Nandi Subhadra, Ghosh Satyajit, Adak Anindyasundar, Roy Rajsekhar, Bera Arijit, Ghosh Surajit
Department of Bioscience & Bioengineering, Indian Institute of Technology Jodhpur, NH 65, Surpura Bypass Road, Karwar, Rajasthan 342037, India.
School of Chemistry, Pharmacy and Food Biosciences, University of Reading, Whiteknights, Reading RG6 6AH, U.K.
ACS Chem Neurosci. 2025 Aug 6;16(15):2785-2799. doi: 10.1021/acschemneuro.5c00016. Epub 2025 Jul 11.
Over the past few decades, rapid advancements among cell culture models have come up as valuable assets in neurobiological research to understand the complexities of the human brain, disease development and progression at cellular and molecular levels. However, conventional 2D cell culture methods often fail to provide deeper insights into the complex phenomenon of neural cytoarchitecture. This limitation has led to the development of neural organoids such as neurospheres, which offer a closer representation of several neuronal cells. Microfluidics-based neuronal culture platforms further enhance neurosphere generation by enabling precise spatiotemporal control of physical and chemical cues. Here we report the design and fabrication of a low-cost, novel microfluidic device using a cutting-edge and cost-effective xurography technique. We further performed primary neuron culture, forming neurospheres and single cells at varying seeding densities inside the microchannels. Furthermore, to validate the compatibility of the microfluidic device for neuronal disease model generation, we cultured SH-SY5Y cell lines and checked their differentiation inside the chamber. Additionally, we demonstrated the application of the fabricated device as a coculture model using astrocytes and neurons. Finally, in an Alzheimer's disease model context, we tested the device using a multitargeted compound, TDSB, with three important moieties to manage reactive oxygen species in the differentiated SH-SY5Y cells. The results revealed that TDSB can decrease metal-induced ROS generation and inhibit Aβ-Cu(II) induced cytotoxicity. Therefore, our multifaceted microfluidic device can open avenues for neuronal culture and coculture, neurodegenerative disease modeling, and screening of novel neurotherapeutic interventions.
在过去几十年中,细胞培养模型的快速发展已成为神经生物学研究中的宝贵资源,有助于在细胞和分子水平上理解人类大脑的复杂性、疾病的发展和进程。然而,传统的二维细胞培养方法往往无法深入洞察神经细胞结构的复杂现象。这一局限性促使了神经类器官(如神经球)的发展,神经球能更接近地模拟多种神经元细胞。基于微流控的神经元培养平台通过实现对物理和化学信号的精确时空控制,进一步提高了神经球的生成效率。在此,我们报告了一种使用前沿且经济高效的刻写技术设计和制造的低成本新型微流控装置。我们进一步在微通道内以不同的接种密度进行了原代神经元培养、形成神经球和单细胞。此外,为了验证该微流控装置用于生成神经元疾病模型的兼容性,我们培养了SH-SY5Y细胞系并检查了它们在腔室内的分化情况。此外,我们展示了所制造的装置作为星形胶质细胞和神经元共培养模型的应用。最后,在阿尔茨海默病模型背景下,我们使用一种具有三个重要部分的多靶点化合物TDSB对该装置进行了测试,以管理分化的SH-SY5Y细胞中的活性氧。结果表明,TDSB可以减少金属诱导的活性氧生成并抑制Aβ-Cu(II)诱导的细胞毒性。因此,我们的多功能微流控装置可为神经元培养和共培养、神经退行性疾病建模以及新型神经治疗干预的筛选开辟道路。