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Necroptosis is preceded by nuclear translocation of the signaling proteins that induce it

机译:坏死性坏死是由信号转导蛋白引起的

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A signaling pathway that induces programmed necrotic cell death (necroptosis) was reported to be activated in cells by several cytokines and various pathogen components. The major proteins participating in that pathway are the protein kinases RIPK1 and RIPK3 and the pseudokinase mixed lineage kinase domain-like protein (MLKL). Recent studies have suggested that MLKL, once activated, mediates necroptosis by binding to cellular membranes, thereby triggering ion fluxes. However, our knowledge of both the sequence of molecular events leading to MLKL activation and the subcellular sites of these events is fragmentary. Here we report that the association of MLKL with the cell membrane in necroptotic death is preceded by the translocation of phosphorylated MLKL, along with RIPK1 and RIPK3, to the nucleus.
机译:据报道,一种诱导程序性坏死性细胞死亡(坏死性坏死病)的信号通路在细胞中被几种细胞因子和各种病原体成分​​激活。参与该途径的主要蛋白是蛋白激酶RIPK1和RIPK3以及假激酶混合谱系激酶结构域样蛋白(MLKL)。最近的研究表明,MLKL一旦被激活,就会通过与细胞膜结合而介导坏死病,从而触发离子通量。但是,我们对导致MLKL活化的分子事件序列和这些事件的亚细胞位点的知识都是零碎的。在这里,我们报道在尸检死亡中MLKL与细胞膜的结合是磷酸化MLKL以及RIPK1和RIPK3转运到细胞核之前。

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