ANGPTL4 介导的小胶质细胞脂滴聚集:连接阿尔茨海默病和肥胖症的桥梁

IF 5.1 2区 医学 Q1 NEUROSCIENCES Neurobiology of Disease Pub Date : 2024-11-20 DOI:10.1016/j.nbd.2024.106741
Nan Li, Xiaojun Wang, Ruilang Lin, Fuxia Yang, Hung-Chen Chang, Xuchao Gu, Jun Shu, Guidong Liu, Yongfu Yu, Wenshi Wei, Zhijun Bao
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引用次数: 0

摘要

越来越多的证据表明,肥胖等代谢紊乱与阿尔茨海默病(AD)的发病有关。小胶质细胞中脂类的病理堆积被认为是大脑衰老和阿尔茨海默病进展的一个关键指标,但这一过程背后的机制仍不确定。脂肪因子 ANGPTL4 与肥胖密切相关,被认为在神经退行性疾病的发展过程中扮演了重要角色。本研究利用 RNA 测序确定了脂质蓄积的 BV2 小胶质细胞中的差异表达,并通过 ANGPTL4 在 BV2 中的过表达研究了其潜在机制。随后,研究人员利用动物模型和临床数据进一步探讨了AD中循环ANGPTL4水平的变化。RNA 测序结果表明,ANGPTL4 与小胶质细胞脂质积累之间存在相关性。在小胶质细胞中过表达 ANGPTL4 会导致炎症因子分泌增加、氧化应激水平升高和抗病毒能力减弱。此外,在体外用淀粉样β 1-42肽(Aβ)和游离脂肪酸(FFA)联合处理模拟AD和肥胖并存的情况时,我们观察到ANGPTL4的表达明显上调,这突显了它在AD和肥胖之间相互作用中的潜在作用。在体内实验中,与野生型对照组相比,我们还观察到 APP/PS1 小鼠海马和血浆中 ANGPTL4 的表达显著增加。与此同时,海马中的小胶质细胞活化增强,与长寿相关的基因表达减少。英国生物库的临床数据表明,与健康对照组相比,AD 患者的血浆 ANGPTL4 水平升高。此外,肥胖的AD患者的ANGPTL4水平明显高于非肥胖患者。我们的研究结果表明,ANGPTL4介导的小胶质细胞老化可能是AD与肥胖之间的关键环节,并提出将ANGPTL4作为AD的潜在生物标志物。
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ANGPTL4-mediated microglial lipid droplet accumulation: Bridging Alzheimer's disease and obesity.

Increasing evidence suggests that metabolic disorders such as obesity are implicated in the development of Alzheimer's disease (AD). The pathological buildup of lipids in microglia is regarded as a key indicator in brain aging and the progression of AD, yet the mechanisms behind this process remain uncertain. The adipokine ANGPTL4 is strongly associated with obesity and is thought to play a role in the advancement of neurodegenerative diseases. This study utilized RNA sequencing to identify differential expression in lipid-accumulating BV2 microglia and investigated the potential mechanism through ANGPTL4 overexpression in BV2. Subsequently, animal models and clinical data were employed to further explore alterations in circulating ANGPTL4 levels in AD. RNA sequencing results indicated a correlation between ANGPTL4 and microglial lipid accumulation. The overexpression of ANGPTL4 in microglia resulted in increased secretion of inflammatory factors, elevated oxidative stress levels, and diminished antiviral capacity. Furthermore, when simulating the coexistence of AD and obesity through combined treatment with Amyloid-Beta 1-42 peptide (Aβ) and Free Fatty Acids (FFA) in vitro, we observed a notable upregulation of ANGPTL4 expression, highlighting its potential role in the interplay between AD and obesity. In vivo experiments, we also observed a significant increase in ANGPTL4 expression in the hippocampus and plasma of APP/PS1 mice compared to wild-type controls. This was accompanied by heightened microglial activation and reduced expression of longevity-related genes in the hippocampus. Clinical data from the UK Biobank indicated that plasma ANGPTL4 levels are elevated in patients with AD when compared to healthy controls. Moreover, significantly higher ANGPTL4 levels were observed in obese AD patients relative to their non-obese counterparts. Our findings suggest that ANGPTL4-mediated microglial aging may serve as a crucial link between AD and obesity, proposing ANGPTL4 as a potential biomarker for AD.

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来源期刊
Neurobiology of Disease
Neurobiology of Disease 医学-神经科学
CiteScore
11.20
自引率
3.30%
发文量
270
审稿时长
76 days
期刊介绍: Neurobiology of Disease is a major international journal at the interface between basic and clinical neuroscience. The journal provides a forum for the publication of top quality research papers on: molecular and cellular definitions of disease mechanisms, the neural systems and underpinning behavioral disorders, the genetics of inherited neurological and psychiatric diseases, nervous system aging, and findings relevant to the development of new therapies.
期刊最新文献
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