Ota Nobutoshi, Yalikun Yaxiaer, Tanaka Nobuyuki, Shen Yigang, Aishan Yusufu, Nagahama Yuki, Oikawa Minoru, Tanaka Yo
Center for Biosystems Dynamics Research, RIKEN.
Division of Materials Science, Nara Institute of Science and Technology.
Anal Sci. 2019 May 10;35(5):577-583. doi: 10.2116/analsci.18P568. Epub 2019 Jan 25.
Single cell analysis has gained attention as a means to investigate the heterogeneity of cells and amplify a cell with desired characteristics. However, obtaining a single cell from a large number of cells remains difficult because preparation of single-cell samples relies on conventional techniques such as pipetting that are labor intensive. In this study, we developed a system combining a 0.6-mm thin glass microfluidic device and machine vision approach to isolate single Euglena gracilis cells, as a model of microorganism with mobility, in a small/thin glass chamber. A single E. gracilis cell in a chamber was cultured for 4 days to monitor its multiplication. With this system, we successfully simplified preparation of single cells of interest and determined that it is possible to combine it with other analytical techniques to observe single cells continuously.
单细胞分析作为一种研究细胞异质性和扩增具有所需特性细胞的手段已受到关注。然而,从大量细胞中获取单个细胞仍然很困难,因为单细胞样本的制备依赖于诸如移液等传统技术,这些技术劳动强度大。在本研究中,我们开发了一种系统,该系统结合了一个0.6毫米厚的玻璃微流控装置和机器视觉方法,以在一个小而薄的玻璃腔室中分离作为具有运动性的微生物模型的单个纤细裸藻细胞。腔室内的单个纤细裸藻细胞培养4天以监测其增殖。通过该系统,我们成功简化了感兴趣的单个细胞的制备,并确定可以将其与其他分析技术相结合以连续观察单个细胞。