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The Positive Side of the Alzheimer’s Disease Amyloid Cross-Interactions: The Case of the Aβ 1-42 Peptide with Tau TTR CysC and ApoA1

机译:阿尔茨海默氏病淀粉样蛋白交叉相互作用的积极方面:Aβ1-42肽与TauTTRCysC和ApoA1结合的情况

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摘要

Alzheimer’s disease (AD) represents a progressive amyloidogenic disorder whose advancement is widely recognized to be connected to amyloid-β peptides and Tau aggregation. However, several other processes likely contribute to the development of AD and some of them might be related to protein-protein interactions. Amyloid aggregates usually contain not only single type of amyloid protein, but also other type of proteins and this phenomenon can be rationally explained by the process of protein cross-seeding and co-assembly. Amyloid cross-interaction is ubiquitous in amyloid fibril formation and so a better knowledge of the amyloid interactome could help to further understand the mechanisms of amyloid related diseases. In this review, we discuss about the cross-interactions of amyloid-β peptides, and in particular Aβ1-42, with other amyloids, which have been presented either as integrated part of Aβ neurotoxicity process (such as Tau) or conversely with a preventive role in AD pathogenesis by directly binding to Aβ (such as transthyretin, cystatin C and apolipoprotein A1). Particularly, we will focus on all the possible therapeutic strategies aiming to rescue the Aβ toxicity by taking inspiration from these protein-protein interactions.
机译:阿尔茨海默氏病(AD)代表一种进行性淀粉样变性疾病,其进展被广泛认为与淀粉样β肽和Tau聚集有关。但是,其他几个过程可能也有助于AD的发展,其中一些可能与蛋白质-蛋白质相互作用有关。淀粉样聚集体通常不仅包含单一类型的淀粉样蛋白,而且还包含其他类型的蛋白,这种现象可以通过蛋白的交叉播种和共组装过程得到合理解释。淀粉样蛋白原纤维形成过程中普遍存在淀粉样蛋白交叉相互作用,因此对淀粉样蛋白相互作用组的更好了解有助于进一步了解淀粉样蛋白相关疾病的机制。在这篇综述中,我们讨论了淀粉样蛋白-β肽,特别是Aβ1-42与其他淀粉样蛋白的交叉相互作用,这些蛋白已被证明是Aβ神经毒性过程的整合部分(例如Tau),或者与预防性蛋白相反通过直接结合Aβ(例如运甲状腺素蛋白,胱抑素C和载脂蛋白A1)在AD发病中的作用。特别是,我们将集中于所有可能的治疗策略,旨在通过从这些蛋白质-蛋白质相互作用中汲取灵感来挽救Aβ毒性。

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