Helenius Jonne, Heisenberg Carl-Philipp, Gaub Hermann E, Muller Daniel J
Biotechnology Center, University of Technology Dresden, Germany.
J Cell Sci. 2008 Jun 1;121(11):1785-91. doi: 10.1242/jcs.030999.
The controlled adhesion of cells to each other and to the extracellular matrix is crucial for tissue development and maintenance. Numerous assays have been developed to quantify cell adhesion. Among these, the use of atomic force microscopy (AFM) for single-cell force spectroscopy (SCFS) has recently been established. This assay permits the adhesion of living cells to be studied in near-physiological conditions. This implementation of AFM allows unrivaled spatial and temporal control of cells, as well as highly quantitative force actuation and force measurement that is sufficiently sensitive to characterize the interaction of single molecules. Therefore, not only overall cell adhesion but also the properties of single adhesion-receptor-ligand interactions can be studied. Here we describe current implementations and applications of SCFS, as well as potential pitfalls, and outline how developments will provide insight into the forces, energetics and kinetics of cell-adhesion processes.
细胞彼此之间以及与细胞外基质的可控黏附对于组织发育和维持至关重要。已经开发了许多测定方法来量化细胞黏附。其中,原子力显微镜(AFM)用于单细胞力谱(SCFS)的应用最近已被确立。该测定法允许在接近生理条件下研究活细胞的黏附。AFM的这种应用实现了对细胞无与伦比的空间和时间控制,以及高度定量的力驱动和力测量,其灵敏度足以表征单分子之间的相互作用。因此,不仅可以研究整体细胞黏附,还可以研究单个黏附受体-配体相互作用的特性。在这里,我们描述了SCFS的当前应用和潜在陷阱,并概述了这些进展将如何深入了解细胞黏附过程的力、能量学和动力学。