Hamann Jens C, Surcel Alexandra, Chen Ruoyao, Teragawa Carolyn, Albeck John G, Robinson Douglas N, Overholtzer Michael
Cell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Louis V. Gerstner, Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Cell Rep. 2017 Jul 5;20(1):201-210. doi: 10.1016/j.celrep.2017.06.037.
Entosis is a mechanism of cell death that involves neighbor cell ingestion. This process occurs in cancers and promotes a form of cell competition, where winner cells engulf and kill losers. Entosis is driven by a mechanical differential that allows softer cells to eliminate stiffer cells. While this process can be induced by matrix detachment, whether other stressors can activate entosis is unknown. Here, we find that entosis is induced in adherent cells by glucose withdrawal. Glucose withdrawal leads to a bimodal distribution of cells based on their deformability, where stiffer cells appear in a manner requiring the energy-sensing AMP-activated protein kinase (AMPK). We show that loser cells with high levels of AMPK activity are eliminated by winners through entosis, which supports winner cell proliferation under nutrient-deprived conditions. Our findings demonstrate that entosis serves as a cellular response to metabolic stress that enables nutrient recovery through neighbor cell ingestion.
细胞内吞是一种涉及邻近细胞吞噬的细胞死亡机制。这一过程发生在癌症中,并促进一种细胞竞争形式,即获胜细胞吞噬并杀死失败细胞。细胞内吞由机械差异驱动,使较软的细胞能够清除较硬的细胞。虽然这一过程可由基质脱离诱导,但其他应激源是否能激活细胞内吞尚不清楚。在这里,我们发现葡萄糖剥夺可诱导贴壁细胞发生细胞内吞。葡萄糖剥夺导致细胞根据其变形能力出现双峰分布,其中较硬的细胞以一种需要能量感应的AMP激活蛋白激酶(AMPK)的方式出现。我们表明,具有高水平AMPK活性的失败细胞会被获胜细胞通过细胞内吞清除,这支持了营养缺乏条件下获胜细胞的增殖。我们的研究结果表明,细胞内吞作为一种对代谢应激的细胞反应,能够通过邻近细胞吞噬实现营养恢复。