Sanluca Chiara, Spagnolo Paolo, Mancinelli Romina, De Bartolo Maria Ilenia, Fava Marina, Maccarrone Mauro, Carotti Simone, Gaudio Eugenio, Leuti Alessandro, Vivacqua Giorgio
Department of Medicine, Laboratory of Microscopic and Ultrastructural Anatomy, Campus Bio-Medico University of Rome, Via Alvaro del Portillo 21, 00128 Rome, Italy.
Biochemistry and Molecular Biology Unit, Department of Medicine, Campus Bio-Medico University of Rome, Via Alvaro del Portillo 21, 00128 Rome, Italy.
Metabolites. 2024 Jun 22;14(7):352. doi: 10.3390/metabo14070352.
The present review provides a comprehensive examination of the intricate dynamics between α-synuclein, a protein crucially involved in the pathogenesis of several neurodegenerative diseases, including Parkinson's disease and multiple system atrophy, and endogenously-produced bioactive lipids, which play a pivotal role in neuroinflammation and neurodegeneration. The interaction of α-synuclein with bioactive lipids is emerging as a critical factor in the development and progression of neurodegenerative and neuroinflammatory diseases, offering new insights into disease mechanisms and novel perspectives in the identification of potential biomarkers and therapeutic targets. We delve into the molecular pathways through which α-synuclein interacts with biological membranes and bioactive lipids, influencing the aggregation of α-synuclein and triggering neuroinflammatory responses, highlighting the potential of bioactive lipids as biomarkers for early disease detection and progression monitoring. Moreover, we explore innovative therapeutic strategies aimed at modulating the interaction between α-synuclein and bioactive lipids, including the development of small molecules and nutritional interventions. Finally, the review addresses the significance of the gut-to-brain axis in mediating the effects of bioactive lipids on α-synuclein pathology and discusses the role of altered gut lipid metabolism and microbiota composition in neuroinflammation and neurodegeneration. The present review aims to underscore the potential of targeting α-synuclein-lipid interactions as a multifaceted approach for the detection and treatment of neurodegenerative and neuroinflammatory diseases.
本综述全面审视了α-突触核蛋白(一种在包括帕金森病和多系统萎缩在内的多种神经退行性疾病发病机制中起关键作用的蛋白质)与内源性产生的生物活性脂质之间复杂的动态关系,这些生物活性脂质在神经炎症和神经退行性变中起关键作用。α-突触核蛋白与生物活性脂质的相互作用正成为神经退行性和神经炎症性疾病发展和进展的关键因素,为疾病机制提供了新见解,并为潜在生物标志物和治疗靶点的识别提供了新视角。我们深入研究了α-突触核蛋白与生物膜和生物活性脂质相互作用的分子途径,这种相互作用影响α-突触核蛋白的聚集并引发神经炎症反应,突出了生物活性脂质作为疾病早期检测和进展监测生物标志物的潜力。此外,我们探索了旨在调节α-突触核蛋白与生物活性脂质相互作用的创新治疗策略,包括小分子的开发和营养干预。最后,本综述阐述了肠-脑轴在介导生物活性脂质对α-突触核蛋白病理影响方面的重要性,并讨论了肠道脂质代谢改变和微生物群组成在神经炎症和神经退行性变中的作用。本综述旨在强调靶向α-突触核蛋白-脂质相互作用作为检测和治疗神经退行性和神经炎症性疾病的多方面方法的潜力。