Erdman Nick, Schmidt Lucas, Qin Wan, Yang Xiaoqi, Lin Yongliang, DeSilva Mauris N, Gao Bruce Z
Biofabrication. 2014 Sep;6(3):035025. doi: 10.1088/1758-5082/6/3/035025.
The ability to place individual cells into an engineered microenvironment in a cell-culture model is critical for the study of in vivo relevant cell-cell and cell-extracellular matrix interactions. Microfluidics provides a high-throughput modality to inject various cell types into a microenvironment. Laser guided systems provide the high spatial and temporal resolution necessary for single-cell micropatterning. Combining these two techniques, the authors designed, constructed, tested and evaluated (1) a novel removable microfluidics-based cell-delivery biochip and (2) a combined system that uses the novel biochip coupled with a laser guided cell-micropatterning system to place individual cells into both two-dimensional (2D) and three-dimensional (3D) arrays. Cell-suspensions of chick forebrain neurons and glial cells were loaded into their respective inlet reservoirs and traversed the microfluidic channels until reaching the outlet ports. Individual cells were trapped and guided from the outlet of a microfluidic channel to a target site on the cell-culture substrate. At the target site, 2D and 3D pattern arrays were constructed with micron-level accuracy. Single-cell manipulation was accomplished at a rate of 150 μm s(-1) in the radial plane and 50 μm s(-1) in the axial direction of the laser beam. Results demonstrated that a single-cell can typically be patterned in 20-30 s, and that highly accurate and reproducible cellular arrays and systems can be achieved through coupling the microfluidics-based cell-delivery biochip with the laser guided system.
在细胞培养模型中将单个细胞置于工程化微环境中的能力,对于研究体内相关的细胞-细胞和细胞-细胞外基质相互作用至关重要。微流控技术提供了一种高通量方式,可将各种细胞类型注入微环境。激光引导系统提供了单细胞微图案化所需的高空间和时间分辨率。结合这两种技术,作者设计、构建、测试并评估了:(1)一种新型的基于微流控的可移除细胞递送生物芯片;(2)一种组合系统,该系统使用新型生物芯片与激光引导细胞微图案化系统相结合,将单个细胞排列成二维(2D)和三维(3D)阵列。鸡前脑神经元和神经胶质细胞的细胞悬液被加载到各自的入口储液器中,并穿过微流控通道,直至到达出口端口。单个细胞被捕获,并从微流控通道的出口引导至细胞培养基质上的目标位点。在目标位点,以微米级精度构建了2D和3D图案阵列。在激光束的径向平面上,单细胞操作以150μm s(-1)的速度完成,在轴向方向上以50μm s(-1)的速度完成。结果表明,单个细胞通常可在20 - 30秒内进行图案化,并且通过将基于微流控的细胞递送生物芯片与激光引导系统相结合,可以实现高度精确且可重复的细胞阵列和系统。