Vandal Milene, Janmaleki Mohsen, Rea Isabel, Gunn Colin, Hirai Sotaro, Biernaskie Jeff, Chun Justin, Gordon Grant, Shaw Andrey, Sanati-Nezhad Amir, Pfeffer Gerald, Calon Frederic, Nguyen Minh Dang
Department of Clinical Neurosciences, Hotchkiss Brain Institute, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Department of Cell Biology and Anatomy, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Mol Neurodegener. 2025 Jun 4;20(1):63. doi: 10.1186/s13024-025-00852-x.
Polymorphisms in the gene encoding CD2-associated protein (CD2AP) are associated with an increased risk for developing Alzheimer's disease (AD). Intriguingly, variants in the gene also cause a pattern of kidney injury termed focal segmental glomerulosclerosis. Recent studies have investigated the cell types and mechanisms by which CD2AP gene dosage contributes to the key pathological features of AD. This review summarizes the fundamental roles of CD2AP in mammalian cells and systems, discusses the novel pathogenic mechanisms focused on CD2AP in AD and highlights the necessity of incorporating biological sex in CD2AP research. Finally, the article draws important parallels between kidney and brain physiology based on vascular and molecular organization, links kidney disease to AD, and suggests the existence of a kidney-brain axis in AD centered on CD2AP.
编码CD2相关蛋白(CD2AP)的基因多态性与患阿尔茨海默病(AD)的风险增加有关。有趣的是,该基因的变异还会导致一种称为局灶节段性肾小球硬化的肾损伤模式。最近的研究调查了CD2AP基因剂量导致AD关键病理特征的细胞类型和机制。本综述总结了CD2AP在哺乳动物细胞和系统中的基本作用,讨论了AD中以CD2AP为重点的新致病机制,并强调了在CD2AP研究中纳入生物性别的必要性。最后,本文基于血管和分子组织在肾脏和大脑生理学之间得出重要的相似之处,将肾脏疾病与AD联系起来,并提出以CD2AP为中心的AD中存在肾-脑轴。