Department of Pharmacology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Department of Pharmacology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Cell Rep. 2019 Mar 19;26(12):3284-3297.e3. doi: 10.1016/j.celrep.2019.02.070.
Inhibitory synapses mediate the majority of synaptic inhibition in the brain, thereby controlling neuronal excitability, firing, and plasticity. Although essential for neuronal function, the central question of how these synapses are organized at the subsynaptic level remains unanswered. Here, we use three-dimensional (3D) super-resolution microscopy to image key components of the inhibitory postsynaptic domain and presynaptic terminal, revealing that inhibitory synapses are organized into nanoscale subsynaptic domains (SSDs) of the gephyrin scaffold, GABARs and the active-zone protein Rab3-interacting molecule (RIM). Gephyrin SSDs cluster GABAR SSDs, demonstrating nanoscale architectural interdependence between scaffold and receptor. GABAR SSDs strongly associate with active-zone RIM SSDs, indicating an important role for GABAR nanoscale organization near sites of GABA release. Finally, we find that in response to elevated activity, synapse growth is mediated by an increase in the number of postsynaptic SSDs, suggesting a modular mechanism for increasing inhibitory synaptic strength.
抑制性突触在大脑中介导了大多数的突触抑制,从而控制神经元的兴奋性、发放和可塑性。尽管这些突触对于神经元功能至关重要,但它们在亚突触水平上是如何组织的这一核心问题仍未得到解答。在这里,我们使用三维(3D)超分辨率显微镜来成像抑制性突触后域和突触前末端的关键成分,揭示了抑制性突触被组织成网格蛋白支架、GABAR 和活性区蛋白 Rab3 相互作用分子(RIM)的纳米级亚突触域(SSD)。网格蛋白 SSD 簇集 GABAR SSD,表明支架和受体之间存在纳米级结构的相互依赖性。GABAR SSD 与活性区 RIM SSD 强烈关联,表明 GABAR 在 GABA 释放位点附近的纳米级组织具有重要作用。最后,我们发现,在活性增加时,突触的生长是通过增加突触后 SSD 的数量来介导的,这表明增加抑制性突触强度的一种模块化机制。