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Aβ∗56是一种稳定的寡聚体,会损害小鼠的记忆功能。

Aβ∗56 is a stable oligomer that impairs memory function in mice.

作者信息

Liu Peng, Lapcinski Ian P, Hlynialuk Chris J W, Steuer Elizabeth L, Loude Thomas J, Shapiro Samantha L, Kemper Lisa J, Ashe Karen H

机构信息

N. Bud Grossman Center for Memory Research and Care, Minneapolis, MN 55455, USA.

Department of Neurology, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

iScience. 2024 Feb 15;27(3):109239. doi: 10.1016/j.isci.2024.109239. eCollection 2024 Mar 15.

Abstract

Amyloid-β (Aβ) oligomers consist of fibrillar and non-fibrillar soluble assemblies of the Aβ peptide. Aβ∗56 is a non-fibrillar Aβ assembly that is linked to memory deficits. Previous studies did not decipher specific forms of Aβ present in Aβ∗56. Here, we confirmed the memory-impairing characteristics of Aβ∗56 and extended its biochemical characterization. We used anti-Aβ(1-x), anti-Aβ(x-40), anti-Aβ(x-42), and A11 anti-oligomer antibodies in conjunction with western blotting, immunoaffinity purification, and size-exclusion chromatography to probe aqueous brain extracts from Tg2576, 5xFAD, and APP/TTA mice. In Tg2576, Aβ∗56 is a ∼56-kDa, SDS-stable, A11-reactive, non-plaque-dependent, water-soluble, brain-derived oligomer containing canonical Aβ(1-40). In 5xFAD, Aβ∗56 is composed of Aβ(1-42), whereas in APP/TTA, it contains both Aβ(1-40) and Aβ(1-42). When injected into the hippocampus of wild-type mice, Aβ∗56 derived from Tg2576 mice impairs memory. The unusual stability of this oligomer renders it an attractive candidate for studying relationships between molecular structure and effects on brain function.

摘要

淀粉样β蛋白(Aβ)寡聚体由Aβ肽的纤维状和非纤维状可溶性聚集体组成。Aβ∗56是一种与记忆缺陷相关的非纤维状Aβ聚集体。以往的研究并未解读Aβ∗56中存在的Aβ的特定形式。在此,我们证实了Aβ∗56损害记忆的特性,并扩展了其生化特征描述。我们将抗Aβ(1-x)、抗Aβ(x-40)、抗Aβ(x-42)和A11抗寡聚体抗体与蛋白质免疫印迹、免疫亲和纯化和尺寸排阻色谱法结合使用,以检测来自Tg2576、5xFAD和APP/TTA小鼠的脑水提取物。在Tg2576小鼠中,Aβ∗56是一种约56 kDa、SDS稳定、A11反应性、不依赖斑块、水溶性、源自脑内的寡聚体,包含典型的Aβ(1-40)。在5xFAD小鼠中,Aβ∗56由Aβ(1-42)组成,而在APP/TTA小鼠中,它同时包含Aβ(1-40)和Aβ(1-42)。当将源自Tg25�6小鼠的Aβ∗56注射到野生型小鼠的海马体中时,会损害记忆。这种寡聚体不同寻常的稳定性使其成为研究分子结构与对脑功能影响之间关系的一个有吸引力的候选对象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcee/10905009/65f03a322253/fx1.jpg

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