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多巴胺转运体通过一种通道机制使神经元去极化。

Dopamine transporters depolarize neurons by a channel mechanism.

作者信息

Carvelli Lucia, McDonald Paul W, Blakely Randy D, DeFelice Louis J

机构信息

Department of Pharmacology and Center of Neuroscience, Vanderbilt University School of Medicine, Nashville, TN 37232-8548, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):16046-51. doi: 10.1073/pnas.0403299101. Epub 2004 Nov 1.

Abstract

Neurotransmitter transporters generate larger currents than expected if one assumes fixed stoichiometry models. It remains controversial, however, whether these depolarizing currents arise from high density and rapid turnover rates of a classical transporter, or whether transporters exhibit bona fide channel behavior. Although heterologously expressed transporters show single-channel behavior and noise analysis in native cells strongly suggests channel behavior, no directly observed single-channel events associated with transporters have been reported thus far in native cells. We describe single-channel events arising directly from the Caenorhabditis elegans dopamine transporter (DAT-1) as evidenced by DA-induced channel activity blocked by a high-affinity DAT-1 inhibitor, increased channel activity in neurons that overexpress DAT-1, and loss of channels in dat-1 knockout neurons. Our data indicate that authentic transporter channels underlie depolarizing whole-cell currents. Thus, DA transporters not only transport DA but also exhibit a channel mode of conduction that directly modulates membrane potential and neuronal function.

摘要

如果假设固定化学计量模型,神经递质转运体产生的电流比预期的要大。然而,这些去极化电流是源于经典转运体的高密度和快速周转率,还是转运体表现出真正的通道行为,仍然存在争议。尽管异源表达的转运体显示出单通道行为,并且在天然细胞中的噪声分析强烈表明存在通道行为,但迄今为止,在天然细胞中尚未报道与转运体相关的直接观察到的单通道事件。我们描述了直接源自秀丽隐杆线虫多巴胺转运体(DAT-1)的单通道事件,证据包括:多巴胺诱导的通道活性被高亲和力DAT-1抑制剂阻断;在过表达DAT-1的神经元中通道活性增加;以及在dat-1基因敲除神经元中通道丧失。我们的数据表明,真正的转运体通道是去极化全细胞电流的基础。因此,多巴胺转运体不仅转运多巴胺,还表现出一种直接调节膜电位和神经元功能的通道传导模式。

相似文献

1
Dopamine transporters depolarize neurons by a channel mechanism.多巴胺转运体通过一种通道机制使神经元去极化。
Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):16046-51. doi: 10.1073/pnas.0403299101. Epub 2004 Nov 1.

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