小胶质细胞
脂质代谢
脂滴
嘌呤能受体
生物
基因型
载脂蛋白E
新陈代谢
神经科学
阿尔茨海默病
疾病
细胞生物学
医学
免疫学
病理
内分泌学
炎症
基因
生物化学
细胞外
作者
Xiqi Hu,Yanan Ma,Ying Xia
出处
期刊:BioScience Trends
[International Research and Cooperation Association for Bio & Socio-Sciences Advancement]
日期:2024-04-16
卷期号:18 (2): 195-197
被引量:26
标识
DOI:10.5582/bst.2024.01092
摘要
APOE4 is widely recognized as a genetic risk factor for Alzheimer's disease (AD), implicated in 60-80% of all AD cases. Recent research suggests that microglia carrying the APOE4 genotype display abnormal lipid metabolism and accumulate lipid droplets, which may exacerbate the pathology of AD. Microglia play a critical role in immune surveillance within the central nervous system and are responsible for removing harmful particles and preserving neuronal function. The APOE4 genotype causes abnormal lipid metabolism in microglia, resulting in excessive accumulation of lipid droplets. This accumulation not only impairs the phagocytic and clearance capabilities of microglia but also disrupts their interactions with neurons, resulting in disorganization and neurodegenerative alterations at the neuronal network level. In addition, the presence of APOE4 modifies the metabolic landscape of microglia, particularly affecting purinergic signaling and lipid metabolism, thereby exacerbating the pathological processes of AD. In conclusion, the accumulation of lipid droplets and abnormal lipid metabolism may be critical mechanisms in the progression of AD in microglia carrying the APOE4 genotype.
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