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突触前 DLG 通过定位电压激活的 Ca(2+) 通道调节突触功能。

Presynaptic DLG regulates synaptic function through the localization of voltage-activated Ca(2+) Channels.

机构信息

Biomedical Neuroscience Institute, Faculty of Medicine, Universidad de Chile, Santiago, Chile.

Program of Physiology and Biophysics, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.

出版信息

Sci Rep. 2016 Aug 30;6:32132. doi: 10.1038/srep32132.

Abstract

The DLG-MAGUK subfamily of proteins plays a role on the recycling and clustering of glutamate receptors (GLUR) at the postsynaptic density. discs-large1 (dlg) is the only DLG-MAGUK gene in Drosophila and originates two main products, DLGA and DLGS97 which differ by the presence of an L27 domain. Combining electrophysiology, immunostaining and genetic manipulation at the pre and postsynaptic compartments we study the DLG contribution to the basal synaptic-function at the Drosophila larval neuromuscular junction. Our results reveal a specific function of DLGS97 in the regulation of the size of GLUR fields and their subunit composition. Strikingly the absence of any of DLG proteins at the presynaptic terminal disrupts the clustering and localization of the calcium channel DmCa1A subunit (Cacophony), decreases the action potential-evoked release probability and alters short-term plasticity. Our results show for the first time a crucial role of DLG proteins in the presynaptic function in vivo.

摘要

DLG-MAGUK 蛋白家族在谷氨酸受体(GLUR)在突触后密度的再循环和聚集中发挥作用。 discs-large1 (dlg) 是果蝇中唯一的 DLG-MAGUK 基因,它产生两种主要产物,DLGA 和 DLGS97,它们的区别在于存在 L27 结构域。我们通过在突触前和突触后隔室进行电生理学、免疫染色和遗传操作,研究 DLG 对果蝇幼虫神经肌肉接头基础突触功能的贡献。我们的结果揭示了 DLGS97 在调节 GLUR 场大小及其亚基组成方面的特定功能。引人注目的是,在突触前末端缺乏任何 DLG 蛋白会破坏钙通道 DmCa1A 亚基(嘈杂)的聚类和定位,降低动作电位诱发的释放概率,并改变短期可塑性。我们的结果首次表明 DLG 蛋白在体内突触前功能中起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd68/5004195/ece19d777597/srep32132-f1.jpg

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