MIMETAS BV, Organ-On-a-Chip Company, 2333 CH, Leiden, The Netherlands.
Department of Translational Neuroscience, University Medical Center Utrecht Brain Center, Utrecht University, 3584 CG, Utrecht, The Netherlands.
Sci Rep. 2021 Jan 22;11(1):2080. doi: 10.1038/s41598-021-81335-z.
We report a method to generate a 3D motor neuron model with segregated and directed axonal outgrowth. iPSC-derived motor neurons are cultured in extracellular matrix gel in a microfluidic platform. Neurons extend their axons into an adjacent layer of gel, whereas dendrites and soma remain predominantly in the somal compartment, as verified by immunofluorescent staining. Axonal outgrowth could be precisely quantified and was shown to respond to the chemotherapeutic drug vincristine in a highly reproducible dose-dependent manner. The model was shown susceptible to excitotoxicity upon exposure with excess glutamate and showed formation of stress granules upon excess glutamate or sodium arsenite exposure, mimicking processes common in motor neuron diseases. Importantly, outgrowing axons could be attracted and repelled through a gradient of axonal guidance cues, such as semaphorins. The platform comprises 40 chips arranged underneath a microtiter plate providing both throughput and compatibility to standard laboratory equipment. The model will thus prove ideal for studying axonal biology and disease, drug discovery and regenerative medicine.
我们报告了一种生成具有分离和定向轴突生长的 3D 运动神经元模型的方法。将 iPSC 衍生的运动神经元在微流控平台中的细胞外基质凝胶中培养。神经元将其轴突延伸到相邻的凝胶层中,而树突和胞体主要保留在胞体隔室中,这通过免疫荧光染色得到证实。轴突生长可以精确地定量,并表现出对长春新碱等化疗药物的高度可重复的剂量依赖性反应。该模型在暴露于过量谷氨酸时易发生兴奋毒性,并在暴露于过量谷氨酸或砷酸钠时显示出应激颗粒的形成,模拟了运动神经元疾病中常见的过程。重要的是,通过轴突导向线索(如神经丝蛋白)的梯度可以吸引和排斥伸出的轴突。该平台由 40 个芯片组成,排列在微孔板下方,既提供了高通量,又与标准实验室设备兼容。因此,该模型将非常适合研究轴突生物学和疾病、药物发现和再生医学。