Department of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.
Elife. 2020 Apr 29;9:e54565. doi: 10.7554/eLife.54565.
Tetraploidy has long been of interest to both cell and cancer biologists, partly because of its documented role in tumorigenesis. A common model proposes that the extra centrosomes that are typically acquired during tetraploidization are responsible for driving tumorigenesis. However, tetraploid cells evolved in culture have been shown to lack extra centrosomes. This observation raises questions about how tetraploid cells evolve and more specifically about the mechanisms(s) underlying centrosome loss. Here, using a combination of fixed cell analysis, live cell imaging, and mathematical modeling, we show that populations of newly formed tetraploid cells rapidly evolve in vitro to retain a near-tetraploid chromosome number while losing the extra centrosomes gained at the time of tetraploidization. This appears to happen through a process of natural selection in which tetraploid cells that inherit a single centrosome during a bipolar division with asymmetric centrosome clustering are favored for long-term survival.
四倍体一直引起细胞和癌症生物学家的兴趣,部分原因是它在肿瘤发生中的作用已有文献记载。一个常见的模型提出,在四倍体化过程中通常获得的额外中心体负责驱动肿瘤发生。然而,已经表明在培养中进化的四倍体细胞缺乏额外的中心体。这一观察结果引发了关于四倍体细胞如何进化的问题,更具体地说,是关于中心体丢失的机制。在这里,我们使用固定细胞分析、活细胞成像和数学建模的组合,表明新形成的四倍体细胞群体在体外迅速进化,以保持接近四倍体的染色体数量,同时失去在四倍体化时获得的额外中心体。这似乎是通过一种自然选择的过程发生的,其中在具有不对称中心体聚集的两极分裂过程中遗传单个中心体的四倍体细胞有利于长期存活。