CD2AP at the junction of nephropathy and Alzheimer’s disease

IF 14.9 1区 医学 Q1 NEUROSCIENCES
Milene Vandal, Mohsen Janmaleki, Isabel Rea, Colin Gunn, Sotaro Hirai, Jeff Biernaskie, Justin Chun, Grant Gordon, Andrey Shaw, Amir Sanati-Nezhad, Gerald Pfeffer, Frederic Calon, Minh Dang Nguyen
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引用次数: 0

Abstract

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.
CD2AP在肾病和阿尔茨海默病的交界处
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,该基因的变异也会引起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基因剂量对AD关键病理特征的影响的细胞类型和机制。本文综述了CD2AP在哺乳动物细胞和系统中的基本作用,讨论了CD2AP在AD中的新发病机制,并强调了在CD2AP研究中纳入生物学性别的必要性。最后,文章在血管和分子组织的基础上得出了肾和脑生理学之间的重要相似之处,将肾脏疾病与AD联系起来,并提出AD中存在以CD2AP为中心的肾-脑轴。
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来源期刊
Molecular Neurodegeneration
Molecular Neurodegeneration 医学-神经科学
CiteScore
23.00
自引率
4.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Molecular Neurodegeneration, an open-access, peer-reviewed journal, comprehensively covers neurodegeneration research at the molecular and cellular levels. Neurodegenerative diseases, such as Alzheimer's, Parkinson's, Huntington's, and prion diseases, fall under its purview. These disorders, often linked to advanced aging and characterized by varying degrees of dementia, pose a significant public health concern with the growing aging population. Recent strides in understanding the molecular and cellular mechanisms of these neurodegenerative disorders offer valuable insights into their pathogenesis.
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