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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Visualization and trafficking of the vesicular acetylcholine transporter in living cholinergic cells.
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Visualization and trafficking of the vesicular acetylcholine transporter in living cholinergic cells.

机译:胆碱能细胞中水泡乙酰胆碱转运蛋白的可视化和运输。

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The present experiments investigated the trafficking of the vesicular acetylcholine transporter (VAChT) tagged with the enhanced green fluorescent protein (EGFP) in living cholinergic cells (SN56). The EGFP-VAChT chimera was located in endosomal-like compartments in the soma of SN56 cells, and it was also targeted to varicosities of neurites. In contrast, EGFP alone in cells was soluble in the cytoplasm. The C-terminal cytoplasmic tail of VAChT has been implicated in targeting of VAChT to synaptic vesicles; thus, we have examined the role of the C-terminal region in the trafficking to varicosities. A C-terminal fragment tagged with EGFP appeared to be selectively accumulated in varicosities when expressed in SN56 cells. Interestingly, the protein was not freely soluble in the cytosol, and it presented a punctate pattern of expression. However, EGFP-C terminus did not present this peculiar pattern of expression in a nonneuronal cell line (HEK 293). Moreover, the C-terminal region of VAChT did not seem to be essential for VAChT trafficking, as a construct that lacks the C-terminal tail was, similar to EGFP-VAChT, partially targeted to endocytic organelles in the soma and sorted to varicosities. These experiments visualize VAChT for the first time in living cells and suggest that there might be multiple signals that participate in trafficking of VAChT to sites of synaptic vesicle accumulation.
机译:本实验研究了在活胆碱能细胞(SN56)中标记有增强绿色荧光蛋白(EGFP)的水泡乙酰胆碱转运蛋白(VAChT)的运输。 EGFP-VAChT嵌合体位于SN56细胞体的内体样区室中,并且还针对神经突的曲张性。相反,仅细胞中的EGFP可溶于细胞质。 VAChT的C末端胞质尾端与VAChT靶向突触小泡有关。因此,我们研究了C末端区域在静脉曲张运输中的作用。当在SN56细胞中表达时,标记有EGFP的C端片段似乎选择性地聚集在静脉曲张中。有趣的是,该蛋白质不能自由地溶解在细胞质中,并且呈现出点状的表达模式。但是,EGFP-C末端在非神经元细胞系(HEK 293)中未呈现这种特殊的表达模式。此外,VAChT的C末端区域似乎对于VAChT贩运不是必需的,因为缺少C末端尾巴的构建体类似于EGFP-VAChT,部分靶向于体细胞中的内吞性细胞器并分类为静脉曲张。这些实验首次使活细胞中的VAChT可视化,并暗示可能有多个信号参与VAChT向突触小泡积累部位的运输。

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