Chen Yu-Lin, Reddy Syon, Suzuki Aussie
McArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Molecular and Cellular Pharmacology Graduate Program, University of Wisconsin-Madison, Madison, Wisconsin, USA.
bioRxiv. 2024 Sep 3:2024.09.02.610832. doi: 10.1101/2024.09.02.610832.
The cell cycle is a crucial process for cell proliferation, differentiation, and development. Numerous genes and proteins play pivotal roles at specific cell cycle stages to regulate these events precisely. Studying the stage-specific functions of the cell cycle requires accumulating cell populations at the desired cell cycle stage. Cell synchronization, achieved through the use of cell cycle kinase and protein inhibitors, is often employed for this purpose. However, suboptimal concentrations of these inhibitors can result in reduced efficiency, irreversibility, and undesirable cell cycle defects. In this study, we have optimized effective and reversible techniques to synchronize the cell cycle at each stage in human RPE1 cells, utilizing both fixed high-precision cell cycle identification methods and high-temporal live-cell imaging. These reproducible synchronization methods are invaluable for investigating the regulatory mechanisms specific to each cell cycle stage.
细胞周期是细胞增殖、分化和发育的关键过程。众多基因和蛋白质在特定的细胞周期阶段发挥关键作用,以精确调节这些事件。研究细胞周期的阶段特异性功能需要在所需的细胞周期阶段积累细胞群体。为此,通常采用通过使用细胞周期激酶和蛋白质抑制剂实现的细胞同步化方法。然而,这些抑制剂的浓度不合适会导致效率降低、不可逆性以及不良的细胞周期缺陷。在本研究中,我们利用固定的高精度细胞周期识别方法和高时间分辨率的活细胞成像技术,优化了在人RPE1细胞的每个阶段同步细胞周期的有效且可逆的技术。这些可重复的同步方法对于研究每个细胞周期阶段特有的调控机制非常宝贵。