阿尔茨海默病患者大脑中淀粉样蛋白寡聚体的可视化研究

IF 1.6 4区 生物学 Q4 CELL BIOLOGY
Ikuo Tooyama, Tomoko Kato, Hiroyasu Taguchi, Yusuke Kageyama, Kazuhiro Irie, Yukie Hirahara, Daijiro Yanagisawa
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引用次数: 0

摘要

在阿尔茨海默病(AD)的发病机制中,高神经毒性的淀粉样蛋白-β(Aβ)低聚物出现得很早,因此被认为与阿尔茨海默病的发病有很大关系。然而,由于 Aβ 寡聚体有多种形态(如低分子量和高分子量寡聚体,包括原纤维),而且容易迅速改变形态和聚集,因此在人体组织中进行 Aβ 寡聚体可视化具有挑战性。在本综述中,我们介绍了组织中 Aβ 寡聚体的两种可视化方法:免疫组化法(使用针对有毒 Aβ 寡聚体构象的单克隆抗体 TxCo1)和成像质谱法(使用能特异性结合 Aβ 寡聚体的小化学物 Shiga-Y51)。TxCo1免疫组化显示了AD患者死后大脑中Aβ寡聚体的分布。使用Shiga-Y51,成像质谱法揭示了AD转基因小鼠大脑中Aβ寡聚体的分布。这两种方法可能有助于阐明AD的病理机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visualization of Amyloid Oligomers in the Brain of Patients with Alzheimer’s Disease

In the pathogenesis of Alzheimer’s disease (AD), highly neurotoxic amyloid-β (Aβ) oligomers appear early, they are thus considered to be deeply involved in the onset of Alzheimer’s disease. However, Aβ oligomer visualization is challenging in human tissues due to their multiple forms (e.g., low- and high-molecular-weight oligomers, including protofibrils) as well as their tendency to rapidly change forms and aggregate. In this review, we present two visualization approaches for Aβ oligomers in tissues: an immunohistochemical (using the monoclonal antibody TxCo1 against toxic Aβ oligomer conformers) and imaging mass spectrometry using the small chemical Shiga-Y51 that specifically binds Aβ oligomers. TxCo1 immunohistochemistry revealed Aβ oligomer distributions in postmortem human brains with AD. Using Shiga-Y51, imaging mass spectrometry revealed Aβ oligomer distributions in the brain of a transgenic mouse model for AD. These two methods would potentially contribute to elucidating the pathological mechanisms underlying AD.

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来源期刊
Acta Histochemica Et Cytochemica
Acta Histochemica Et Cytochemica 生物-细胞生物学
CiteScore
3.50
自引率
8.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: Acta Histochemica et Cytochemica is the official online journal of the Japan Society of Histochemistry and Cytochemistry. It is intended primarily for rapid publication of concise, original articles in the fields of histochemistry and cytochemistry. Manuscripts oriented towards methodological subjects that contain significant technical advances in these fields are also welcome. Manuscripts in English are accepted from investigators in any country, whether or not they are members of the Japan Society of Histochemistry and Cytochemistry. Manuscripts should be original work that has not been previously published and is not being considered for publication elsewhere, with the exception of abstracts. Manuscripts with essentially the same content as a paper that has been published or accepted, or is under consideration for publication, will not be considered. All submitted papers will be peer-reviewed by at least two referees selected by an appropriate Associate Editor. Acceptance is based on scientific significance, originality, and clarity. When required, a revised manuscript should be submitted within 3 months, otherwise it will be considered to be a new submission. The Editor-in-Chief will make all final decisions regarding acceptance.
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