
- •Contents
- •Contributors
- •Preface
- •1 Introduction, with the biological basis for cell mechanics
- •Introduction
- •The role of cell mechanics in biological function
- •Maintenance of cell shape
- •Cell migration
- •Mechanosensing
- •Stress responses and the role of mechanical forces in disease
- •Active cell contraction
- •Structural anatomy of a cell
- •The extracellular matrix and its attachment to cells
- •Transmission of force to the cytoskeleton and the role of the lipid bilayer
- •Intracellular structures
- •Overview
- •References
- •2 Experimental measurements of intracellular mechanics
- •Introduction
- •Forces to which cells are exposed in a biological context
- •Methods to measure intracellular rheology by macrorheology, diffusion, and sedimentation
- •Whole cell aggregates
- •Sedimentation of particles
- •Diffusion
- •Mechanical indentation of the cell surface
- •Glass microneedles
- •Cell poker
- •Atomic force microscopy
- •Mechanical tension applied to the cell membrane
- •Shearing and compression between microplates
- •Optical traps
- •Magnetic methods
- •Twisting of magnetized particles on the cell surface and interior
- •Passive microrheology
- •Optically detected individual probes
- •One-particle method
- •Two-particle methods
- •Dynamic light scattering and diffusing wave spectroscopy
- •Fluorescence correlation spectroscopy
- •Optical stretcher
- •Acoustic microscopy
- •Outstanding issues and future directions
- •References
- •3 The cytoskeleton as a soft glassy material
- •Introduction
- •Magnetic Twisting Cytometry (MTC)
- •Measurements of cell mechanics
- •The structural damping equation
- •Reduction of variables
- •Universality
- •Scaling the data
- •Collapse onto master curves
- •Theory of soft glassy rheology
- •What are soft glassy materials
- •Sollich’s theory of SGMs
- •Soft glassy rheology and structural damping
- •Open questions
- •Biological insights from SGR theory
- •Malleability of airway smooth muscle
- •Conclusion
- •References
- •4 Continuum elastic or viscoelastic models for the cell
- •Introduction
- •Purpose of continuum models
- •Principles of continuum models
- •Boundary conditions
- •Mechanical and material characteristics
- •Example of studied cell types
- •Blood cells: leukocytes and erythrocytes
- •Limitations of continuum model
- •Conclusion
- •References
- •5 Multiphasic models of cell mechanics
- •Introduction
- •Biphasic poroviscoelastic models of cell mechanics
- •Analysis of cell mechanical tests
- •Micropipette aspiration
- •Cells
- •Biphasic properties of the pericellular matrix
- •Indentation studies of cell multiphasic properties
- •Analysis of cell–matrix interactions using multiphasic models
- •Summary
- •References
- •6 Models of cytoskeletal mechanics based on tensegrity
- •Introduction
- •The cellular tensegrity model
- •The cellular tensegrity model
- •Do living cells behave as predicted by the tensegrity model?
- •Circumstantial evidence
- •Prestress-induced stiffening
- •Action at a distance
- •Do microtubules carry compression?
