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首页> 外文期刊>Alzheimer’s & dementia: the journal of the Alzheimer’s Association >Synaptic vesicle cycle and amyloid beta: Biting the hand that feeds
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Synaptic vesicle cycle and amyloid beta: Biting the hand that feeds

机译:突触囊泡循环和淀粉样蛋白β:咬住饲料的手

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摘要

The synaptic vesicle cycle (SVC) holds center stage in the biology of presynaptic terminals. Through recurrent exocytosis and endocytosis, it facilitates a sequence of events enabling chemical neurotransmission between functionally related neurons. As a fundamental process that links the interior of nerve cells with their environment, the SVC is also critical for signaling and provides an entry route for a range of pathogens and toxins, enabling detrimental effects. In Alzheimer's disease, the SVC is both the prime site of amyloid beta production and toxicity. In this study, we discuss the emerging evidence for physiological and pathological effects of A beta on various stages of the SVC, from postfusion membrane recovery to trafficking, docking, and priming of vesicles for fusion and transmitter release. Understanding of the mechanisms of A beta interaction with the SVC within the unifying calcium hypothesis of aging and Alzheimer's disease should further elucidate the fundamental biology of the presynaptic terminal and reveal novel therapeutic targets for Alzheimer's disease and other age-related dementias. (C) 2018 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
机译:突触囊泡循环(SVC)在突触前终端的生物学中保持中心阶段。通过复发性外尿精和内吞作用,促进了一系列事件,使功能相关的神经元之间的化学神经传递。作为将神经细胞内部与其环境联系起来的基本过程,SVC对于信号传导也至关重要,并为一系列病原体和毒素提供进入途径,从而实现有害影响。在阿尔茨海默病的疾病中,SVC是淀粉样蛋白β产生和毒性的主要部位。在这项研究中,我们讨论了β在SVC的各个阶段的生理和病理作用的新出现证据,从融合,对接和囊泡的贩运,对接和引发进行融合和变送器释放。理解在统一钙的假设中与SVC的β相互作用的机制应进一步阐明突触前末端的基本生物学,并揭示了阿尔茨海默病和其他与年龄相关的痴呆症的新疗法靶标。 (c)2018年Alzheimer的协会。由elsevier Inc.保留所有权利发布。

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