Hagiwara Soya, Tsuneishi Kazuhiro, Takada Naoya, Yasuda Kenji
Department of Pure and Applied Physics, Graduate School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku 169-8555, Tokyo, Japan.
Department of Physics, School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku 169-8555, Tokyo, Japan.
Gels. 2025 May 30;11(6):419. doi: 10.3390/gels11060419.
Constructing stable and flexible neuronal networks with multi-neurite wiring is essential for the in vitro modeling of brain function, connectivity, and neuroplasticity. However, most existing neuroengineering platforms rely on static microfabrication techniques, which limit the ability to dynamically control circuit architecture during cultivation. In this study, we developed a modifiable agarose gel-based platform that enables real-time microstructure fabrication using an infrared (IR) laser system under live-cell conditions. This approach allows for the stepwise construction of directional neurite paths, including sequential microchannel formation, cell chamber fabrication, and controlled neurite-neurite crossings. To support long-term neuronal health and network integrity in agarose microstructures, we incorporated direct glial co-culture into the system. A comparative analysis showed that co-culture significantly enhanced neuronal adhesion, neurite outgrowth, and survival over several weeks. The feeder layer configuration provided localized trophic support while maintaining a clear separation between glial and neuronal populations. Dynamic wiring experiments further confirmed the platform's precision and compatibility. Neurites extended through newly fabricated channels and crossed pre-existing neurites without morphological damage, even when laser fabrication occurred after initial outgrowth. Time-lapse imaging showed a temporary growth cone stalling at crossing points, followed by successful elongation in all tested samples. Furthermore, the direct laser irradiation of extending neurites during microstructure modification did not visibly impair neurite elongation, suggesting minimal morphological damage under the applied conditions. However, potential effects on molecular signaling and electrophysiological function remain to be evaluated in future studies. Together, these findings establish a powerful, flexible system for constructive neuroengineering. The platform supports long-term culture, real-time modification, and multidirectional wiring, offering new opportunities for studying neural development, synaptic integration, and regeneration in vitro.
构建具有多神经突布线的稳定且灵活的神经网络对于脑功能、连接性和神经可塑性的体外建模至关重要。然而,大多数现有的神经工程平台依赖于静态微制造技术,这限制了在培养过程中动态控制电路结构的能力。在本研究中,我们开发了一种基于可改性琼脂糖凝胶的平台,该平台能够在活细胞条件下使用红外(IR)激光系统进行实时微结构制造。这种方法允许逐步构建定向神经突路径,包括顺序微通道形成、细胞室制造以及受控的神经突 - 神经突交叉。为了支持琼脂糖微结构中神经元的长期健康和网络完整性,我们将直接胶质细胞共培养纳入该系统。一项比较分析表明,共培养在数周内显著增强了神经元的黏附、神经突生长和存活。饲养层配置提供了局部营养支持,同时保持了胶质细胞和神经元群体之间的清晰分离。动态布线实验进一步证实了该平台的精度和兼容性。神经突通过新制造的通道延伸并穿过预先存在的神经突而无形态损伤,即使在初始生长后进行激光制造也是如此。延时成像显示在交叉点处生长锥暂时停滞,随后在所有测试样本中成功伸长。此外,在微结构修饰过程中对延伸神经突的直接激光照射并未明显损害神经突伸长,这表明在所应用的条件下形态损伤最小。然而,对分子信号传导和电生理功能的潜在影响仍有待在未来研究中评估。总之,这些发现建立了一个强大、灵活的建设性神经工程系统。该平台支持长期培养、实时修饰和多向布线,为体外研究神经发育、突触整合和再生提供了新机会。