İş Özkan, Min Yuhao, Wang Xue, Oatman Stephanie R, Abraham Daniel Ann, Ertekin-Taner Nilüfer
Department of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA.
Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, Florida, USA.
Glia. 2025 Mar;73(3):539-573. doi: 10.1002/glia.24652. Epub 2024 Dec 9.
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.
阿尔茨海默病(AD)是最常见的神经退行性痴呆,其分子病因具有多层次的复杂性。基于多种组学的方法,如基因组学、表观基因组学、转录组学、蛋白质组学、代谢组学和脂质组学,使研究人员能够剖析这种分子复杂性,并揭示大量改变,从而深入了解该疾病的病理生理学。这些方法揭示了大脑所有细胞类型(包括神经胶质细胞)中本质上的多组学改变。在本系统评价中,我们筛选了过去10年内采用任何组学方法的人体研究文献,以发现脑胶质细胞中与AD相关的分子扰动。来自200多项与AD相关研究的结果在四种不同的神经胶质细胞类别下进行综述:小胶质细胞、少突胶质细胞、星形胶质细胞和脑血管细胞。在每个类别下,我们总结了通过互补组学方法在胶质细胞中鉴定出的共同和独特的分子改变。我们讨论了这些发现对这种复杂疾病的发生、发展以及最终治疗的意义,以及未来胶质细胞组学研究的方向。