1] Clinical Neuroscience, Department of Neurology, University of Bonn, Sigmund-Freud-Strasse 25, 53127 Bonn, Germany. [2] Department of Internal Medicine, University of Massachusetts, Worcester, Massachusetts 01605, USA. [3] German Center for Neurodegenerative Diseases (DZNE), Ludwig-Erhard-Allee 2, 53175 Bonn, Germany.
Clinical Neuroscience, Department of Neurology, University of Bonn, Sigmund-Freud-Strasse 25, 53127 Bonn, Germany.
Nat Rev Immunol. 2014 Jul;14(7):463-77. doi: 10.1038/nri3705.
The triggering of innate immune mechanisms is emerging as a crucial component of major neurodegenerative diseases. Microglia and other cell types in the brain can be activated in response to misfolded proteins or aberrantly localized nucleic acids. This diverts microglia from their physiological and beneficial functions, and leads to their sustained release of pro-inflammatory mediators. In this Review, we discuss how the activation of innate immune signalling pathways - in particular, the NOD-, LRR- and pyrin domain-containing 3 (NLRP3) inflammasome - by aberrant host proteins may be a common step in the development of diverse neurodegenerative disorders. During chronic activation of microglia, the sustained exposure of neurons to pro-inflammatory mediators can cause neuronal dysfunction and contribute to cell death. As chronic neuroinflammation is observed at relatively early stages of neurodegenerative disease, targeting the mechanisms that drive this process may be useful for diagnostic and therapeutic purposes.
先天免疫机制的触发正在成为主要神经退行性疾病的一个关键组成部分。大脑中的小胶质细胞和其他细胞类型可以响应错误折叠的蛋白质或异常定位的核酸而被激活。这使小胶质细胞偏离了它们的生理和有益功能,并导致它们持续释放促炎介质。在这篇综述中,我们讨论了先天免疫信号通路的激活——特别是 NOD、LRR 和 pyrin 结构域包含 3(NLRP3)炎性小体——是如何通过异常的宿主蛋白在多种神经退行性疾病的发展中可能是一个共同步骤。在小胶质细胞的慢性激活过程中,神经元持续暴露于促炎介质会导致神经元功能障碍并导致细胞死亡。由于慢性神经炎症在神经退行性疾病的相对早期阶段就已经观察到,因此针对驱动这一过程的机制可能对诊断和治疗具有重要意义。