The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan
EMBO Rep. 2017 Nov;18(11):2067-2078. doi: 10.15252/embr.201744228. Epub 2017 Sep 8.
A wide variety of cell death mechanisms, such as ferroptosis, have been proposed in mammalian cells, and the classification of cell death attracts global attention because each type of cell death has the potential to play causative roles in specific diseases. However, the precise molecular mechanisms leading to cell death are poorly understood, particularly in ferroptosis. Here, we show that continuous severe cold stress induces ferroptosis and the ASK1-p38 MAPK pathway in multiple cell lines. The activation of the ASK1-p38 pathway is mediated by critical determinants of ferroptosis: MEK activity, iron ions, and lipid peroxide. The chemical compound erastin, a potent ferroptosis inducer, also activates the ASK1-p38 axis downstream of lipid peroxide accumulation and leads to ASK1-dependent cell death in a cell type-specific manner. These lines of evidence provide mechanistic insight into ferroptosis, a type of regulated necrosis.
多种细胞死亡机制,如铁死亡,在哺乳动物细胞中被提出,细胞死亡的分类引起了全球关注,因为每种类型的细胞死亡都有可能在特定疾病中起因果作用。然而,导致细胞死亡的确切分子机制尚不清楚,特别是在铁死亡中。在这里,我们表明持续的严重冷应激诱导多种细胞系中的铁死亡和 ASK1-p38 MAPK 途径。ASK1-p38 途径的激活是由铁死亡的关键决定因素介导的:MEK 活性、铁离子和脂质过氧化物。化学化合物 erastin,一种有效的铁死亡诱导剂,也在脂质过氧化物积累的下游激活 ASK1-p38 轴,并导致 ASK1 依赖性细胞死亡,具有细胞类型特异性。这些证据为一种受调控的坏死形式的铁死亡提供了机制上的见解。