Gerges Nashaat Z, Backos Donald S, Rupasinghe Chamila N, Spaller Mark R, Esteban José A
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109-0632, USA.
EMBO J. 2006 Apr 19;25(8):1623-34. doi: 10.1038/sj.emboj.7601065. Epub 2006 Apr 6.
Intracellular membrane trafficking of glutamate receptors at excitatory synapses is critical for synaptic function. However, little is known about the specialized trafficking events occurring at the postsynaptic membrane. We have found that two components of the exocyst complex, Sec8 and Exo70, separately control synaptic targeting and insertion of AMPA-type glutamate receptors. Sec8 controls the directional movement of receptors towards synapses through PDZ-dependent interactions. In contrast, Exo70 mediates receptor insertion at the postsynaptic membrane, but it does not participate in receptor targeting. Thus, interference with Exo70 function accumulates AMPA receptors inside the spine, forming a complex physically associated, but not yet fused with the postsynaptic membrane. Electron microscopic analysis of these complexes indicates that Exo70 mediates AMPA receptor insertion directly within the postsynaptic density, rather than at extrasynaptic membranes. Therefore, we propose a molecular and anatomical model that dissects AMPA receptor sorting and synaptic delivery within the spine, and uncovers new functions of the exocyst at the postsynaptic membrane.
兴奋性突触处谷氨酸受体的细胞内膜运输对突触功能至关重要。然而,对于突触后膜上发生的特殊运输事件却知之甚少。我们发现,外排体复合物的两个组分Sec8和Exo70分别控制AMPA型谷氨酸受体的突触靶向和插入。Sec8通过依赖PDZ的相互作用控制受体向突触的定向移动。相比之下,Exo70介导受体在突触后膜的插入,但不参与受体靶向。因此,干扰Exo70功能会使AMPA受体在棘突内积累,形成一种与突触后膜物理相关但尚未融合的复合物。对这些复合物的电子显微镜分析表明,Exo70直接介导AMPA受体在突触后致密部内插入,而非在突触外膜插入。因此,我们提出了一个分子和解剖学模型,该模型剖析了棘突内AMPA受体的分选和突触传递,并揭示了外排体在突触后膜的新功能。