Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.
Johns Hopkins School of Medicine, Baltimore, MD, USA.
Methods Mol Biol. 2022;2579:99-110. doi: 10.1007/978-1-0716-2736-5_8.
The cell cycle is a series of events leading to cell replication. When plated at low cell densities in serum-containing medium, cultured cells start to proliferate, moving through the four phases of the cell cycle: G1, S, G2, and M. Mitosis is the most dynamic period of the cell cycle, involving a major reorganization of virtually all cell components. Mitosis is further divided into prophase, prometaphase, metaphase, anaphase, and telophase, which can be easily distinguished from one another by protein markers and/or comparing their chromosome morphology under fluorescence microscope. The progression of the cell cycle through these mitotic subphases is tightly regulated by complicated molecular mechanisms. Synchronization of cells to the mitotic subphases is important for understanding these molecular mechanisms. Here, we describe a protocol to synchronize Hela cells to prometaphase, metaphase, and anaphase/telophase. In this protocol, Hela cells are first synchronized to the early S phase by a double thymidine block. Following the release of the block, the cells are treated with nocodazole, MG132, and blebbistatin to arrest them at prometaphase, metaphase, and anaphase/telophase, respectively. Successful synchronization is assessed using Western blot and fluorescence microscopy.
细胞周期是一系列导致细胞复制的事件。当在含有血清的培养基中以低细胞密度接种时,培养的细胞开始增殖,经历细胞周期的四个阶段:G1、S、G2 和 M。有丝分裂是细胞周期中最具活力的阶段,涉及到几乎所有细胞成分的重大重组。有丝分裂进一步分为前期、前中期、中期、后期和末期,可以通过蛋白质标记物或在荧光显微镜下比较其染色体形态轻松区分。细胞周期通过这些有丝分裂亚期的进展受到复杂的分子机制的严格调控。细胞同步到有丝分裂亚期对于理解这些分子机制非常重要。在这里,我们描述了一种将 Hela 细胞同步到前期、中期和后期/末期的方案。在该方案中,Hela 细胞首先通过双重胸苷阻断被同步到早期 S 期。阻断释放后,用诺考达唑、MG132 和 blebbistatin 处理细胞,分别将其阻滞在前期、中期和后期/末期。使用 Western blot 和荧光显微镜评估同步是否成功。