Abstract

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.

Highlights

  • Cell-mimetic systems play an important role in gaining insights into the physical basis of cell adhesion and are ideal to study how the mobility, density and topography of cell adhesion molecules (CAMs) affect the formation of bonds

  • Since the binding energy of membrane bound CAM–CAM pairs is strongly dependent on the thermo-mechanical properties of the composite cell envelope and the actin cortex, the osmotic pressure of unbound CAMs, and generic interfacial forces, these relationships have to be established in order to relate the measurements of single molecule unbinding forces to the binding energy of CAM–CAM pairs embedded in cell membranes

  • Giant vesicles containing small amounts of attractive CAMs mediated the formation of strong speci c inter-membrane links with co-receptors of target membranes

Read more

Summary

View Article Online

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. Since 1970 he has been focusing on the physics of biological membranes, cell adhesion and cell mechanics He has received a number of awards for his work and is today considered one of the pioneers of biophysics in Europe. S. was recruited to the Physics department of the University Erlangen-Nurnberg, as a Rising Star of the Excellence Cluster: Engineering of Advanced Materials There she established the PULS group and was tenured in 2012. Her research focuses on problems in so matter and biophysics

Introduction
Biomimetic models of cell adhesion
Bending elasticity model of soft shell adhesion
Modulation of adhesion strength by membrane bending excitations
Soft shell adhesion as a heterogeneous wetting process
Adhesion domain stabilisation by actin cortex
Control of cell adhesion by receptor inhibitors
Immunological synapses
Conclusions and perspectives
Future challenges
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.