McGovern Institute for Brain Research and Department of Brain and Cognitive Science, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Dev Neurobiol. 2010 Sep 15;70(11):737-50. doi: 10.1002/dneu.20807.
At the onset of a period of intense synaptic refinement initiated by synchronized eye opening (EO), rapid changes in postsynaptic NMDA receptor and AMPA receptor currents (NMDARcs and AMPARcs) occur within the superficial visual layers of the rodent superior colliculus (sSC; Lu and Constantine-Paton [2004]: Neuron 43:237-249). Subsequently, evoked non-NMDARc amplitudes increase, but by 2 weeks after EO (AEO) they decrease significantly. Here, using whole-cell patch-clamp recording, we demonstrate that small, slowly desensitizing excitatory kainate receptor currents (KARcs) are responsible for the rise and subsequent fall in non-NMDARcs. The increase in KAR transmission parallels inhibitory GABA(A) responses that plateau at 7 days AEO. By 2 weeks AEO, KARcs are gone. AMPARcs remain unchanged during the appearance and disappearance of the KARcs, despite increases in sSC neuropil activity and continued refinement of inputs to individual sSC neurons. We suggest that in the interval of heightened activity, before SC inhibition matures, many AMPARcs desensitize and are relatively ineffective at relieving the Mg(2+) block on NMDARs. This transient appearance of slowly desensitizing, long-duration KARcs may provide increased membrane depolarization necessary for NMDAR function and continuation of synaptic refinement.
在由同步睁眼 (EO) 引发的强烈突触精炼期开始时,在啮齿动物上丘的浅层视觉层中,会发生快速的突触后 NMDA 受体和 AMPA 受体电流 (NMDARcs 和 AMPARcs) 变化 (Lu 和 Constantine-Paton [2004]: Neuron 43:237-249)。随后,诱发的非 NMDA 受体电流幅度增加,但在 EO 后 2 周 (AEO) 时显著下降。在这里,我们使用全细胞膜片钳记录技术证明,小而缓慢脱敏的兴奋性海人酸受体电流 (KARcs) 是导致非 NMDA 受体电流上升和随后下降的原因。KAR 传递的增加与抑制性 GABA(A) 反应平行,后者在 7 天 AEO 时达到平台期。到 2 周 AEO 时,KARcs 消失。尽管 sSC 神经突活动增加并且输入到单个 sSC 神经元的输入继续细化,但在 KARcs 出现和消失期间,AMPA 受体电流保持不变。我们认为,在 SC 抑制成熟之前的高活动期内,许多 AMPARcs 脱敏,并且在缓解 NMDA 受体上的 Mg(2+) 阻断方面相对无效。这种缓慢脱敏、长时程 KARcs 的短暂出现可能提供了 NMDA 受体功能和突触精炼持续所需的增加的膜去极化。