Sakaue-Sawano Asako, Kurokawa Hiroshi, Morimura Toshifumi, Hanyu Aki, Hama Hiroshi, Osawa Hatsuki, Kashiwagi Saori, Fukami Kiyoko, Miyata Takaki, Miyoshi Hiroyuki, Imamura Takeshi, Ogawa Masaharu, Masai Hisao, Miyawaki Atsushi
Laboratory for Cell Function and Dynamics, Advanced Technology Development Group, Brain Science Institute, RIKEN, 2-1 Hirosawa, Wako-city, Saitama 351-0198, Japan.
Cell. 2008 Feb 8;132(3):487-98. doi: 10.1016/j.cell.2007.12.033.
The cell-cycle transition from G1 to S phase has been difficult to visualize. We have harnessed antiphase oscillating proteins that mark cell-cycle transitions in order to develop genetically encoded fluorescent probes for this purpose. These probes effectively label individual G1 phase nuclei red and those in S/G2/M phases green. We were able to generate cultured cells and transgenic mice constitutively expressing the cell-cycle probes, in which every cell nucleus exhibits either red or green fluorescence. We performed time-lapse imaging to explore the spatiotemporal patterns of cell-cycle dynamics during the epithelial-mesenchymal transition of cultured cells, the migration and differentiation of neural progenitors in brain slices, and the development of tumors across blood vessels in live mice. These mice and cell lines will serve as model systems permitting unprecedented spatial and temporal resolution to help us better understand how the cell cycle is coordinated with various biological events.
从G1期到S期的细胞周期转变一直难以可视化。我们利用了标记细胞周期转变的反相振荡蛋白来开发用于此目的的基因编码荧光探针。这些探针有效地将单个G1期细胞核标记为红色,将处于S/G2/M期的细胞核标记为绿色。我们能够生成持续表达细胞周期探针的培养细胞和转基因小鼠,其中每个细胞核都呈现红色或绿色荧光。我们进行了延时成像,以探索培养细胞上皮-间质转化过程中、脑片中神经祖细胞的迁移和分化过程以及活体小鼠肿瘤跨血管生长过程中细胞周期动态的时空模式。这些小鼠和细胞系将作为模型系统,提供前所未有的空间和时间分辨率,以帮助我们更好地理解细胞周期如何与各种生物学事件协调。