首页> 美国卫生研究院文献>The Journal of Neuroscience >The Presynaptic Dense Projection of the Caenorhabiditis elegans Cholinergic Neuromuscular Junction Localizes Synaptic Vesicles at the Active Zone through SYD-2/Liprin and UNC-10/RIM-Dependent Interactions
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The Presynaptic Dense Projection of the Caenorhabiditis elegans Cholinergic Neuromuscular Junction Localizes Synaptic Vesicles at the Active Zone through SYD-2/Liprin and UNC-10/RIM-Dependent Interactions

机译:秀丽隐杆线虫胆碱能神经肌肉连接的突触前密集投射通过SYD-2 / Liprin和UNC-10 / RIM依赖性相互作用将突触小泡定位在活性区。

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摘要

The active zone (AZ) of chemical synapses is a specialized area of the presynaptic bouton in which vesicles fuse with the plasma membrane and release neurotransmitters. Efficient signaling requires synaptic vesicles (SVs) to be recruited, primed, and retained at the AZ, in close proximity to voltage-dependent calcium channels that are activated during presynaptic depolarization. The electron-dense specializations at the AZ might provide a molecular platform for the spatial coordination of these different processes. To investigate this hypothesis, we examined high-resolution three-dimensional models of Caenorhabditis elegans cholinergic neuromuscular junctions generated by electron tomography. First, we found that SVs are interconnected within the bouton by filaments similar to those described in vertebrates. Second, we resolved the three-dimensional structure of the dense projection centered in the AZ. The dense projection is a more complex structure than previously anticipated, with filaments radiating from a core structure that directly contact SVs in the interior of the bouton as well as SVs docked at the plasma membrane. Third, we investigated the functional correlate of these contacts by analyzing mutants disrupting two key AZ proteins: UNC-10/RIM and SYD-2/liprin. In both mutants, the number of contacts between SVs and the dense projection was significantly reduced. Similar to unc-10 mutants, the dependence of SV fusion on extracellular calcium concentration was exacerbated in syd-2 mutants when compared with the wild type. Hence, we propose that the dense projection ensures proper coupling of primed vesicles with calcium signaling by retaining them at the AZ via UNC-10/RIM and SYD-2/liprin-dependent mechanisms.
机译:化学突触的活动区(AZ)是突触前钮扣的特殊区域,囊泡与质膜融合并释放神经递质。有效的信号传导需要突触小泡(SVs)在突触前去极化过程中被激活的电压依赖性钙离子通道附近被募集,引发和保留在AZ。 AZ的电子致密化专业化可能为这些不同过程的空间协调提供分子平台。为了研究该假设,我们检查了由电子断层扫描产生的秀丽隐杆线虫胆碱能神经肌肉接头的高分辨率三维模型。首先,我们发现SV通过类似于脊椎动物中描述的细丝在布顿内相互连接。其次,我们解决了以AZ为中心的密集投影的三维结构。密集的投影是一个比以前预期的结构更复杂的结构,细丝从核心结构中辐射出来,直接接触到布顿内部的SV和停靠在质膜上的SV。第三,我们通过分析破坏两个关键AZ蛋白的突变体(UNC-10 / RIM和SYD-2 / liprin),研究了这些接触的功能相关性。在这两个突变体中,SV与密集投影之间的接触数量显着减少。与unc-10突变体相似,与野生型相比,syd-2突变体加剧了SV融合对细胞外钙浓度的依赖性。因此,我们提出致密的投射可通过UNC-10 / RIM和SYD-2 /脂蛋白依赖性机制将初生囊泡保持在AZ上,从而确保初生囊泡与钙信号的正确偶联。

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