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通过冷冻电镜断层扫描对天然突触前细胞外基质进行定量分析。

Quantitative analysis of the native presynaptic cytomatrix by cryoelectron tomography.

机构信息

Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, D-82152 Martinsried, Germany.

出版信息

J Cell Biol. 2010 Jan 11;188(1):145-56. doi: 10.1083/jcb.200908082.

Abstract

The presynaptic terminal contains a complex network of filaments whose precise organization and functions are not yet understood. The cryoelectron tomography experiments reported in this study indicate that these structures play a prominent role in synaptic vesicle release. Docked synaptic vesicles did not make membrane to membrane contact with the active zone but were instead linked to it by tethers of different length. Our observations are consistent with an exocytosis model in which vesicles are first anchored by long (>5 nm) tethers that give way to multiple short tethers once vesicles enter the readily releasable pool. The formation of short tethers was inhibited by tetanus toxin, indicating that it depends on soluble N-ethyl-maleimide sensitive fusion protein attachment protein receptor complex assembly. Vesicles were extensively interlinked via a set of connectors that underwent profound rearrangements upon synaptic stimulation and okadaic acid treatment, suggesting a role of these connectors in synaptic vesicle mobilization and neurotransmitter release.

摘要

突触前末梢包含一个复杂的纤维网络,其确切的组织和功能尚不清楚。本研究报告的低温电子断层扫描实验表明,这些结构在突触囊泡释放中起着重要作用。停靠的突触囊泡与活性区没有膜对膜的接触,而是通过不同长度的连接物与之相连。我们的观察结果与一个胞吐模型一致,即囊泡首先通过长 (>5nm)的连接物锚定,一旦囊泡进入易释放池,就会形成多个短连接物。短连接物的形成被破伤风毒素抑制,表明它依赖于可溶性 N-乙基-马来酰亚胺敏感融合蛋白附着蛋白受体复合物的组装。囊泡通过一组连接器广泛交联,这些连接器在突触刺激和 okadaic 酸处理时会发生深刻的重排,表明这些连接器在突触囊泡动员和神经递质释放中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82da/2812849/87d8667b6476/JCB_200908082_GS_Fig1.jpg

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