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淀粉样β肽序列第 22 位的家族性阿尔茨海默病突变在体外系统中不同程度地影响突触丢失、tau 磷酸化和神经元细胞死亡。

Familial Alzheimer's disease mutations at position 22 of the amyloid β-peptide sequence differentially affect synaptic loss, tau phosphorylation and neuronal cell death in an ex vivo system.

机构信息

Institute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.

Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland.

出版信息

PLoS One. 2020 Sep 23;15(9):e0239584. doi: 10.1371/journal.pone.0239584. eCollection 2020.

Abstract

Familial forms of Alzheimer's disease (AD) are caused by mutations in the presenilin genes or in the gene encoding for the amyloid precursor protein (APP). Proteolytic cleavage of APP generates the β-amyloid peptide (Aβ), which aggregates into amyloid plaques, one of the major hallmarks of AD. APP mutations within the Aβ sequence, so-called intra-Aβ mutations, cluster around position E693 of APP, which corresponds to position E22 in the Aβ sequence. One of these mutations is the Osaka mutation, E693Δ, which has unique aggregation properties with patients showing unusually low brain amyloid levels on amyloid PET scans. Despite intense research on the pathomechanisms of different intra-Aβ mutants, our knowledge is limited due to controversial findings in various studies. Here, we investigated in an ex vivo experimental system the neuro- and synaptotoxic properties of two intra-Aβ mutants with different intrinsic aggregation propensities, the Osaka mutation E22Δ and the Arctic mutation E22G, and compared them to wild-type (wt) Aβ. Experiments in hippocampal slice cultures from transgenic mice were complemented by treating wild-type slices with recombinantly produced Aβ40 or Aβ42 containing the respective intra-Aβ mutations. Our analyses revealed that wt Aβ and E22G Aβ, both recombinant and transgenic, caused a loss of dendritic spines along with an increase in tau phosphorylation and tau-dependent neurodegeneration. In all experiments, the 42-residue variants of wt and E22G Aβ showed stronger effects than the respective Aβ40 isoforms. In contrast, E22Δ Aβ neither reduced dendritic spine density nor resulted in increased tau phosphorylation or neuronal cell death in our ex vivo system. Our findings suggest that the previously reported major differences in the aggregation kinetics between E22G and E22Δ Aβ are likely reflected in different disease pathomechanisms.

摘要

阿尔茨海默病(AD)的家族形式是由早老素基因或淀粉样前体蛋白(APP)编码基因突变引起的。APP 的蛋白水解切割生成 β-淀粉样肽(Aβ),其聚集形成淀粉样斑块,这是 AD 的主要标志之一。APP 中 Aβ 序列内的突变,即所谓的 Aβ 内突变,聚集在 APP 的 E693 位置周围,该位置对应于 Aβ 序列中的 E22 位置。这些突变之一是大阪突变,E693Δ,具有独特的聚集特性,患者在淀粉样 PET 扫描上表现出异常低的脑淀粉样蛋白水平。尽管对不同 Aβ 内突变体的病理机制进行了深入研究,但由于各种研究中的争议发现,我们的知识仍然有限。在这里,我们在离体实验系统中研究了两种具有不同内在聚集倾向的 Aβ 内突变体的神经毒性和突触毒性特性,即大阪突变 E22Δ 和北极突变 E22G,并将其与野生型(wt)Aβ进行了比较。从转基因小鼠海马切片培养物进行的实验补充了用重组产生的含有各自 Aβ 内突变的 Aβ40 或 Aβ42 处理野生型切片的实验。我们的分析表明,wt Aβ 和 E22G Aβ,无论是重组的还是转基因的,都会导致树突棘丢失,同时伴有 tau 磷酸化和 tau 依赖性神经退行性变增加。在所有实验中,wt 和 E22G Aβ 的 42 个残基变体比各自的 Aβ40 同工型表现出更强的作用。相比之下,E22Δ Aβ 在我们的离体系统中既不会降低树突棘密度,也不会导致 tau 磷酸化或神经元细胞死亡增加。我们的研究结果表明,先前报道的 E22G 和 E22Δ Aβ 之间在聚集动力学方面的主要差异可能反映了不同的疾病病理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36ab/7510992/d75ef99faa9d/pone.0239584.g001.jpg

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