Yasuda Kenji
Department of Life Sciences, Graduate School of Arts and Sciences, University of Tokyo, 3-8-1 Komaba, Meguro, Tokyo 153-8902, Japan.
J Mol Recognit. 2004 May-Jun;17(3):186-93. doi: 10.1002/jmr.672.
We have developed an on-chip single-cell based microcultivation method for analyzing the variability of genetic information stored in single cells and their epigenetic correlations. The method uses four systems: an on-chip cell sorter for purifying the cells in a non-destructive manner; an on-chip single-cell cultivation chip for isolating single cells; an on-chip agarose microchamber system for constructive cell-cell network formation during cultivation; and an on-chip single-cell-based expression analysis system. Using these systems, we could measure the variability of prokaryotic cells and eukaryotic cells having the same DNA and found that, although prokaryotic cells have a large variability in their interdivision times, sister eukaryotic cells having the same DNA synchronized well. We also measured the dynamics of synchronization of beating cardiac myocytes and found that two isolated cells synchronize by one cell following the other after a short pause in beating. These results showed the potential of the on-chip microcultivation method's constructive approach to analyzing cell systems.
我们开发了一种基于芯片的单细胞微培养方法,用于分析存储在单细胞中的遗传信息的变异性及其表观遗传相关性。该方法使用四个系统:一个用于以非破坏性方式纯化细胞的芯片上细胞分选仪;一个用于分离单细胞的芯片上单细胞培养芯片;一个用于在培养过程中构建细胞-细胞网络的芯片上琼脂糖微腔系统;以及一个基于芯片的单细胞表达分析系统。使用这些系统,我们能够测量具有相同DNA的原核细胞和真核细胞的变异性,发现尽管原核细胞在分裂间隔时间上有很大的变异性,但具有相同DNA的姐妹真核细胞同步良好。我们还测量了跳动心肌细胞同步的动力学,发现两个分离的细胞在跳动短暂停顿后,一个细胞跟随另一个细胞同步。这些结果显示了芯片上微培养方法的建设性方法在分析细胞系统方面的潜力。