Institute of Quantum Optics, Leibniz University Hannover, 30167 Hannover, Germany.
Institute for Regenerative Medicine, Sechenov University, 119991 Moscow, Russia.
ACS Appl Mater Interfaces. 2021 Feb 24;13(7):7839-7853. doi: 10.1021/acsami.0c16616. Epub 2021 Feb 9.
Neural progenitor cells generated from human induced pluripotent stem cells (hiPSCs) are the forefront of ″brain-on-chip″ investigations. Viable and functional hiPSC-derived neuronal networks are shaping powerful models for evaluating the normal and abnormal formation of cortical circuits, understanding the underlying disease mechanisms, and investigating the response to drugs. They therefore represent a desirable instrument for both the scientific community and the pharmacological industry. However, culture conditions required for the full functional maturation of individual neurons and networks are still unidentified. It has been recognized that three-dimensional (3D) culture conditions can better emulate neuronal tissue development compared to 2D cultures and thus provide a more desirable approach. In this paper, we present the design and implementation of a 3D scaffold platform that supports and promotes intricate neuronal network development. 3D scaffolds were produced through direct laser writing by two-photon polymerization (2PP), a high-resolution 3D laser microstructuring technology, using the biocompatible and nondegradable photoreactive resin Dental LT Clear (DClear). Neurons developed and interconnected on a 3D environment shaped by vertically stacked scaffold layers. The developed networks could support different cell types. Starting at the day 50 of 3D culture, neuronal progenitor cells could develop into cortical projection neurons (CNPs) of all six layers, different types of inhibitory neurons, and glia. Additionally and in contrast to 2D conditions, 3D scaffolds supported the long-term culturing of neuronal networks over the course of 120 days. Network health and functionality were probed through calcium imaging, which revealed a strong spontaneous neuronal activity that combined individual and collective events. Taken together, our results highlight advanced microstructured 3D scaffolds as a reliable platform for the 3D modeling of neuronal functions.
由人诱导多能干细胞(hiPSCs)产生的神经祖细胞是“芯片上的大脑”研究的前沿。可行且功能正常的 hiPSC 衍生神经元网络正在为评估皮质回路的正常和异常形成、理解潜在疾病机制以及研究药物反应构建强大的模型。因此,它们代表了科学界和药理学工业的理想工具。然而,仍未确定个体神经元和网络充分功能成熟所需的培养条件。已经认识到,与 2D 培养相比,三维(3D)培养条件可以更好地模拟神经元组织的发育,因此提供了一种更理想的方法。在本文中,我们介绍了一种支持和促进复杂神经元网络发展的 3D 支架平台的设计和实现。通过双光子聚合(2PP)的直接激光写入生产 3D 支架,这是一种高分辨率 3D 激光微结构技术,使用生物相容性和不可降解的光反应树脂 Dental LT Clear(DClear)。在由垂直堆叠的支架层形成的 3D 环境中,神经元得以发育和相互连接。开发的网络可以支持不同的细胞类型。从 3D 培养的第 50 天开始,神经元祖细胞可以发育成为所有 6 层的皮质投射神经元(CNPs)、不同类型的抑制性神经元和神经胶质细胞。此外,与 2D 条件不同,3D 支架支持神经元网络在 120 天的过程中进行长期培养。通过钙成像探测网络健康和功能,揭示了一种强大的自发神经元活动,该活动结合了个体和集体事件。总的来说,我们的结果强调了先进的微结构 3D 支架作为 3D 神经元功能建模的可靠平台。