Abstract

Physiologically relevant in vitro models of stretchable biological tissues, such as muscle, lung, cardiac and gastro-intestinal tissues, should mimic the mechanical cues which cells are exposed to in their dynamic microenvironment in vivo. In particular, in order to mimic the mechanical stimulation of tissues in a physiologically relevant manner, cell stretching is often desirable on surfaces with dynamically controllable curvature. Here, we present a device that can deform cell culture membranes without the current need for external pneumatic/fluidic or electrical motors, which typically make the systems bulky and difficult to operate. We describe a modular device that uses elastomeric membranes, which can intrinsically be deformed by electrical means, producing a dynamically tuneable curvature. This approach leads to compact, self-contained, lightweight and versatile bioreactors, not requiring any additional mechanical equipment. This was obtained via a special type of dielectric elastomer actuator. The structure, operation and performance of early prototypes are described, showing preliminary evidence on their ability to induce changes on the spatial arrangement of the cytoskeleton of fibroblasts dynamically stretched for 8 h.

Highlights

  • All biological tissues are subjected to internal mechanical forces that arise from interstitial flows and cellular motions

  • As an alternative to conventional hydraulic/fluidic systems that can achieve an analogous effect, we present a dielectric elastomer actuators (DEAs)-based modular device made of elastomeric membranes that are deformable electrically, without any fluidic system

  • We described a novel bioreactor to cyclically stretch cells in vitro, via electrically deformable elastomeric membranes with a dynamically tuneable curvature

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Summary

Introduction

All biological tissues are subjected to internal mechanical forces that arise from interstitial flows and cellular motions These forces can redistribute effector molecules that are secreted by cells, resulting in the coupling of chemical and mechanical signaling. Most of the commercially available devices for cell stretching in vitro are actuated by pneumatic systems, such as those from Flexcell R (Flexcell International, 2019), or mechanical motors, such as those from Strex R (Strex Inc, 2019). They require external driving units (vacuum pumps or motors), which make the systems bulky, complex to operate, acoustically noisy and generally capable of low throughput (Brown, 2000)

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