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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Activity-dependent recruitment of extrasynaptic NMDA receptor activation at an AMPA receptor-only synapse.
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Activity-dependent recruitment of extrasynaptic NMDA receptor activation at an AMPA receptor-only synapse.

机译:仅AMPA受体突触的突触外NMDA受体激活的活性依赖募集。

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摘要

We have identified an excitatory synapse in cerebellar molecular layer interneurons at which the level of presynaptic activity determines the receptor type involved in the postsynaptic response. When small numbers of parallel fibers are activated, EPSCs are mediated solely by AMPA receptors (AMPARs), despite our finding that NMDA receptors (NMDARs) are present in the dendrites of these cells. The EPSC kinetics are fast (tau decay = 0.82 +/- 0.05 msec at room temperature), consistent with the role these interneurons are thought to play in precisely timed inhibitory control of Purkinje cells. NMDARs are activated only when glutamate release is increased either by facilitation with brief high-frequency trains or by recruiting more presynaptic fibers with higher stimulus intensities. Under these conditions, EPSCs consist of a fast-rising AMPAR-mediated current followed by a slow component mediated by both NMDARs and AMPARs. Inhibitors of glutamate transport increase the amplitude and prolong the time course of the compound EPSCs. In contrast, the properties of fast AMPAR EPSCs resulting from the activation of few inputs remain unchanged when glutamate uptake is blocked. Our results suggest that, at these synapses, the postsynaptic density contains AMPARs alone. It is only when transmitter release is high enough for glutamate to diffuse to the extrasynaptic space and to reach concentrations sufficient to activate extrasynaptic receptors that NMDARs are involved in the postsynaptic response. We suggest that such a spatial separation of receptor types may provide a mechanism for rapid changes in EPSC properties, depending on the amount of synaptic activity.
机译:我们已经确定了小脑分子层interneurons中的兴奋性突触,在突触前活动的水平决定了参与突触后反应的受体类型。当激活少量平行纤维时,尽管我们发现这些细胞的树突中存在NMDA受体(NMDAR),但EPSC仅由AMPA受体(AMPAR)介导。 EPSC动力学快速(室温下tau衰减= 0.82 +/- 0.05毫秒),与这些中间神经元在精确定时的Purkinje细胞抑制控制中发挥的作用一致。仅当通过短暂的高频训练或通过募集更多具有较高刺激强度的突触前纤维来增加谷氨酸盐释放时,才激活NMDAR。在这些条件下,EPSC由快速上升的AMPAR介导的电流和随后由NMDAR和AMPAR介导的缓慢的分量组成。谷氨酸转运抑制剂增加了复合EPSC的幅度并延长了时间。相反,当谷氨酸吸收被阻止时,由少量输入激活引起的快速AMPAR EPSC的特性保持不变。我们的结果表明,在这些突触中,突触后密度仅包含AMPAR。只有当递质释放足够高以使谷氨酸扩散到突触外空间并达到足以激活突触外受体的浓度时,NMDAR才参与突触后反应。我们建议这种类型的受体类型的空间分隔可能提供一种机制,根据突触活性的数量快速改变EPSC属性。

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