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在成熟的中枢突触中,神经连接蛋白Iβ和神经配蛋白定位于相对的膜上。

Neurexin Ibeta and neuroligin are localized on opposite membranes in mature central synapses.

作者信息

Berninghausen Otto, Rahman M Atiqur, Silva John-Paul, Davletov Bazbek, Hopkins Colin, Ushkaryov Yuri A

机构信息

Division of Cell and Molecular Biology, Imperial College London, London, UK.

出版信息

J Neurochem. 2007 Dec;103(5):1855-63. doi: 10.1111/j.1471-4159.2007.04918.x. Epub 2007 Sep 13.

Abstract

Synaptogenesis requires formation of trans-synaptic complexes between neuronal cell-adhesion receptors. Heterophilic receptor pairs, such as neurexin Ibeta and neuroligin, can mediate distinct intracellular signals and form different cytoplasmic scaffolds in the pre- and post-synaptic neuron, and may be particularly important for synaptogenesis. However, the functions of neurexin and neuroligin depend on their distribution in the synapse. Neuroligin has been experimentally assigned to the post-synaptic membrane, while the localization of neurexin remains unclear. To study the subcellular distribution of neurexin Ibeta and neuroligin in mature cerebrocortical synapses, we have developed a novel method for the physical separation of junctional membranes and their direct analysis by western blotting. Using urea and dithiothreitol, we disrupted trans-synaptic protein links, without dissolving the lipid phase, and fractionated the pre- and post-synaptic membranes. The purity of these fractions was validated by electron microscopy and western blotting using multiple synaptic markers. A quantitative analysis has confirmed that neuroligin is localized strictly in the post-synaptic membrane. We have also demonstrated that neurexin Ibeta is largely (96%) pre-synaptic. Thus, neurexin Ibeta and neuroligin normally form trans-synaptic complexes and can transduce bidirectional signals.

摘要

突触形成需要神经元细胞粘附受体之间形成跨突触复合物。异嗜性受体对,如神经连接蛋白Iβ和神经配蛋白,可介导不同的细胞内信号,并在突触前和突触后神经元中形成不同的细胞质支架,这可能对突触形成尤为重要。然而,神经连接蛋白和神经配蛋白的功能取决于它们在突触中的分布。神经配蛋白已通过实验确定位于突触后膜,而神经连接蛋白的定位仍不清楚。为了研究神经连接蛋白Iβ和神经配蛋白在成熟大脑皮质突触中的亚细胞分布,我们开发了一种新方法,用于物理分离连接膜并通过蛋白质印迹法对其进行直接分析。我们使用尿素和二硫苏糖醇破坏跨突触蛋白连接,而不溶解脂质相,从而分离出突触前膜和突触后膜。通过电子显微镜和使用多种突触标记物的蛋白质印迹法验证了这些组分的纯度。定量分析证实神经配蛋白严格定位于突触后膜。我们还证明神经连接蛋白Iβ主要(96%)位于突触前。因此,神经连接蛋白Iβ和神经配蛋白通常形成跨突触复合物并可转导双向信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81b0/2517655/06e8147f786e/ukmss-2213-f0001.jpg

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