Entosis is a form of epithelial cell cannibalism that is prevalent in human cancer, typically triggered by loss of matrix adhesion. Here, we report an alternative mechanism for entosis in human epithelial cells, driven by mitosis. Mitotic entosis is regulated by Cdc42, which controls mitotic morphology. Cdc42 depletion enhances mitotic deadhesion and rounding, and these biophysical changes, which depend on RhoA activation and are phenocopied by Rap1 inhibition, permit subsequent entosis. Mitotic entosis occurs constitutively in some human cancer cell lines and mitotic index correlates with cell cannibalism in primary human breast tumours. Adherent, wild-type cells can act efficiently as entotic hosts, suggesting that normal epithelia may engulf and kill aberrantly dividing neighbours. Finally, we report that Paclitaxel/taxol promotes mitotic rounding and subsequent entosis, revealing an unconventional activity of this drug. Together, our data uncover an intriguing link between cell division and cannibalism, of significance to both cancer and chemotherapy.
Mitosis can drive cell cannibalism through entosis.
有丝分裂可以通过胞吞作用驱动细胞自相残杀
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作者:Durgan Joanne, Tseng Yun-Yu, Hamann Jens C, Domart Marie-Charlotte, Collinson Lucy, Hall Alan, Overholtzer Michael, Florey Oliver
| 期刊: | Elife | 影响因子: | 6.400 |
| 时间: | 2017 | 起止号: | 2017 Jul 11; 6:e27134 |
| doi: | 10.7554/eLife.27134 | 研究方向: | 细胞生物学 |
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