Perestenko Pavel V, Henley Jeremy M
Medical Research Council Centre for Synaptic Plasticity, Department of Anatomy, University of Bristol, School of Medical Sciences, University Walk, Bristol BS8 1TD, United Kingdom.
J Biol Chem. 2003 Oct 31;278(44):43525-32. doi: 10.1074/jbc.M306206200. Epub 2003 Aug 8.
Little is known about the dynamics of the dendritic transport of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors (AMPARs) to synapses. Here, using virally expressed green fluorescent protein (GFP)-GluR1 and GFP-GluR2 and confocal photobleach techniques we show near real-time movement of these subunits in living cultured hippocampal neurons. GFP-GluR1 fluorescence was widely distributed throughout the extranuclear compartment with no evidence for discrete intracellular stores. GFP-GluR1 transport was predominantly proximal to distal at rates of 0.2-0.4 mum.s-1. GFP-GluR2 fluorescence was more punctate and localized at or close to the plasma membrane. Overall, GFP-GluR2 movement was less dynamic with distinct mobile and immobile pools. Neither activation nor inhibition of surface-expressed N-methyl-d-aspartate receptors or AMPARs had any significant effect on the rates of GFP-GluR1 or GFP-GluR2 dendritic transport. These results demonstrate that GluR1 is constitutively and rapidly transported throughout the neuron. GluR2, on the other hand, is less mobile, with a majority retained in relatively immobile membrane-associated clusters, with approximately 40% showing synaptic co-localization. Furthermore, the transport of both subunits is activity-independent, suggesting that the regulated delivery of AMPARs to the vicinity of synapses is not a mechanism that is involved in processes such as synaptic plasticity.
关于α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)向突触的树突运输动态,人们了解甚少。在此,我们利用病毒表达的绿色荧光蛋白(GFP)-GluR1和GFP-GluR2以及共聚焦光漂白技术,展示了这些亚基在活体培养海马神经元中的近实时运动。GFP-GluR1荧光广泛分布于整个核外区室,没有证据表明存在离散的细胞内储存。GFP-GluR1的运输主要是从近端到远端,速度为0.2 - 0.4μm·s⁻¹。GFP-GluR2荧光更呈点状,定位于质膜或靠近质膜处。总体而言,GFP-GluR2的运动活力较低,有明显的可移动池和不可移动池。表面表达的N-甲基-D-天冬氨酸受体或AMPARs的激活或抑制对GFP-GluR1或GFP-GluR2树突运输速率均无显著影响。这些结果表明,GluR1在整个神经元中持续且快速地运输。另一方面,GluR2的移动性较差,大多数保留在相对不可移动的膜相关簇中约40%显示出与突触共定位。此外,两个亚基的运输均不依赖于活性,这表明AMPARs向突触附近的调节性递送不是参与诸如突触可塑性等过程的机制。