首页> 美国卫生研究院文献>The Journal of Neuroscience >Super-Resolution Imaging Reveals That AMPA Receptors Inside Synapses Are Dynamically Organized in Nanodomains Regulated by PSD95
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Super-Resolution Imaging Reveals That AMPA Receptors Inside Synapses Are Dynamically Organized in Nanodomains Regulated by PSD95

机译:超分辨率成像显示突触内部的AMPA受体在受PSD95调控的纳米域中动态组织。

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摘要

The spatiotemporal organization of neurotransmitter receptors in postsynaptic membranes is a fundamental determinant of synaptic transmission and information processing by the brain. Using four independent super-resolution light imaging methods and EM of genetically tagged and endogenous receptors, we show that, in rat hippocampal neurons, AMPARs are often highly concentrated inside synapses into a few clusters of ∼70 nm that contain ∼20 receptors. AMPARs are stabilized reversibly in these nanodomains and diffuse freely outside them. Nanodomains are dynamic in their shape and position within synapses and can form or disappear within minutes, although they are mostly stable for up to 1 h. AMPAR nanodomains are often, but not systematically, colocalized with clusters of the scaffold protein PSD95, which are generally of larger size than AMPAR nanoclusters. PSD95 expression level regulates AMPAR nanodomain size and compactness in parallel to miniature EPSC amplitude. Monte Carlo simulations further indicate the impact of AMPAR concentration in clusters on the efficacy of synaptic transmission. The observation that AMPARs are highly concentrated in nanodomains, instead of diffusively distributed in the PSD as generally thought, has important consequences on our understanding of excitatory neurotransmission. Furthermore, our results indicate that glutamatergic synaptic transmission is controlled by the nanometer-scale regulation of the size of these highly concentrated nanodomains.
机译:突触后膜中神经递质受体的时空组织是大脑突触传递和信息处理的基本决定因素。我们使用四种独立的超高分辨率光成像方法以及遗传标记和内源性受体的EM,我们发现,在大鼠海马神经元中,AMPAR通常高度集中在突触内部,形成约70 nm的几个簇,其中包含约20个受体。 AMPAR可逆地稳定在这些纳米域中,并在其外部自由扩散。纳米域在突触中的形状和位置是动态的,并且可以在数分钟内形成或消失,尽管它们最多可稳定长达1小时。 AMPAR纳米域通常但不是系统地与支架蛋白PSD95簇共定位,该簇蛋白通常比AMPAR纳米簇大。 PSD95的表达水平调节AMPAR纳米域的大小和紧密度,以平行于微型EPSC振幅。蒙特卡洛模拟进一步表明,簇中AMPAR浓度对突触传递功效的影响。 AMPARs高度集中在纳米域中,而不是像通常认为的那样扩散分布在PSD中,这一发现对我们对兴奋性神经传递的理解具有重要意义。此外,我们的结果表明,谷氨酸能突触传递受这些高度浓缩的纳米域的大小的纳米级调节控制。

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