组学
生物
蛋白质组学
表观遗传学
疾病
代谢组学
神经科学
计算生物学
基因组学
小胶质细胞
痴呆
转录组
生物信息学
病理
基因组
医学
DNA甲基化
遗传学
炎症
免疫学
基因
基因表达
作者
Özkan İş,Yuhao Min,Xue Wang,Stephanie R. Oatman,Ann Abraham Daniel,Nilüfer Ertekin‐Taner
出处
期刊:Glia
[Wiley]
日期:2024-12-09
摘要
ABSTRACT Alzheimer's disease (AD) is the most common neurodegenerative dementia with multi‐layered complexity in its molecular etiology. Multiple omics‐based approaches, such as genomics, epigenomics, transcriptomics, proteomics, metabolomics, and lipidomics are enabling researchers to dissect this molecular complexity, and to uncover a plethora of alterations yielding insights into the pathophysiology of this disease. These approaches reveal multi‐omics alterations essentially in all cell types of the brain, including glia. In this systematic review, we screen the literature for human studies implementing any omics approach within the last 10 years, to discover AD‐associated molecular perturbations in brain glial cells. The findings from over 200 AD‐related studies are reviewed under four different glial cell categories: microglia, oligodendrocytes, astrocytes and brain vascular cells. Under each category, we summarize the shared and unique molecular alterations identified in glial cells through complementary omics approaches. We discuss the implications of these findings for the development, progression and ultimately treatment of this complex disease as well as directions for future omics studies in glia cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI