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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Piccolo regulates the dynamic assembly of presynaptic F-actin.
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Piccolo regulates the dynamic assembly of presynaptic F-actin.

机译:Piccolo调节突触前F-肌动蛋白的动态组装。

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Filamentous (F)-actin is a known regulator of the synaptic vesicle (SV) cycle, with roles in SV mobilization, fusion, and endocytosis. However, the molecular pathways that regulate its dynamic assembly within presynaptic boutons remain unclear. In this study, we have used shRNA-mediated knockdown to demonstrate that Piccolo, a multidomain protein of the active zone cytomatrix, is a key regulator of presynaptic F-actin assembly. Boutons lacking Piccolo exhibit enhanced activity-dependent Synapsin1a dispersion and SV exocytosis, and reduced F-actin polymerization and CaMKII recruitment. These phenotypes are rescued by stabilizing F-actin filaments and mimicked by knocking down Profilin2, another regulator of presynaptic F-actin assembly. Importantly, we find that mice with a targeted deletion of exon 14 from the Pclo gene, reported to lack >95% of Piccolo, continue to express multiple Piccolo isoforms. Furthermore, neurons cultured from these mice exhibit no defects in presynaptic F-actin assembly due to the expression of these isoforms at presynaptic boutons. These data reveal that Piccolo regulates neurotransmitter release by facilitating activity-dependent F-actin assembly and the dynamic recruitment of key signaling molecules into presynaptic boutons, and highlight the need for new genetic models with which to study Piccolo loss of function.
机译:丝状肌动蛋白是突触小泡(SV)周期的已知调节剂,在SV动员,融合和内吞作用中起作用。然而,尚不清楚调节突触前按钮内其动态组装的分子途径。在这项研究中,我们已使用shRNA介导的敲低来证明Piccolo(活性区细胞基质的多域蛋白)是突触前F-肌动蛋白装配的关键调节剂。缺少短笛的Boutons表现出增强的活性依赖性Synapsin1a分散和SV胞吐作用,并减少了F-肌动蛋白聚合和CaMKII募集。通过稳定F-肌动蛋白丝来挽救这些表型,并通过敲除突触前F-肌动蛋白装配的另一种调节剂Profilin2进行模拟。重要的是,我们发现具有从Pclo基因中靶向缺失外显子14的小鼠(据报道缺乏Piccolo的> 95%)继续表达多种Piccolo亚型。此外,从这些小鼠培养的神经元在突触前F-肌动蛋白组装中没有缺陷,这是由于这些同工型在突触前纽扣上的表达。这些数据表明,短笛通过促进依赖于活性的F-肌动蛋白装配和将关键信号分子动态募集到突触前的突触中来调节神经递质的释放,并强调需要新的遗传模型来研究短笛的功能丧失。

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