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A multiscale continuum model is constructed for a mechanosensitive (MS) channel gated by tension in a lipid bilayer membrane under stresses due to fluid flows. We illustrate that for typical physiological conditions vesicle hydrodynamics driven by a fluid flow may render the membrane tension sufficiently large to gate a MS channel open. In particular, we focus on the dynamic opening/ closing of a MS channel in a vesicle membrane under a planar shear flow and a pressure-driven flow across a constriction channel. Our modeling and numerical simulation results quantify the critical flow strength or flow channel geometry for intracellular transport through a MS channel. In particular, we determine the percentage of MS channels that are open or closed as a function of the relevant measure of flow strength. The modeling and simulation results imply that for fluid flows that are physiologically relevant and realizable in microfluidic configurations stress-induced intracellular transport across the lipid membrane can be achieved by the gating of reconstituted MS channels, which can be useful for designing drug delivery in medical therapy and understanding complicated mechanotransduction. [ABSTRACT FROM AUTHOR]

Using a rod theory formulation, we derive equations of state for a thin elastic membrane subjected to several different boundary conditions--clamped, simply supported, and periodic. The former is applicable to membranes supported on a softer substrate and subjected to uniaxial compression. We show that a wider family of quasistatic equilibrium shapes exist beyond the previously obtained analytical solutions. In the latter case of periodic membranes, we were able to derive exact solutions in terms of elliptic functions. These equilibria are verified by considering a fluid-structure interaction problem of a periodic, length-preserving bilipid membrane modeled by the Helfrich energy immersed in a viscous fluid. Starting from an arbitrary shape, the membrane dynamics to equilibrium are simulated using a boundary integral method. [ABSTRACT FROM AUTHOR]