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淀粉样前体蛋白在记忆形成中的作用。

Role of Amyloid Precursor Protein in Memory Formation.

作者信息

Preat Thomas, Goguel Valérie

机构信息

Genes and Dynamics of Memory Systems, Brain Plasticity Unit, Centre National de la Recherche Scientifique (CNRS), ESPCI Paris, PSL Research University Paris, France.

出版信息

Front Mol Neurosci. 2016 Dec 8;9:142. doi: 10.3389/fnmol.2016.00142. eCollection 2016.

DOI:10.3389/fnmol.2016.00142
PMID:28008309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5143682/
Abstract

The amyloid precursor protein (APP) is a membrane protein engaged in complex proteolytic pathways. APP and its derivatives have been shown to play a central role in Alzheimer's disease (AD), a progressive neurodegenerative disease characterized by memory decline. Despite a huge effort from the research community, the primary cause of AD remains unclear, making it crucial to better understand the physiological role of the APP pathway in brain plasticity and memory. is a model system well-suited to address this issue. Although relatively simple, the fly brain is highly organized, sustains several forms of learning and memory, and drives numerous complex behaviors. Importantly, molecules and mechanisms underlying memory processes are conserved from flies to mammals. The fly encodes a single non-essential APP homolog named APP-Like (APPL). Using inducible RNA interference strategies, it was shown that APPL knockdown in the mushroom bodies (MB)-the central integrative brain structure for olfactory memory-results in loss of memory. Several APPL derivatives, such as secreted and full-length membrane APPL, may play different roles in distinct types of memory phases. Furthermore, overexpression of amyloid peptide exacerbates the memory deficit caused by APPL knockdown, thus potentiating memory decline. Data obtained in the fly support the hypothesis that APP acts as a transmembrane receptor, and that disruption of its normal function may contribute to cognitive impairment during early AD.

摘要

淀粉样前体蛋白(APP)是一种参与复杂蛋白水解途径的膜蛋白。APP及其衍生物已被证明在阿尔茨海默病(AD)中起核心作用,AD是一种以记忆衰退为特征的进行性神经退行性疾病。尽管研究界付出了巨大努力,但AD的主要病因仍不清楚,因此更好地理解APP途径在脑可塑性和记忆中的生理作用至关重要。果蝇是一个非常适合解决这个问题的模型系统。果蝇大脑虽然相对简单,但高度有序,支持多种形式的学习和记忆,并驱动许多复杂行为。重要的是,记忆过程的分子和机制在从果蝇到哺乳动物中是保守的。果蝇编码一种名为类APP(APPL)的单一非必需APP同源物。使用诱导性RNA干扰策略表明,在蘑菇体(MB)——嗅觉记忆的中央整合脑结构中敲低APPL会导致记忆丧失。几种APPL衍生物,如分泌型和全长膜型APPL,可能在不同类型的记忆阶段发挥不同作用。此外,淀粉样肽的过表达会加剧APPL敲低引起的记忆缺陷,从而加剧记忆衰退。在果蝇中获得的数据支持以下假设:APP作为一种跨膜受体,其正常功能的破坏可能导致AD早期的认知障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1aa/5143682/52fa581f98b8/fnmol-09-00142-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1aa/5143682/52fa581f98b8/fnmol-09-00142-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1aa/5143682/52fa581f98b8/fnmol-09-00142-g0001.jpg

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本文引用的文献

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2
Amyloid-β Peptide Exacerbates the Memory Deficit Caused by Amyloid Precursor Protein Loss-of-Function in Drosophila.淀粉样β肽加剧果蝇中淀粉样前体蛋白功能丧失所导致的记忆缺陷。
PLoS One. 2015 Aug 14;10(8):e0135741. doi: 10.1371/journal.pone.0135741. eCollection 2015.
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Two independent mushroom body output circuits retrieve the six discrete components of Drosophila aversive memory.
Int J Mol Sci. 2021 Jun 29;22(13):7022. doi: 10.3390/ijms22137022.
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Amyloid Precursor Protein (APP) and GABAergic Neurotransmission.淀粉样前体蛋白(APP)与 GABA 能神经传递。
Cells. 2019 Jun 6;8(6):550. doi: 10.3390/cells8060550.
5
Suppression of the synaptic localization of a subset of proteins including APP partially ameliorates phenotypes of the Drosophila Alzheimer's disease model.抑制包括 APP 在内的一部分蛋白质的突触定位部分改善了果蝇阿尔茨海默病模型的表型。
PLoS One. 2018 Sep 18;13(9):e0204048. doi: 10.1371/journal.pone.0204048. eCollection 2018.
6
Delayed cognitive deficits can be alleviated by calcium antagonist nimodipine by downregulation of apoptosis following whole brain radiotherapy.全脑放疗后,钙拮抗剂尼莫地平可通过下调细胞凋亡来减轻延迟性认知缺陷。
Oncol Lett. 2018 Aug;16(2):2525-2532. doi: 10.3892/ol.2018.8968. Epub 2018 Jun 13.
7
Drosophila Full-Length Amyloid Precursor Protein Is Required for Visual Working Memory and Prevents Age-Related Memory Impairment.果蝇全长淀粉样前体蛋白对于视觉工作记忆是必需的,并且可以防止与年龄相关的记忆损伤。
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Cell Rep. 2015 May 26;11(8):1280-92. doi: 10.1016/j.celrep.2015.04.044. Epub 2015 May 14.
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