小胶质细胞
生物
传出细胞增多
基因
疾病
功能基因组学
阿尔茨海默病
遗传学
神经退行性变
梅尔特克
全基因组关联研究
基因组学
神经科学
巨噬细胞
基因组
免疫学
炎症
医学
信号转导
病理
单核苷酸多态性
基因型
受体酪氨酸激酶
体外
作者
Carmen Romero‐Molina,Francesca Garretti,Shea J. Andrews,Edoardo Marcora,Alison Goate
出处
期刊:Neuron
[Elsevier]
日期:2022-11-01
卷期号:110 (21): 3513-3533
被引量:43
标识
DOI:10.1016/j.neuron.2022.10.015
摘要
Genome-wide association studies and functional genomics studies have linked specific cell types, genes, and pathways to Alzheimer’s disease (AD) risk. In particular, AD risk alleles primarily affect the abundance or structure, and thus the activity, of genes expressed in macrophages, strongly implicating microglia (the brain-resident macrophages) in the etiology of AD. These genes converge on pathways (endocytosis/phagocytosis, cholesterol metabolism, and immune response) with critical roles in core macrophage functions such as efferocytosis. Here, we review these pathways, highlighting relevant genes identified in the latest AD genetics and genomics studies, and describe how they may contribute to AD pathogenesis. Investigating the functional impact of AD-associated variants and genes in microglia is essential for elucidating disease risk mechanisms and developing effective therapeutic approaches.
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