Siksou Léa, Rostaing Philippe, Lechaire Jean-Pierre, Boudier Thomas, Ohtsuka Toshihisa, Fejtová Anna, Kao Hung-Teh, Greengard Paul, Gundelfinger Eckart D, Triller Antoine, Marty Serge
Inserm U789, Ecole Normale Supérieure, 75005 Paris, France.
J Neurosci. 2007 Jun 27;27(26):6868-77. doi: 10.1523/JNEUROSCI.1773-07.2007.
Presynaptic terminals are specialized for mediating rapid fusion of synaptic vesicles (SVs) after calcium influx. The regulated trafficking of SVs likely results from a highly organized cytomatrix. How this cytomatrix links SVs, maintains them near the active zones (AZs) of release, and organizes docked SVs at the release sites is not fully understood. To analyze the three-dimensional (3D) architecture of the presynaptic cytomatrix, electron tomography of presynaptic terminals contacting spines was performed in the stratum radiatum of the rat hippocampal CA1 area. To preserve the cytomatrix, hippocampal slices were immobilized using high-pressure freezing, followed by cryosubstitution and embedding. SVs are surrounded by a dense network of filaments. A given vesicle is connected to approximately 1.5 neighboring ones. SVs at the periphery of this network are also linked to the plasma membrane, by longer filaments. More of these filaments are found at the AZ. At the AZ, docked SVs are grouped around presynaptic densities. Filaments with adjacent SVs emerge from these densities. Immunogold localizations revealed that synapsin is located in the presynaptic bouton, whereas Bassoon and CAST (ERC2) are at focal points next to the AZ. In synapsin triple knock-out mice, the number of SVs is reduced by 63%, but the size of the boutons is reduced by only 18%, and the mean distance of SVs to the AZ is unchanged. This 3D analysis reveals the morphological constraints exerted by the presynaptic molecular scaffold. SVs are tightly interconnected in the axonal bouton, and this network is preferentially connected to the AZ.
突触前终末专门用于在钙离子内流后介导突触小泡(SVs)的快速融合。SVs的调节性运输可能源于高度组织化的细胞基质。这种细胞基质如何连接SVs、将它们维持在释放活性区(AZs)附近以及在释放位点组织停靠的SVs,目前尚不完全清楚。为了分析突触前细胞基质的三维(3D)结构,在大鼠海马CA1区辐射层中对与棘突接触的突触前终末进行了电子断层扫描。为了保存细胞基质,使用高压冷冻固定海马切片,随后进行冷冻置换和包埋。SVs被密集的细丝网络包围。一个给定的小泡与大约1.5个相邻小泡相连。该网络周边的SVs也通过更长的细丝与质膜相连。在AZ处发现更多这样的细丝。在AZ处,停靠的SVs围绕突触前致密物聚集。与相邻SVs相连的细丝从这些致密物中伸出。免疫金定位显示,突触素位于突触前终扣中,而巴松管和CAST(ERC2)位于AZ旁边的焦点处。在突触素三联敲除小鼠中,SVs的数量减少了63%,但终扣的大小仅减少了18%,且SVs到AZ的平均距离不变。这种3D分析揭示了突触前分子支架施加的形态学限制。SVs在轴突终扣中紧密相连,并且这个网络优先与AZ相连。