Department of Biological Sciences, University of Limerick, Limerick, V94PH61, Ireland.
Bernal Institute, University of Limerick, Analog Devices Building AD3-018, Castletroy, Limerick, V94PH61, Ireland.
Lipids Health Dis. 2024 Apr 20;23(1):113. doi: 10.1186/s12944-024-02106-z.
Pro-inflammatory processes triggered by the accumulation of extracellular amyloid beta (Aβ) peptides are a well-described pathology in Alzheimer's disease (AD). Activated astrocytes surrounding Aβ plaques contribute to inflammation by secreting proinflammatory factors. While astrocytes may phagocytize Aβ and contribute to Aβ clearance, reactive astrocytes may also increase Aβ production. Therefore, identifying factors that can attenuate astrocyte activation and neuroinflammation and how these factors influence pro-inflammatory pathways is important for developing therapeutic and preventive strategies in AD. Here, we identify the platelet-activating factor receptor (PTAFR) pathway as a key mediator of astrocyte activation. Intriguingly, several polar lipids (PLs) have exhibited anti-inflammatory protective properties outside the central nervous system through their inhibitory effect on the PTAFR pathway. Thus, we additionally investigated whether different PLs also exert inhibitory effects on the PAF pathway in astrocytes and whether their presence influences astrocytic pro-inflammatory signaling and known AD pathologies in vitro.
PLs from salmon and yogurt were extracted using novel food-grade techniques and their fatty acid profile was determined using LC/MS. The effect of PLs on parameters such as astrocyte activation and generation of oxygen species (ROS) was assessed. Additionally, effects of the secretome of astrocytes treated with these polar lipids on aged neurons was measured.
We show that PLs obtained from salmon and yogurt lower astrocyte activation, the generation of reactive oxygen species (ROS), and extracellular Aβ accumulation. Cell health of neurons exposed to the secretome of astrocytes treated with salmon-derived PLs and Aβ was less affected than those treated with astrocytes exposed to Aβ only.
Our results highlight a novel underlying mechanism, why consuming PL-rich foods such as fish and dairy may reduce the risk of developing dementia and associated disorders.
细胞外淀粉样β (Aβ) 肽的积累引发的促炎过程是阿尔茨海默病 (AD) 的一种典型病理学。围绕 Aβ 斑块的活化星形胶质细胞通过分泌促炎因子促进炎症。虽然星形胶质细胞可以吞噬 Aβ 并有助于 Aβ 清除,但反应性星形胶质细胞也可能增加 Aβ 的产生。因此,确定可以减弱星形胶质细胞活化和神经炎症的因素以及这些因素如何影响促炎途径,对于开发 AD 的治疗和预防策略非常重要。在这里,我们确定血小板激活因子受体 (PTAFR) 途径是星形胶质细胞活化的关键介质。有趣的是,几种极性脂质 (PL) 通过其对 PTAFR 途径的抑制作用,在中枢神经系统外表现出抗炎保护特性。因此,我们还研究了不同的 PL 是否也对星形胶质细胞中的 PAF 途径发挥抑制作用,以及它们的存在是否会影响体外星形胶质细胞的促炎信号和已知的 AD 病理。
使用新型食品级技术从三文鱼和酸奶中提取 PL,并使用 LC/MS 测定其脂肪酸谱。评估 PL 对星形胶质细胞活化和氧物种 (ROS) 生成等参数的影响。此外,还测量了用这些极性脂质处理的星形胶质细胞的分泌产物对老年神经元的影响。
我们表明,从三文鱼和酸奶中获得的 PL 可降低星形胶质细胞的活化、活性氧 (ROS) 的产生和细胞外 Aβ 的积累。与仅用 Aβ 处理的星形胶质细胞相比,暴露于用三文鱼衍生的 PL 处理的星形胶质细胞的 secretome 的神经元的细胞健康受到的影响较小。
我们的研究结果强调了一种新的潜在机制,即食用富含 PL 的食物(如鱼类和乳制品)可能降低患痴呆症和相关疾病的风险的原因。