Venegas Carmen, Heneka Michael T
Department of Neurodegenerative Disease and Gerontopsychiatry, University of Bonn, Bonn, Germany; and.
Department of Neurodegenerative Disease and Gerontopsychiatry, University of Bonn, Bonn, Germany; and
J Leukoc Biol. 2017 Jan;101(1):87-98. doi: 10.1189/jlb.3MR0416-204R. Epub 2016 Oct 21.
Pathogen-associated molecular patterns (PAMPs) and endogenous "danger" signals, known as danger-associated molecular patterns (DAMPs), released from cells alert the innate immune system and activate several signal transduction pathways through interactions with the highly conserved pattern recognition receptors (PRRs). Both PAMPs and DAMPs directly induce proinflammatory cascades and trigger the formation of the inflammasome, mediating the release of cytokines. Here, we highlight the role of DAMPs, including amyloid β (Aβ), high-mobility group box 1 (HMGB1), the S100 family proteins, chromogranin A, and nucleic acids, in the innate-immune activation during the course of Alzheimer disease (AD), the most frequent neurodegenerative disorder.
病原体相关分子模式(PAMPs)和内源性“危险”信号,即所谓的危险相关分子模式(DAMPs),从细胞中释放出来,通过与高度保守的模式识别受体(PRRs)相互作用,提醒先天免疫系统并激活多种信号转导途径。PAMPs和DAMPs都直接诱导促炎级联反应并触发炎性小体的形成,介导细胞因子的释放。在这里,我们强调了DAMPs在阿尔茨海默病(AD)这一最常见的神经退行性疾病过程中的先天免疫激活中的作用,这些DAMPs包括β淀粉样蛋白(Aβ)、高迁移率族蛋白B1(HMGB1)、S100家族蛋白、嗜铬粒蛋白A和核酸。