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阿尔茨海默病中细胞外囊泡的蛋白质组学特征分析:全面综述

Proteomics profiling of extracellular vesicle for identification of potential biomarkers in Alzheimer's disease: A comprehensive review.

机构信息

Qinba State Key Laboratory of Biological Resources and Ecological Environment, 2011 QinLing-Bashan Mountains Bioresources Comprehensive Development C. I. C, Shaanxi Province Key Laboratory of Bio-Resources, College of Bioscience and Bioengineering, Shaanxi University of Technology, Hanzhong 723001, China.

Department of Chemical Technology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

Ageing Res Rev. 2024 Aug;99:102359. doi: 10.1016/j.arr.2024.102359. Epub 2024 May 29.

Abstract

The intricate origins and diverse symptoms of Alzheimer's disease (AD) pose significant challenges for both diagnosis and treatment. Exosomes and microvesicles, which carry disease-specific cargo from a variety of central nervous system cell types, have emerged as promising reservoirs of biomarkers for AD. Research on the screening of possible biomarkers in Alzheimer's disease using proteomic profiling of EVs is systematically reviewed in this comprehensive review. We highlight key methodologies employed in EV isolation, characterization, and proteomic analysis, elucidating their advantages and limitations. Furthermore, we summarize the evolving landscape of EV-associated biomarkers implicated in AD pathogenesis, including proteins involved in amyloid-beta metabolism, tau phosphorylation, neuroinflammation, synaptic dysfunction, and neuronal injury. The literature review highlights the necessity for robust validation strategies and standardized protocols to effectively transition EV-based biomarkers into clinical use. In the concluding section, this review delves into potential future avenues and technological advancements pivotal in crafting EV-derived biomarkers applicable to AD diagnostics and prognostics. This review contributes to our comprehension of AD pathology and the advancement of precision medicine in neurodegenerative diseases, hinting at a promising era in AD precision medicine.

摘要

阿尔茨海默病(AD)的复杂起源和多种症状给诊断和治疗带来了重大挑战。外泌体和微泡携带着来自各种中枢神经系统细胞类型的疾病特异性货物,已成为 AD 生物标志物的有希望的储库。本综述系统地综述了使用 EVs 的蛋白质组谱分析筛选 AD 中可能的生物标志物的研究。我们强调了 EV 分离、表征和蛋白质组分析中使用的关键方法,阐明了它们的优点和局限性。此外,我们总结了与 AD 发病机制相关的 EV 相关生物标志物的不断发展的格局,包括参与淀粉样蛋白-β代谢、tau 磷酸化、神经炎症、突触功能障碍和神经元损伤的蛋白质。文献综述强调了需要稳健的验证策略和标准化协议,以有效地将基于 EV 的生物标志物转化为临床应用。在结论部分,本综述深入探讨了潜在的未来途径和关键技术进步,这些进步对于制作适用于 AD 诊断和预后的 EV 衍生生物标志物至关重要。本综述有助于我们理解 AD 的病理学,并推动神经退行性疾病的精准医学,预示着 AD 精准医学的一个充满希望的时代。

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