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淀粉样β蛋白引发的突触缺陷是由含GluA3的AMPA受体的突触清除介导的。

Amyloid-β-Driven Synaptic Deficits Are Mediated by Synaptic Removal of GluA3-Containing AMPA Receptors.

作者信息

Reinders Niels R, van der Spek Sophie J F, Klaassen Remco V, Koymans Karin J, MacGillavry Harold D, Smit August B, Kessels Helmut W

机构信息

Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam 1105 BA, The Netherlands

Swammerdam Institute of Life Sciences, Amsterdam Neuroscience, University of Amsterdam, Amsterdam 1098 XH, The Netherlands.

出版信息

J Neurosci. 2025 Feb 26;45(9):e0393242024. doi: 10.1523/JNEUROSCI.0393-24.2024.

Abstract

The detrimental effects of oligomeric amyloid-β (Aβ) on synapses are considered the leading cause for cognitive deficits in Alzheimer's disease. However, through which mechanism Aβ oligomers impair synaptic structure and function remains unknown. Here, we used electrophysiology and amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) imaging on mouse and rat neurons to demonstrate that GluA3 expression in neurons lacking GluA3 is sufficient to resensitize their synapses to the damaging effects of Aβ, indicating that GluA3-containing AMPARs at synapses are necessary and sufficient for Aβ to induce synaptic deficits. We found that Aβ oligomers trigger the endocytosis of GluA3 and promote its translocation toward endolysosomal compartments for degradation. Mechanistically, these Aβ-driven effects critically depend on the PDZ-binding motif of GluA3. A single point mutation in the GluA3 PDZ-binding motif prevented Aβ-driven effects and rendered synapses fully resistant to the effects of Aβ. Correspondingly, proteomics on synaptosome fractions from APP/PS1-transgenic mice revealed a selective reduction of GluA3 at an early age. These findings support a model where the endocytosis and lysosomal degradation of GluA3-containing AMPARs are a critical early step in the cascade of events through which Aβ accumulation causes a loss of synapses.

摘要

淀粉样前体蛋白寡聚体(Aβ)对突触的有害作用被认为是阿尔茨海默病认知缺陷的主要原因。然而,Aβ寡聚体通过何种机制损害突触结构和功能仍不清楚。在这里,我们对小鼠和大鼠神经元进行了电生理学和氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)成像,以证明缺乏GluA3的神经元中GluA3的表达足以使其突触对Aβ的破坏作用重新敏感,这表明突触处含GluA3的AMPARs对于Aβ诱导突触缺陷是必要且充分的。我们发现Aβ寡聚体触发GluA3的内吞作用,并促进其向内溶酶体区室转运以进行降解。从机制上讲,这些由Aβ驱动的效应关键取决于GluA3的PDZ结合基序。GluA3 PDZ结合基序中的单点突变可阻止Aβ驱动的效应,并使突触对Aβ的效应完全产生抗性。相应地,对APP/PS1转基因小鼠突触体组分的蛋白质组学分析显示,在早期GluA3有选择性减少。这些发现支持了一个模型,即含GluA3的AMPARs的内吞作用和溶酶体降解是Aβ积累导致突触丧失的一系列事件中的关键早期步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e21c/11867010/46fb2db74ce4/jneuro-45-e0393242024-g001.jpg

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