Abstract

Mechanobiology-on-a-chip is a growing field focusing on how mechanical inputs modulate physico-chemical output in microphysiological systems. It is well known that biomechanical cues trigger a variety of molecular events and adjustment of mechanical forces is therefore essential for mimicking in vivo physiologies in organ-on-a-chip technology. Biomechanical inputs in organ-on-a-chip systems can range from variations in extracellular matrix type and stiffness and applied shear stresses to active stretch/strain or compression forces using integrated flexible membranes. The main advantages of these organ-on-a-chip systems are therefore (a) the control over spatiotemporal organization of in vivo-like tissue architectures, (b) the ability to precisely control the amount, duration and intensity of the biomechanical stimuli, and (c) the capability of monitoring in real time the effects of applied mechanical forces on cell, tissue and organ functions. Consequently, over the last decade a variety of microfluidic devices have been introduced to recreate physiological microenvironments that also account for the influence of physical forces on biological functions. In this review we present recent advances in mechanobiological lab-on-a-chip systems and report on lessons learned from these current mechanobiological models. Additionally, future developments needed to engineer next-generation physiological and pathological organ-on-a-chip models are discussed.

Highlights

  • Conventional mammalian cell culture systems are predominantly based on two-dimensional (2D) monolayer cultures to study cellular mechanisms in pharmaceutical research, toxicology and biomedicine

  • Biomechanical Cues in Organ-on-a-Chip Systems monolayers and native tissue structures leads in many cases to altered phenotype, cell morphology and behavior, rendering results from 2D cell-based assays questionable (Baker and Chen, 2012)

  • The implementation of 3D cell culture systems by itself allows for indirect mechanical stimulation by controlling the rigidity and stiffness of the extracellular matrix, which has shown to modulate cellular responses (Engler et al, 2006; Kumar, 2014)

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Summary

INTRODUCTION

Conventional mammalian cell culture systems are predominantly based on two-dimensional (2D) monolayer cultures to study cellular mechanisms in pharmaceutical research, toxicology and biomedicine. To date a variety of mechanobiological forces, shown, have been employed in 2D and 3D in vitro cultures including (a) matrix stiffness that mimic the respective Young’s moduli of native tissue, (b) fluid flow in vascular systems and interstitial tissue, (c) stretch/strain mechanisms in the lung, heart and gastrointestinal tract as well as (d) compression in the musculoskeletal system (Lovett et al, 2009; Riehl et al, 2012; Shachar et al, 2012; Ahearne, 2014) These mechanobiological systems demonstrated improved cell-to-cell and cell-to-matrix interactions resulting in significant progress in recapitulating physiological microenvironments in vitro.

Shear Stress
Gut Heart Muscle Vasculature
Compression and Other Novel Methods
MICROFLUIDIC MECHANOBIOLOGY IN THE THIRD DIMENSION
Interstitial Flow
CONCLUDING REMARKS AND FURTHER PERSPECTIVES
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