Abstract

Cells can feel and react to the mechanical properties of their environment such as stiffness or geometry by translating mechanical cues into biochemical ones, inducing biochemical and mechanical responses. This process, called mechanotransduction, drives critical functions such as cell differentiation, proliferation and migration. In order to assess to which extend cellular response depends on the temporal and spatial characteristics of the stimulation, it is essential to control temporally and spatially the mechanical cues. Methods have been proposed to apply global and continuous deformations, or local deformations though discrete substrates. Here we propose a novel method to apply mechanical stimuli in a local and dynamic way to cells plated on the continuous surface of deformable substrates. These substrates are made of a soft elastomer (PDMS) in which iron micro-pillars are embedded and actuated by two electromagnets. The amplitude of the surface deformation is controlled by the input current in the coils, and monitored by tracking fluorescent particles underneath the surface. Traction Force Microscopy (TFM) allows us to estimate the stress generated by the pillars, and the cellular mechanical response. Cells adhering to the magneto-active substrates can be stimulated both in traction and compression in the range of contractile cell stresses. Thanks to the compatibility with standard fluorescence techniques, we can furthermore observe the biochemical response of cells with fluorescence techniques such as quantitative Fluorescence Resonance Energy Transfer (FRET).

Highlights

  • 1602-Pos Board B511 Cell Growth Rate Dictates the Onset of Glass to Fluid-Like Transition and Long Time Super-Diffusion in an Evolving Cell Colony Abdul Malmi Kakkada, Xin Li, Himadri S

  • Recent studies of morphogenesis gastrulation in Drosophila and Xenopus hasve shown that the apical constriction of ventral furrow cells can be is driven by pulsed actomyosin contraction within medio-apical surface

  • Together with theoretical simulations based on Surface EvolverÒ, we can explain the morphological change by the change of apical surface tension

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Summary

Introduction

1602-Pos Board B511 Cell Growth Rate Dictates the Onset of Glass to Fluid-Like Transition and Long Time Super-Diffusion in an Evolving Cell Colony Abdul Malmi Kakkada, Xin Li, Himadri S. 1604-Pos Board B513 A Breakdown of Cellular Mechanisms Required for Cell and Focal Adhesion Area Sensitivity to Substrate Stiffness Magdalena Stolarska1, Aravind Rammohan2. Cell spread area and focal adhesion (FA) sizes are known to increase with substrate stiffness

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