Biomicrofluidics. 2011 Mar 30;5(1):13408. doi: 10.1063/1.3552998.
Axon path-finding plays an important role in normal and pathogenic brain development as well as in neurological regenerative medicine. In both scenarios, axonal growth is influenced by the microenvironment including the soluble molecules and contact-mediated signaling from guiding cells and cellular matrix. Microfluidic devices are a powerful tool for creating a microenvironment at the single cell level. In this paper, an asymmetrical-channel-based biochip, which can be later incorporated into microfluidic devices for neuronal network study, was developed to investigate geometric as well as supporting cell control of polarized axonal growth in forming a defined neuronal circuitry. A laser cell deposition system was used to place single cells, including neuron-glia pairs, into specific microwells of the device, enabling axonal growth without the influence of cytophilic∕phobic surface patterns. Phase microscopy showed that a novel "snag" channel structure influenced axonal growth in the intended direction 4:1 over the opposite direction. In heterotypic experiments, glial cell influence over the axonal growth path was observed with time-lapse microscopy. Thus, it is shown that single cell and heterotypic neuronal path-finding models can be developed in laser patterned biochips.
轴突寻路在正常和病理性脑发育以及神经再生医学中起着重要作用。在这两种情况下,轴突的生长都受到微环境的影响,包括来自指导细胞和细胞外基质的可溶性分子和接触介导的信号。微流控装置是在单细胞水平上创建微环境的有力工具。本文开发了一种基于非对称通道的生物芯片,可用于后续集成到微流控装置中,以研究几何形状和支持细胞对形成特定神经元回路的极化轴突生长的控制。激光细胞沉积系统用于将单个细胞(包括神经元-神经胶质对)放置在设备的特定微井中,从而实现无需细胞亲合力/疏水性表面图案影响的轴突生长。相差显微镜显示,新颖的“障碍”通道结构以 4:1 的比例影响了预期方向上的轴突生长,而不是相反方向。在异质型实验中,通过延时显微镜观察到神经胶质细胞对轴突生长路径的影响。因此,表明可以在激光图案化生物芯片中开发单细胞和异质型神经元寻路模型。