- •Summary
- •Examples of mathematical models of the cytoskeleton based on tensegrity
- •The cortical membrane model
- •Tensed cable nets
- •Cable-and-strut model
- •Summary
- •Tensegrity and cellular dynamics
- •Conclusion
- •Acknowledgement
- •References
- •7 Cells, gels, and mechanics
- •Introduction
- •Problems with the aqueous-solution-based paradigm
- •Cells as gels
- •Cell dynamics
- •Gels and motion
- •Secretion
- •Muscle contraction
- •Conclusion
- •Acknowledgement
- •References
- •8 Polymer-based models of cytoskeletal networks
- •Introduction
- •The worm-like chain model
- •Force-extension of single chains
- •Dynamics of single chains
- •Network elasticity
- •Nonlinear response
- •Discussion
- •References
- •9 Cell dynamics and the actin cytoskeleton
- •Introduction: The role of actin in the cell
- •Interaction of the cell cytoskeleton with the outside environment
- •The role of cytoskeletal structure
- •Actin mechanics
- •Actin dynamics
- •The emergence of actin dynamics
- •The intrinsic dynamics of actin
- •Regulation of dynamics by actin-binding proteins
- •Capping protein: ‘decommissioning’ the old
- •Gelsolin: rapid remodeling in one or two steps
- •β4-thymosin: accounting (sometimes) for the other half
- •Dynamic actin in crawling cells
- •Actin in the leading edge
- •Monomer recycling: the other ‘actin dynamics’
- •The biophysics of actin-based pushing
- •Conclusion
- •Acknowledgements
- •References
- •10 Active cellular protrusion: continuum theories and models
- •Cellular protrusion: the standard cartoon
- •The RIF formalism
- •Mass conservation
- •Momentum conservation
- •Boundary conditions
- •Cytoskeletal theories of cellular protrusion
- •Network–membrane interactions
- •Network dynamics near the membrane
- •Special cases of network–membrane interaction: polymerization force, brownian and motor ratchets
- •Network–network interactions
- •Network dynamics with swelling
- •Other theories of protrusion
- •Numerical implementation of the RIF formalism
- •An example of cellular protrusion
- •Protrusion driven by membrane–cytoskeleton repulsion
- •Protrusion driven by cytoskeletal swelling
- •Discussion
- •Conclusions
- •References
- •11 Summary
- •References
- •Index
Active cellular protrusion: continuum theories and models |
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near the tip of a protrusion is increased, and that the permeability of the plasma membrane is sufficient to allow significant inflow from the extracellular environment. It is then possible for the volume of the protrusion to grow, and the filling with polymerized cytoskeleton is considered to take place after the fact for structural reasons. There are many problems with such a model – possibly explaining why it has lain fallow for a while, now. To mention just one problem, to the extent we are able to ascertain it, it appears that cellular volume does not change appreciably during the extension of protrusions, even big ones.
Shearing motor protrusion. At a most elementary level, myosin motors are shearing motors in the sense that they actively slide filaments parallel to one another. If one imagines a reasonably stiff assembly of cytoskeletal filaments perpendicular to the plasma membrane, it is conceivable that this structure could be driven out by a shearing motor mechanism as shown in Fig. 10-4 (Condeelis, 1993). Once of some popularity, this model seems more or less abandoned in the context of free protrusions, probably because there is evidence that molecular motors are not required – although we would caution that in our view, the case is far from being experimentally airtight.
Numerical implementation of the RIF formalism
A detailed discussion of the numerical strategies that can be used to solve the evolution equations is beyond the scope of this chapter. We will therefore limit ourselves to a brief outline of the methodology. Because it is well suited to free-boundary problems in the low-Reynolds-number limit, we use a Galerkin finite element scheme implemented in two spatial dimensions (for problems with cylindrical symmetry) on a mesh of quadrilateral cells. Grid and mass advection are implemented following cannonical methods that can be found in standard texts and reviews.
Briefly, the calculation is advanced over a time-step t determined by the Courant condition or other fast time scale of the dynamics. We evolve over t by means of sequential operations (this is operator splitting):
1.We advect the mesh boundary according to the network flow and then reposition mesh nodes for optimal resolution while preserving mesh topology, boundaries, and interfacial surfaces (Knupp and Steiberg, 1994).
2.We advect mass from the old mesh positions to the new mesh using a general Eulerian-Lagrangian scheme with upwind interpolation (Rash and Williamson, 1990).
3.We use constitutive laws to compute necessary quantities such as viscosities and surface tensions.
4.Finally, the momentum equations and the incompressibility condition together with the applicable boundary conditions are discretized using the Galerkin approach and the resulting system is solved for the pressure, network velocity, and solvent velocity on the advected mesh using an Uzawa style iteration (Temam, 1979).