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Cold stress-induced ferroptosis involves the ASK1-p38 pathway.
Hattori, Kazuki; Ishikawa, Hiroyuki; Sakauchi, Chihiro; Takayanagi, Saki; Naguro, Isao; Ichijo, Hidenori.
Afiliación
  • Hattori K; The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
  • Ishikawa H; The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
  • Sakauchi C; The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
  • Takayanagi S; The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
  • Naguro I; The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
  • Ichijo H; The Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan ichijo@mol.f.u-tokyo.ac.jp.
EMBO Rep ; 18(11): 2067-2078, 2017 11.
Article en En | MEDLINE | ID: mdl-28887319
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estrés Fisiológico / Apoptosis / MAP Quinasa Quinasa Quinasa 5 / Proteínas Quinasas p38 Activadas por Mitógenos / Hierro Límite: Humans Idioma: En Revista: EMBO Rep Asunto de la revista: BIOLOGIA MOLECULAR Año: 2017 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estrés Fisiológico / Apoptosis / MAP Quinasa Quinasa Quinasa 5 / Proteínas Quinasas p38 Activadas por Mitógenos / Hierro Límite: Humans Idioma: En Revista: EMBO Rep Asunto de la revista: BIOLOGIA MOLECULAR Año: 2017 Tipo del documento: Article País de afiliación: Japón