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Necroptosis and RIPK1-mediated neuroinflammation in CNS diseases

机译:中枢神经系统疾病中的虐疮和ripk1介导的神经炎炎症

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Apoptosis is crucial for the normal development of the nervous system, whereas neurons in the adult CNS are relatively resistant to this form of cell death. However, under pathological conditions, upregulation of death receptor family ligands, such as tumour necrosis factor (TNF), can sensitize cells in the CNS to apoptosis and a form of regulated necrotic cell death known as necroptosis that is mediated by receptor-interacting protein kinase 1 (RIPK1), RIPK3 and mixed lineage kinase domain-like protein (MLKL). Necroptosis promotes further cell death and neuroinflammation in the pathogenesis of several neurodegenerative diseases, including multiple sclerosis, amyotrophic lateral sclerosis, Parkinson disease and Alzheimer disease. In this Review, we outline the evidence implicating necroptosis in these neurological diseases and suggest that targeting RIPK1 might help to inhibit multiple cell death pathways and ameliorate neuroinflammation.
机译:细胞凋亡对于神经系统的正常发育至关重要,而成年CNS中的神经元对这种形式的细胞死亡是相对抗性的。 然而,在病理条件下,死亡受体家族配体的上调,例如肿瘤坏死因子(TNF),可以敏感CNS中的细胞以凋亡,并且一种被称为Necroptis的受调节的坏死性细胞死亡的形式是由受体 - 相互作用的蛋白激酶介导的 1(RIPK1),RIPK3和混合谱系激酶域样蛋白(MLK1)。 Necroptis促进了几种神经变性疾病的发病机制中的进一步细胞死亡和神经炎症,包括多发性硬化症,肌萎缩侧面硬化,帕金森病和阿尔茨海默病。 在这篇综述中,我们概述了暗示这种神经疾病中肮脏病的证据,并表明靶向ripk1可能有助于抑制多种细胞死亡途径和改善神经炎症。

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