是将细胞锚定到细胞外基质的微米级蛋白质聚集体。在细胞内部,这些粘着斑与收缩性的肌动蛋白细胞骨架相连;这使得粘着斑能够将力传递到周围的基质,并使粘着斑组装对其环境的刚性敏感。在本文中,我们预测粘着斑的动力学作为底物刚性的函数。我们推广了先前的理论,并纳入了这样一个事实,即吸附到粘着斑上的蛋白质的动力学也受到它们与细胞收缩性和基质变形的耦合驱动。我们预测粘着斑会达到一个与底物的弹性顺应性成正比的有限大小,在一个也与顺应性成比例的时间尺度上:粘着斑在软材料上会迅速达到相对较小的稳态大小。然而,它们明显的滑动对底物的刚性不敏感。我们还提出了一些对这些观点的实验探测方法,并讨论了可以从可变形底物上的细胞力显微镜中提取的信息的性质。