Laboratory of cell Physiology of the synapse, CNRS, UMR 5091, Bordeaux, France.
Eur J Neurosci. 2010 Jul;32(2):250-60. doi: 10.1111/j.1460-9568.2010.07350.x. Epub 2010 Jul 14.
AMPA-type glutamate receptors (AMPARs), as well as most other transmembrane proteins, are not stable in the postsynaptic density as was previously thought, but undergo constant trafficking in and out of synapses by a combination of endo/exocytosis and lateral diffusion. The respective contributions of membrane recycling events and surface trafficking to setting AMPAR numbers at synapses have been the subject of intense debate. Although this discussion is not yet settled, it is safe to state that both categories of processes participate in receptor exchange at synapses at rest and during various forms of plasticity. More unexpectedly, AMPARs can diffuse at such high rates within the postsynaptic density itself that their surface trafficking could participate not only in setting receptor numbers at individual synapses but also in tuning synaptic transmission during short-term plasticity. I here review recent results that characterize the activity-dependent properties of AMPAR surface trafficking and their possible links to fast synaptic transmission.
AMPA 型谷氨酸受体 (AMPARs) 以及大多数其他跨膜蛋白,并不像之前认为的那样在突触后密度中稳定存在,而是通过内吞/胞吐作用和侧向扩散的组合,不断在突触内外运输。膜回收事件和表面运输对确定突触中 AMPAR 数量的各自贡献一直是激烈争论的主题。尽管这一讨论尚未解决,但可以肯定的是,这两类过程都参与了静息和各种形式可塑性时突触处的受体交换。更出人意料的是,AMPA 受体在突触后密度内的扩散速度如此之高,以至于它们的表面运输不仅可以参与确定单个突触的受体数量,还可以在短期可塑性过程中调节突触传递。我在这里回顾了最近的一些结果,这些结果描述了 AMPAR 表面运输的活动依赖性特性及其与快速突触传递的可能联系。