Washbourne Philip, Liu Xiao-Bo, Jones Edward G, McAllister A Kimberley
Center for Neuroscience, University of California Davis, Davis, California 95616, USA.
J Neurosci. 2004 Sep 22;24(38):8253-64. doi: 10.1523/JNEUROSCI.2555-04.2004.
The trafficking of glutamate receptors in neurons is of the utmost importance for synapse formation and synaptic plasticity. Recently, we demonstrated that both NMDA and AMPA receptors reside in mobile transport packets that are recruited rapidly and independently to nascent synapses. Here, we show that a large proportion of the glutamate receptor clusters in young cortical neurons are present on the surface of dendrites before synapses are formed and these surface-exposed transport packets are mobile. Exocytosis of glutamate receptors to the dendritic surface occurs via a SNARE [soluble n-ethylmaleimide-sensitive factor attachment protein (SNAP) receptor]-dependent SNAP-23-mediated mechanism. Endocytosis occurs rapidly after surface exposure; >50% of surface-labeled NMDA receptors (NMDARs) are endocytosed within 5 min. NMDARs are transported along microtubules on large tubulovesicular organelles, as indicated by immunoelectron microscopy, and are associated with EEA1 (early endosomal antigen 1) and SAP102 (synapse-associated protein 102), as indicated by immunocytochemistry. Most surprisingly, a large proportion of these transport packets cycle through the dendritic plasma membrane before synapse formation. These results suggest a novel model in which NMDARs cycle with the plasma membrane during pauses of movement along microtubules while trafficking.
神经元中谷氨酸受体的运输对于突触形成和突触可塑性至关重要。最近,我们证明N-甲基-D-天冬氨酸(NMDA)受体和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体都存在于可移动的运输小泡中,这些小泡能迅速且独立地被募集到新生突触处。在此,我们表明,在突触形成之前,年轻皮质神经元中很大一部分谷氨酸受体簇存在于树突表面,并且这些暴露于表面的运输小泡是可移动的。谷氨酸受体向树突表面的胞吐作用通过一种依赖可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)的、由SNAP-23介导的机制发生。表面暴露后内吞作用迅速发生;5分钟内超过50%的表面标记NMDA受体(NMDARs)被内吞。免疫电子显微镜显示,NMDARs沿着微管在大型管状囊泡细胞器上运输,免疫细胞化学显示,它们与早期内体抗原1(EEA1)和突触相关蛋白102(SAP102)相关。最令人惊讶的是,在突触形成之前,这些运输小泡中的很大一部分在树突质膜中循环。这些结果提示了一种新模型,即在运输过程中,NMDARs在沿着微管移动的暂停期间与质膜循环。