Geramifard Negar, Lawson Jennifer, Cogan Stuart F, Black Bryan James
Department of Bioengineering, Erik Jonsson School of Engineering and Computer Science, University of Texas at Dallas, Richardson, TX 75080, USA.
Biomedical Engineering Department, Francis College of Engineering, University of Massachusetts Lowell, Lowell, MA 01854, USA.
Micromachines (Basel). 2022 Oct 8;13(10):1692. doi: 10.3390/mi13101692.
Recent advances in cell and tissue engineering have enabled long-term three-dimensional (3D) in vitro cultures of human-derived neuronal tissues. Analogous two-dimensional (2D) tissue cultures have been used for decades in combination with substrate integrated microelectrode arrays (MEA) for pharmacological and toxicological assessments. While the phenotypic and cytoarchitectural arguments for 3D culture are clear, 3D MEA technologies are presently inadequate. This is mostly due to the technical challenge of creating vertical electrical conduction paths (or 'traces') using standardized biocompatible materials and fabrication techniques. Here, we have circumvented that challenge by designing and fabricating a novel helical 3D MEA comprised of polyimide, amorphous silicon carbide (a-SiC), gold/titanium, and sputtered iridium oxide films (SIROF). Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) testing confirmed fully-fabricated MEAs should be capable of recording extracellular action potentials (EAPs) with high signal-to-noise ratios (SNR). We then seeded induced pluripotent stems cell (iPSC) sensory neurons (SNs) in a 3D collagen-based hydrogel integrated with the helical MEAs and recorded EAPs for up to 28 days in vitro from across the MEA volume. Importantly, this highly adaptable design does not intrinsically limit cell/tissue type, channel count, height, or total volume.
细胞和组织工程学的最新进展使得人源神经组织能够进行长期的三维(3D)体外培养。类似的二维(2D)组织培养已被使用数十年,与基底集成微电极阵列(MEA)结合用于药理学和毒理学评估。虽然3D培养的表型和细胞结构优势很明显,但目前3D MEA技术还不完善。这主要是由于使用标准化生物相容性材料和制造技术创建垂直导电路径(或“迹线”)存在技术挑战。在此,我们通过设计和制造一种新型螺旋3D MEA规避了这一挑战,该MEA由聚酰亚胺、非晶碳化硅(a-SiC)、金/钛和溅射氧化铱薄膜(SIROF)组成。电化学阻抗谱(EIS)和循环伏安法(CV)测试证实,完全制造好的MEA应该能够以高信噪比(SNR)记录细胞外动作电位(EAP)。然后,我们将诱导多能干细胞(iPSC)感觉神经元(SN)接种到与螺旋MEA集成的基于3D胶原蛋白的水凝胶中,并在体外从MEA整个体积中记录EAP长达28天。重要的是,这种高度适应性的设计本质上并不限制细胞/组织类型、通道数量、高度或总体积。