Department of Molecular Cell Biology and Immunology, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Front Immunol. 2021 Jan 29;11:620348. doi: 10.3389/fimmu.2020.620348. eCollection 2020.
Alzheimer's disease (AD) is the leading cause of dementia worldwide giving rise to devastating forms of cognitive decline, which impacts patients' lives and that of their proxies. Pathologically, AD is characterized by extracellular amyloid deposition, neurofibrillary tangles and chronic neuroinflammation. To date, there is no cure that prevents progression of AD. In this review, we elaborate on how bioactive lipids, including sphingolipids (SL) and specialized pro-resolving lipid mediators (SPM), affect ongoing neuroinflammatory processes during AD and how we may exploit them for the development of new biomarker panels and/or therapies. In particular, we here describe how SPM and SL metabolism, ranging from ω-3/6 polyunsaturated fatty acids and their metabolites to ceramides and sphingosine-1-phosphate, initiates pro- and anti-inflammatory signaling cascades in the central nervous system (CNS) and what changes occur therein during AD pathology. Finally, we discuss novel therapeutic approaches to resolve chronic neuroinflammation in AD by modulating the SPM and SL pathways.
阿尔茨海默病(AD)是全球范围内导致痴呆的主要原因,引发了严重的认知能力下降,影响了患者及其家属的生活。从病理上看,AD 的特征是细胞外淀粉样蛋白沉积、神经原纤维缠结和慢性神经炎症。迄今为止,尚无预防 AD 进展的方法。在这篇综述中,我们详细阐述了生物活性脂质,包括神经鞘脂(SL)和特殊的促解决脂质介质(SPM),如何影响 AD 期间持续的神经炎症过程,以及我们如何利用它们来开发新的生物标志物面板和/或治疗方法。特别是,我们在这里描述了 SPM 和 SL 代谢,从 ω-3/6 多不饱和脂肪酸及其代谢物到神经酰胺和鞘氨醇-1-磷酸,如何在中枢神经系统(CNS)中引发促炎和抗炎信号级联反应,以及 AD 病理过程中发生了哪些变化。最后,我们讨论了通过调节 SPM 和 SL 途径来解决 AD 中慢性神经炎症的新治疗方法。