School of Molecular Biosciences and Center for Reproductive Biology, Washington State University, Pullman, WA, USA.
Department of Biology, Stanford University, Stanford, CA, USA.
Dev Cell. 2020 Aug 24;54(4):447-454.e4. doi: 10.1016/j.devcel.2020.06.019. Epub 2020 Jul 10.
Dietary lipids impact development, homeostasis, and disease, but links between specific dietary fats and cell fates are poorly understood. Ferroptosis is an iron-dependent form of nonapoptotic cell death associated with oxidized polyunsaturated phospholipids. Here, we show that dietary ingestion of the polyunsaturated fatty acid (PUFA) dihomogamma-linolenic acid (DGLA; 20:3n-6) can trigger germ-cell ferroptosis and sterility in the nematode Caenorhabditis elegans. Exogenous DGLA is also sufficient to induce ferroptosis in human cells, pinpointing this omega-6 PUFA as a conserved metabolic instigator of this lethal process. In both C. elegans and human cancer cells, ether-lipid synthesis protects against ferroptosis. These results establish C. elegans as a powerful animal model to study the induction and modulation of ferroptosis by dietary fats and indicate that endogenous ether lipids act to prevent this nonapoptotic cell fate.
饮食中的脂质会影响细胞的发育、稳态和疾病,但人们对特定膳食脂肪与细胞命运之间的联系知之甚少。铁死亡是一种与氧化多不饱和磷脂有关的铁依赖性非凋亡性细胞死亡形式。在这里,我们表明,多不饱和脂肪酸(PUFA)二同型-γ-亚麻酸(DGLA;20:3n-6)的饮食摄入可以在秀丽隐杆线虫中引发生殖细胞铁死亡和不育。外源性 DGLA 也足以诱导人细胞发生铁死亡,这表明这种 ω-6 PUFA 是引发这一致命过程的保守代谢触发因素。在秀丽隐杆线虫和人类癌细胞中,醚脂合成可防止铁死亡。这些结果确立了秀丽隐杆线虫作为一种强大的动物模型,可用于研究膳食脂肪诱导和调节铁死亡的机制,并表明内源性醚脂可防止这种非凋亡性细胞命运。