神经球
微流控
三维细胞培养
细胞培养
纳米技术
背景(考古学)
胚胎干细胞
神经科学
化学
生物
材料科学
成体干细胞
生物化学
基因
古生物学
遗传学
作者
Subhadra Nandi,Satyajit Ghosh,Satyajit Ghosh,Anindyasundar Adak,Rajsekhar Roy,Arijit Bera,Surajit Ghosh,Surajit Ghosh
标识
DOI:10.1021/acschemneuro.5c00016
摘要
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.
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