基于患者iPSC的模型和人类死后海马组织的蛋白质组学分析揭示了阿尔茨海默病发病机制的早期细胞功能障碍和进展。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Yuriy Pomeshchik, Erika Velasquez, Jeovanis Gil, Oxana Klementieva, Ritha Gidlöf, Marie Sydoff, Silvia Bagnoli, Benedetta Nacmias, Sandro Sorbi, Gunilla Westergren-Thorsson, Gunnar K Gouras, Melinda Rezeli, Laurent Roybon
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引用次数: 0

摘要

海马体是阿尔茨海默病(AD)的主要影响区域。由于AD死后的脑组织在症状阶段之前是不可用的,我们缺乏对早期细胞致病机制的了解。为了解决这个问题,我们通过比较基于患者的模型系统,包括移植到小鼠脑海马中的iPSC衍生的脑细胞,来研究AD发病机制的细胞起源和进展。移植物的蛋白质组学分析能够识别AD患者脑细胞中与Aβ-42和β-片结构水平增加相关的通路和网络功能障碍。有趣的是,AD移植物周围的宿主细胞也表现出细胞生物学途径的改变。此外,基于人iPSC的模型和人死后海马组织的蛋白质组学分析显示了连贯的纵向细胞变化,表明早期至晚期AD细胞发病机制。我们的数据展示了研究AD发病机制的细胞自主起源和进展的基于患者的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction and progression of Alzheimer's disease pathogenesis.

Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction and progression of Alzheimer's disease pathogenesis.

Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction and progression of Alzheimer's disease pathogenesis.

Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction and progression of Alzheimer's disease pathogenesis.

The hippocampus is a primary region affected in Alzheimer's disease (AD). Because AD postmortem brain tissue is not available prior to symptomatic stage, we lack understanding of early cellular pathogenic mechanisms. To address this issue, we examined the cellular origin and progression of AD pathogenesis by comparing patient-based model systems including iPSC-derived brain cells transplanted into the mouse brain hippocampus. Proteomic analysis of the graft enabled the identification of pathways and network dysfunction in AD patient brain cells, associated with increased levels of Aβ-42 and β-sheet structures. Interestingly, the host cells surrounding the AD graft also presented alterations in cellular biological pathways. Furthermore, proteomic analysis across human iPSC-based models and human post-mortem hippocampal tissue projected coherent longitudinal cellular changes indicative of early to end stage AD cellular pathogenesis. Our data showcase patient-based models to study the cell autonomous origin and progression of AD pathogenesis.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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