IEEE Trans Biomed Eng. 2019 Jan;66(1):111-118. doi: 10.1109/TBME.2018.2835834. Epub 2018 May 14.
Cell patterning methods have been previously reported for cell culture. However, these methods use inclusions or devices that are not used in general cell culture and that might affect cell functionality. Here, we report a cell patterning method that can be conducted on a general cell culture dish without any inclusions by employing a resonance vibration of a disk-shaped ultrasonic transducer located under the dish. A resonance vibration with a single nodal circle patterned C2C12 myoblasts into a circular shape on the dish with 10-min exposure of the vibration with maximum peak-peak amplitude of 10 μm[Formula: see text]. Furthermore, the relationship between the amplitude distribution of the transducer and the cell density in the patterned sample could be expressed as a linear function, and there was a clear threshold of amplitude for cell adhesion. To evaluate the cell function of the patterned cells, we conducted proliferation and protein assays at 120-h culture after patterning. Our results showed that the cell proliferation rate did not decrease and the expression of cellular proteins was unchanged. Thus, we conclude, this method can successfully pattern cells in the clinically ubiquitous culture dish, while maintaining cell functionality.
细胞图案化方法以前曾被报道用于细胞培养。然而,这些方法使用了一般细胞培养中不使用的包含物或设备,这可能会影响细胞功能。在这里,我们报告了一种细胞图案化方法,该方法可以在没有任何包含物的情况下在普通细胞培养皿上进行,方法是利用位于培养皿下方的盘状超声换能器的共振振动。通过对振动进行 10 分钟的最大峰峰值幅度为 10μm 的振动暴露,可以将具有单个节点圆的共振振动将 C2C12 成肌细胞图案化成圆形。此外,换能器的振幅分布与图案化样本中的细胞密度之间的关系可以表示为线性函数,并且存在细胞粘附的明显振幅阈值。为了评估图案化细胞的细胞功能,我们在图案化后 120 小时的培养中进行了增殖和蛋白质分析。我们的结果表明,细胞增殖率没有下降,细胞蛋白的表达也没有改变。因此,我们得出结论,该方法可以成功地在临床上普遍存在的培养皿中对细胞进行图案化,同时保持细胞功能。