Leri Manuela, Vasarri Marzia, Carnemolla Federica, Oriente Francesco, Cabaro Serena, Stio Maria, Degl'Innocenti Donatella, Stefani Massimo, Bucciantini Monica
Dipartimento di Scienze Biomediche Sperimentali e Cliniche "Mario Serio", Università degli Studi di Firenze, 50134 Firenze, Italy.
Dipartimento di Scienze Mediche Traslazionali, Università di Napoli Federico II, 80138 Napoli, Italy.
Pharmaceuticals (Basel). 2023 Jun 27;16(7):933. doi: 10.3390/ph16070933.
In Alzheimer's disease (AD), microglia, brain resident immune cells, become chronically inflammatory and neurotoxic. In recent years, neuroinflammation has attracted particular interest in the scientific community. The genetic variants of molecules associated with ''microgliopathies'', including the triggering receptor expressed in myeloid cells-2 (TREM2), result in increased risk of developing AD and cognitive decline. We performed a set of in vitro assays using human neuronal (SH-SY5Y) and microglial (BV2 and C13NJ) cell models. Cells were differentially treated with extra virgin olive oil (EVOO) polyphenols, oleuropein aglycone (OleA) and hydroxytyrosol (HT) before adding LPS. We evaluated the protective effects of these EVOO products by a set of biochemical and cell biology assays, including ELISA, MTT, ROS detection, Western blotting and immunofluorescence. Our results provide an integrated understanding of the neuroprotection exerted by polyphenols in terms of: (i) reduction of pro-inflammatory cytokines release (IL-6, IL-8, IP-10 and RANTES); (ii) activation of the TREM2-dependent anti-inflammatory pathway; (iii) enhancement of protective microglial activity favoring the M2 polarization phenotype. Such findings provide new and important insights into the mechanisms by which the dietary olive polyphenols exert beneficial properties against neuroinflammation and neuronal impairment.
在阿尔茨海默病(AD)中,小胶质细胞作为脑内常驻免疫细胞会发生慢性炎症反应并产生神经毒性。近年来,神经炎症引起了科学界的特别关注。与“小胶质细胞病变”相关分子的基因变异,包括髓样细胞表达的触发受体2(TREM2),会增加患AD和认知衰退的风险。我们使用人类神经元(SH-SY5Y)和小胶质细胞(BV2和C13NJ)细胞模型进行了一系列体外试验。在添加脂多糖(LPS)之前,用特级初榨橄榄油(EVOO)多酚、橄榄苦苷配基(OleA)和羟基酪醇(HT)对细胞进行不同处理。我们通过一系列生化和细胞生物学试验评估了这些EVOO产品的保护作用,包括酶联免疫吸附测定(ELISA)、噻唑蓝(MTT)、活性氧(ROS)检测、蛋白质免疫印迹法(Western blotting)和免疫荧光法。我们的结果从以下几个方面提供了对多酚神经保护作用的综合理解:(i)减少促炎细胞因子的释放(白细胞介素-6、白细胞介素-8、干扰素γ诱导蛋白10和调节激活正常T细胞表达和分泌因子);(ii)激活TREM2依赖性抗炎途径;(iii)增强有利于M2极化表型的保护性小胶质细胞活性。这些发现为膳食橄榄多酚对神经炎症和神经元损伤发挥有益作用的机制提供了新的重要见解。