Recent studies indicate that the cell membrane, interacting with its attached cytoskeleton, is an important regulator of cell function, exerting and responding to forces. We investigate this relationship by looking for connections between cell membrane elastic properties, especially surface tension and bending modulus, and cell function. Those properties are measured by pulling tethers from the cell membrane with optical tweezers. Their values are determined for all major cell types of the central nervous system, as well as for macrophage. Astrocytes and glioblastoma cells, which are considerably more dynamic than neurons, have substantially larger surface tensions. Resting microglia, which continually scan their environment through motility and protrusions, have the highest elastic constants, with values similar to those for resting macrophage. For both microglia and macrophage, we find a sharp softening of bending modulus between their resting and activated forms, which is very advantageous for their acquisition of phagocytic functions upon activation. We also determine the elastic constants of pure cell membrane, with no attached cytoskeleton. For all cell types, the presence of F-actin within tethers, contrary to conventional wisdom, is confirmed. Our findings suggest the existence of a close connection between membrane elastic constants and cell function.

We propose to use optical tweezers to probe the Casimir interaction between microspheres inside a liquid medium for geometric aspect ratios far beyond the validity of the widely employed proximity force approximation. This setup has the potential for revealing unprecedented features associated to the non-trivial role of the spherical curvatures. For a proof of concept, we measure femtonewton double layer forces between polystyrene microspheres at distances above 400 nm by employing very soft optical tweezers, with stiffness of the order of fractions of a fN/nm. As a future application, we propose to tune the Casimir interaction between a metallic and a polystyrene microsphere in saline solution from attraction to repulsion by varying the salt concentration. With those materials, the screened Casimir interaction may have a larger magnitude than the unscreened one. This line of investigation has the potential for bringing together different fields including classical and quantum optics, statistical physics and colloid science, while paving the way for novel quantitative applications of optical tweezers in cell and molecular biology.

BackgroundThe viscoelastic properties of cells have been investigated by a variety of techniques. However, the experimental data reported in literature for viscoelastic moduli differ by up to three orders of magnitude. This has been attributed to differences in techniques and models for cell response as well as to the natural variability of cells.ResultsIn this work we develop and apply a new methodology based on optical tweezers to investigate the rheological behavior of fibroblasts, neurons and astrocytes in the frequency range from 1Hz to 35Hz, determining the storage and loss moduli of their membrane-cortex complex. To avoid distortions associated with cell probing techniques, we use a previously developed method that takes into account the influence of under bead cell thickness and bead immersion. These two parameters were carefully measured for the three cell types used. Employing the soft glass rheology model, we obtain the scaling exponent and the Young’s modulus for each cell type. The obtained viscoelastic moduli are in the order of Pa. Among the three cell types, astrocytes have the lowest elastic modulus, while neurons and fibroblasts exhibit a more solid-like behavior.ConclusionsAlthough some discrepancies with previous results remain and may be inevitable in view of natural variability, the methodology developed in this work allows us to explore the viscoelastic behavior of the membrane-cortex complex of different cell types as well as to compare their viscous and elastic moduli, obtained under identical and well-defined experimental conditions, relating them to the cell functions.Electronic supplementary materialThe online version of this article (doi:10.1186/s13628-016-0031-4) contains supplementary material, which is available to authorized users.

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Two force probing methods were used to quantify nanoscale forces in the interaction of the bacterial lectin LecA with the glycolipid Gb3, revealing how the interaction aids bacterial attachment and lowers the energy required for bacterial uptake.

Full-three-dimensional (3D) manipulation of individual glass beads with radii in the range of 2-8 μm is experimentally demonstrated by using a single Bessel light beam focused through a low-numerical-aperture lens (NA=0.40). Although we have a weight-assisted trap with the beam propagating upward, we obtain a stable equilibrium position well away from the walls of the sample cell, and we are able to move the particle across the entire cell in three dimensions. A theoretical analysis for the optical field and trapping forces along the lateral and axial directions is presented for the focused-Bessel trap. This trap offers advantages for 3D manipulation, such as an extended working distance, a large field of view, and reduced aberrations.

We unveil different regimes for the interaction between two orthogonally polarized soliton-like beams in a colloidal suspension of nanoparticles with positive polarizability. The interaction is always attractive. However, it noticeably changes as a function of the angle and the power distribution between the input beams. For small angles, both interacting solitons fuse into a single entity, whose propagation direction can be continuously steered. As the interaction angle increases, the resulting self-collimated beam can be practically switched between two positions when the power imbalance between the beams is changed. For interaction angles larger than ∼10°, the result is no longer a single emerging soliton when the input power is balanced between the two beams.

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