Choquet Daniel, Opazo Patricio, Zhang Hongyu
Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297, 33000, Bordeaux, France.
Univ. Bordeaux, CNRS, INSERM, Bordeaux Imaging Center, BIC, UAR 3420, US 4, 33000, Bordeaux, France.
Transl Neurodegener. 2025 Feb 11;14(1):8. doi: 10.1186/s40035-025-00470-z.
Over the past two decades, there has been a growing recognition of the physiological importance and pathological implications surrounding the surface diffusion of AMPA receptors (AMPARs) and their diffusional trapping at synapses. AMPAR surface diffusion entails the thermally powered random Brownian lateral movement of these receptors within the plasma membrane, facilitating dynamic exchanges between synaptic and extrasynaptic compartments. This process also enables the activity-dependent diffusional trapping and accumulation of AMPARs at synapses through transient binding to synaptic anchoring slots. Recent research highlights the critical role of synaptic recruitment of AMPARs via diffusional trapping in fundamental neural processes such as the development of the early phases of long-term potentiation (LTP), contextual fear memory, memory consolidation, and sensory input-induced cortical remapping. Furthermore, studies underscore that regulation of AMPAR diffusional trapping is altered across various neurological disease models, including Huntington's disease (HD), Alzheimer's disease (AD), and stress-related disorders like depression. Notably, pharmacological interventions aimed at correcting deficits in AMPAR diffusional trapping have demonstrated efficacy in restoring synapse numbers, LTP, and memory functions in these diverse disease models, despite their distinct pathogenic mechanisms. This review provides current insights into the molecular mechanisms underlying the dysregulation of AMPAR diffusional trapping, emphasizing its role as a converging point for multiple pathological signaling pathways. We propose that targeting AMPAR diffusional trapping represents a promising early therapeutic strategy to mitigate synaptic plasticity and memory deficits in a spectrum of brain disorders, encompassing but not limited to HD, AD, and stress-related conditions. This approach underscores an integrated therapeutic target amidst the complexity of these neurodegenerative and neuropsychiatric diseases.
在过去二十年中,人们越来越认识到α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)的表面扩散及其在突触处的扩散捕获所具有的生理重要性和病理意义。AMPAR表面扩散是指这些受体在质膜内进行由热驱动的随机布朗横向运动,促进突触和突触外区室之间的动态交换。这一过程还通过与突触锚定位点的短暂结合,使AMPARs能够在活动依赖的情况下在突触处进行扩散捕获和积累。最近的研究突出了通过扩散捕获进行的AMPARs突触募集在诸如长时程增强(LTP)早期阶段的发育、情境恐惧记忆、记忆巩固以及感觉输入诱导的皮质重映射等基本神经过程中的关键作用。此外,研究强调,在包括亨廷顿病(HD)、阿尔茨海默病(AD)以及抑郁症等与应激相关的疾病模型中,AMPAR扩散捕获的调节发生了改变。值得注意的是,旨在纠正AMPAR扩散捕获缺陷的药物干预措施,尽管这些疾病模型的致病机制各不相同,但已证明在恢复这些疾病模型中的突触数量、LTP和记忆功能方面具有疗效。本综述提供了关于AMPAR扩散捕获失调潜在分子机制的当前见解,强调了其作为多种病理信号通路汇聚点的作用。我们提出,针对AMPAR扩散捕获是一种有前景的早期治疗策略,可减轻一系列脑部疾病中的突触可塑性和记忆缺陷,包括但不限于HD、AD以及与应激相关的病症。这种方法突出了在这些神经退行性和神经精神疾病复杂性中的一个综合治疗靶点。