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Polarized sorting of the copper transporter ATP7B in neurons mediated by recognition of a dileucine signal by AP-1

机译:AP-1识别双亮氨酸信号介导的神经元中铜转运蛋白ATP7B的极化分选

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摘要

Neurons are highly polarized cells having distinct somatodendritic and axonal domains. Here we report that polarized sorting of the Cu2+ transporter ATP7B and the vesicle-SNARE VAMP4 to the somatodendritic domain of rat hippocampal neurons is mediated by recognition of dileucine-based signals in the cytosolic domains of the proteins by the sigma 1 subunit of the clathrin adaptor AP-1. Under basal Cu2+ conditions, ATP7B was localized to the trans-Golgi network (TGN) and the plasma membrane of the soma and dendrites but not the axon. Mutation of a dileucine-based signal in ATP7B or overexpression of a dominant-negative sigma 1 mutant resulted in nonpolarized distribution of ATP7B between the somatodendritic and axonal domains. Furthermore, addition of high Cu2+ concentrations, previously shown to reduce ATP7B incorporation into AP-1-containing clathrin-coated vesicles, caused loss of TGN localization and somatodendritic polarity of ATP7B. These findings support the notion of AP-1 as an effector of polarized sorting in neurons and suggest that altered polarity of ATP7B in polarized cell types might contribute to abnormal copper metabolism in the MEDNIK syndrome, a neurocutaneous disorder caused by mutations in the sigma 1A subunit isoform of AP-1.
机译:神经元是高度极化的细胞,具有明显的躯体树突状和轴突结构域。在这里我们报告说,Cu2 +转运蛋白ATP7B和囊泡-SNARE VAMP4对大鼠海马神经元的体树突状结构域的极化排序是由网格蛋白适配器的sigma 1亚基识别蛋白质中胞质域中基于亮氨酸的信号介导的AP-1。在基础Cu2 +条件下,ATP7B定位于反式高尔基网络(TGN)和体细胞的质膜和树突而不是轴突。 ATP7B中基于双亮氨酸的信号突变或显性负sigma 1突变体的过表达导致ATP7B在体树突状和轴突域之间发生非极化分布。此外,高浓度的Cu2 +的添加(先前显示可减少ATP7B掺入含有AP-1的网格蛋白包被的囊泡中的作用)导致TGN定位的丧失和ATP7B的体树突极性。这些发现支持AP-1作为神经元极化排序效应的概念,并表明极化细胞类型中ATP7B极性的改变可能导致MEDNIK综合征中的铜代谢异常,MEDNIK综合征是由sigma 1A亚基突变引起的神经皮肤疾病。 AP-1的同工型。

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