Abstract

Three-dimensional (3D) in vitro models have become increasingly popular as systems to study cell-cell and cell-ECM interactions dependent on the spatial, mechanical, and chemical cues within the environment of the tissue, which is limited in traditional two-dimensional (2D) models. Although electrophysiological recordings of neuronal action potentials through 2D microelectrode arrays (MEAs) are a common and trusted method of evaluating neuronal function, network communication, and response to chemicals and biologicals, there are currently limited options for measuring electrophysiological activity from many locations simultaneously throughout a 3D network of neurons in vitro. Here, we have developed a thin-film, 3D flexible microelectrode array (3DMEA) that non-invasively interrogates a 3D culture of neurons and can accommodate 256 channels of recording or stimulation. Importantly, the 3DMEA is straightforward to fabricate and integrates with standard commercially available electrophysiology hardware. Polyimide probe arrays were microfabricated on glass substrates and mechanically actuated to collectively lift the arrays into a vertical position, relying solely on plastic deformation of their base hinge regions to maintain vertical alignment. Human induced pluripotent stem cell (hiPSC)-derived neurons and astrocytes were entrapped in a collagen-based hydrogel and seeded onto the 3DMEA, enabling growth of suspended cells in the matrix and the formation and maturation of a neural network around the 3DMEA probes. The 3DMEA supported the growth of functional neurons in 3D with action potential spike and burst activity recorded over 45 days in vitro. This platform is an important step in facilitating noninvasive electrophysiological characterization of 3D networks of electroactive cells in vitro.

Highlights

  • Multi-electrode arrays (MEAs) provide a non-invasive method to monitor the electrophysiological activity of neurons in vitro over time

  • It was important that the device be biocompatible, relatively easy to fabricate, able to be integrated with existing commercial electrophysiology hardware, and straightforward to use for those preparing 3D cultures

  • It was desirable to have the 3D flexible microelectrode array (3DMEA) positioned in 3D space prior to cell–matrix addition, such that the cellular network could form naturally rather than inserting MEA probes into established neuronal cultures and thereby damaging the intricate neuronal network

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Summary

Introduction

Multi-electrode arrays (MEAs) provide a non-invasive method to monitor the electrophysiological activity of neurons in vitro over time. In an interconnected network of neurons, this can be observed as organized bursts of action potentials and/or synchronized activity that is detected across multiple electrodes on the array. The temporal and spatial organization and synchronization of action potentials can provide crucial insight into the health of and communication throughout a population of neurons.[3,4,5] For neurons cultured on a 2D surface, MEAs consisting of several thinfilm metal electrodes patterned on the cell growth surface are utilized.[18,19,20,21,22,23,24] As such, MEAs can record from many localized sites in parallel over long periods of time, providing a means to correlate activity across large populations of neurons and evaluate the system as an interconnected network. MEAs complement approaches that provide true intracellular recordings, such as patch clamping, that provide a greater level of detail regarding neuronal electrophysiological signalling

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