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Scribble Interacts with β-Catenin to Localize Synaptic Vesicles to Synapses

机译:涂鸦与β-连环蛋白相互作用,使突触小泡定位于突触。

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An understanding of how synaptic vesicles are recruited to and maintained at presynaptic compartments is required to discern the molecular mechanisms underlying presynaptic assembly and plasticity. We have previously demonstrated that cadherin–β-catenin complexes cluster synaptic vesicles at presynaptic sites. Here we show that scribble interacts with the cadherin–β-catenin complex to coordinate vesicle localization. Scribble and β-catenin are colocalized at synapses and can be coimmunoprecipitated from neuronal lysates, indicating an interaction between scribble and β-catenin at the synapse. Using an RNA interference approach, we demonstrate that scribble is important for the clustering of synaptic vesicles at synapses. Indeed, in scribble knockdown cells, there is a diffuse distribution of synaptic vesicles along the axon, and a deficit in vesicle recycling. Despite this, synapse number and the distribution of the presynaptic active zone protein, bassoon, remain unchanged. These effects largely phenocopy those observed after ablation of β -catenin . In addition, we show that loss of β-catenin disrupts scribble localization in primary neurons but that the localization of β-catenin is not dependent on scribble. Our data supports a model by which scribble functions downstream of β-catenin to cluster synaptic vesicles at developing synapses.
机译:需要了解如何将突触小泡募集并维持在突触前隔室中,以识别突触前组装和可塑性的分子机制。我们以前已经证明,钙粘蛋白-β-连环蛋白复合物在突触前位点聚集突触小泡。在这里,我们显示了涂鸦与钙粘蛋白-β-连环蛋白复合物相互作用,以协调囊泡的定位。涂鸦和β-连环蛋白在突触处共定位,并且可以从神经元裂解物中进行免疫共沉淀,表明涂鸦和β-连环蛋白在突触之间具有相互作用。使用RNA干扰方法,我们证明了涂抹对于突触中突触小泡的聚簇很重要。实际上,在杂种敲低的细胞中,突触小泡沿轴突分散分布,并且小泡再循环不足。尽管如此,突触数量和突触前活性区蛋白巴松的分布保持不变。这些作用主要是在消融β-catenin后观察到的。另外,我们表明,β-catenin的缺失会破坏原代神经元中的涂鸦位置,但是β-catenin的位置并不依赖于涂鸦。我们的数据支持一种模型,通过该模型,杂草在β-catenin的下游起作用,以在突触形成时将突触小泡聚集。

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