Physics of cell adhesion: some lessons from cell-mimetic systems

被引:99
作者
Sackmann, Erich [1 ,2 ]
Smith, Ana-Suncana [3 ,4 ]
机构
[1] Tech Univ Munich, Dept Phys, D-80290 Munich, Germany
[2] Univ Munich, Dept Phys, Munich, Germany
[3] Univ Erlangen Nurnberg, Inst Theoret Phys, Erlangen, Germany
[4] Rudjer Boskovic Inst, Zagreb, Croatia
关键词
RECEPTOR-LIGAND BONDS; SUPPORTED MEMBRANES; GIANT VESICLES; FLUID MEMBRANES; T-CELLS; FORCE; ACTIVATION; MODEL; GROWTH; ACTIN;
D O I
10.1039/c3sm51910d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cell adhesion is a paradigm of the ubiquitous interplay of cell signalling, modulation of material properties and biological functions of cells. It is controlled by competition of short range attractive forces, medium range repellant forces and the elastic stresses associated with local and global deformation of the composite cell envelopes. We review the basic physical rules governing the physics of cell adhesion learned by studying cell-mimetic systems and demonstrate the importance of these rules in the context of cellular systems. We review how adhesion induced micro-domains couple to the intracellular actin and microtubule networks allowing cells to generate strong forces with a minimum of attractive cell adhesion molecules (CAMs) and to manipulate other cells through filopodia over micrometer distances. The adhesion strength can be adapted to external force fluctuations within seconds by varying the density of attractive and repellant CAMs through exocytosis and endocytosis or protease-mediated dismantling of the CAM-cytoskeleton link. Adhesion domains form local end global biochemical reaction centres enabling the control of enzymes. Actin-microtubule crosstalk at adhesion foci facilitates the mechanical stabilization of polarized cell shapes. Axon growth in tissue is guided by attractive and repulsive clues controlled by antagonistic signalling pathways.
引用
收藏
页码:1644 / 1659
页数:16
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