Visualizing spatiotemporal dynamics of multicellular cell-cycle progression

被引:1589
作者
Sakaue-Sawano, Asako [1 ,3 ]
Kurokawa, Hiroshi [1 ,4 ]
Morimura, Toshifumi [2 ]
Hanyu, Aki [5 ]
Hama, Hiroshi [1 ]
Osawa, Hatsuki [1 ]
Kashiwagi, Saori [2 ]
Fukami, Kiyoko [4 ]
Miyata, Takaki [5 ,6 ]
Miyoshi, Hiroyuki [7 ]
Imamura, Takeshi
Ogawa, Masaharu [2 ]
Masai, Hisao [8 ]
Miyawaki, Atsushi [1 ,3 ]
机构
[1] RIKEN, Brain Sci Inst, Adv Technol Dev Grp, Lab Cell Funct & Dynam, Wako, Saitama 3510198, Japan
[2] RIKEN, Brain Sci Inst, Adv Technol Dev Grp, Lab Cell Culture Dev, Wako, Saitama 3510198, Japan
[3] JST, ERATO, Wako, Saitama 3510198, Japan
[4] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Tokyo 1920392, Japan
[5] Japanese Fdn Canc Res, Inst Canc, Dept Biochem, Koto Ku, Tokyo 1358550, Japan
[6] Nagoya Univ, Grad Sch Med, Dept Anat & Cell Biol, Syowa Ku, Aichi 4668550, Japan
[7] RIKEN Tsukuba Inst, BioResource Ctr, Subteam Manipulat Cell Fate, Tsukuba, Ibaraki 3050074, Japan
[8] Tokyo Metropolitan Inst Med Sci, Gen Dynam Project, Bunkyo Ku, Tokyo 1138613, Japan
关键词
D O I
10.1016/j.cell.2007.12.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cell-cycle transition from G(1) 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 G, phase nuclei red and those in S/G(2)/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.
引用
收藏
页码:487 / 498
页数:12
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