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新生 APP 在海马神经元中的命运:一项活细胞成像研究。

The Fate of Nascent APP in Hippocampal Neurons: A Live Cell Imaging Study.

机构信息

Department of Pharmacology , Vanderbilt University , Nashville , Tennessee 37232-6600 , United States.

出版信息

ACS Chem Neurosci. 2018 Sep 19;9(9):2225-2232. doi: 10.1021/acschemneuro.8b00226. Epub 2018 Jun 21.

Abstract

Amyloid precursor protein (APP) is closely associated with Alzheimer's disease (AD) because its proteolytic products form amyloid plaques and its mutations are linked to familial AD patients. As a membrane protein, APP is involved in neuronal development and plasticity. However, it remains unclear how nascent APP is distributed and transported to designated membrane compartments to execute its diverse functions. Here, we employed a dual-tagged APP fusion protein in combination with a synaptic vesicle marker to study the surface trafficking and cleavage of APP in hippocampal neurons immediately after its synthesis. Using long-term time-lapse imaging, we found that a considerable amount of nascent APP was directly transported to the somatodendritic surface, from which it propagates to distal neurites. Some APP in the plasma membrane was endocytosed and some was cleaved by α-secretase. Hence, we conclude that surface transportation of APP is a major step preceding its proteolytic processing and neuritic distribution.

摘要

淀粉样前体蛋白 (APP) 与阿尔茨海默病 (AD) 密切相关,因为其蛋白水解产物形成淀粉样斑块,其突变与家族性 AD 患者有关。作为一种膜蛋白,APP 参与神经元的发育和可塑性。然而,目前尚不清楚新生的 APP 是如何分布和运输到指定的膜区室,以执行其多种功能。在这里,我们使用双标记的 APP 融合蛋白与突触小泡标记物结合,研究 APP 在海马神经元中的表面运输和切割,即在其合成后立即进行。通过长期延时成像,我们发现相当数量的新生 APP 被直接运输到树突状表面,从那里它传播到远端神经突。质膜中的一些 APP 被内吞,一些被 α-分泌酶切割。因此,我们得出结论,APP 的表面运输是其蛋白水解加工和神经突分布的主要步骤。

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