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细胞坏死和 RIPK1 介导的中枢神经系统疾病中的神经炎症。

Necroptosis and RIPK1-mediated neuroinflammation in CNS diseases.

机构信息

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Neuroscience Research, Sanofi, Framingham, MA, USA.

出版信息

Nat Rev Neurosci. 2019 Jan;20(1):19-33. doi: 10.1038/s41583-018-0093-1.

Abstract

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.

摘要

细胞凋亡对于神经系统的正常发育至关重要,而成年中枢神经系统中的神经元对此种细胞死亡形式具有较强的抵抗力。然而,在病理条件下,死亡受体家族配体(如肿瘤坏死因子(TNF))的上调可使中枢神经系统中的细胞对细胞凋亡和一种称为坏死性细胞死亡的受调控的坏死形式(由受体相互作用蛋白激酶 1(RIPK1)、RIPK3 和混合谱系激酶结构域样蛋白(MLKL)介导)敏感。坏死性细胞死亡促进了几种神经退行性疾病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、肌萎缩侧索硬化症、帕金森病和阿尔茨海默病。在本综述中,我们概述了坏死性细胞死亡与这些神经疾病的关联证据,并提出了靶向 RIPK1 可能有助于抑制多种细胞死亡途径和改善神经炎症的观点。

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