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由 ATP 释放和高度脱敏的人 P2X1 受体维持的张力钙激活氯离子电流。

Tonic Calcium-Activated Chloride Current Sustained by ATP Release and Highly Desensitizing Human P2X1 Receptors.

机构信息

Department of Neurology, Mitchel Center for Neurodegenerative Diseases, School of Medicine, University of Texas Medical Branch at Galveston, USA; Department of Neurobiology and Behavior, School of Medicine, University of California Irvine, USA.

Department of Neurobiology and Behavior, School of Medicine, University of California Irvine, USA.

出版信息

Neuroscience. 2020 Jul 15;439:332-341. doi: 10.1016/j.neuroscience.2019.07.025. Epub 2019 Jul 23.

Abstract

Extracellular adenosine triphosphate (ATP) participates in maintaining the vascular tone in the CNS, particularly in the retina, via the tonic activity of ligand gated activated P2X1 receptors. P2X1 receptors are characterized by their high affinity for ATP and their strong desensitization to concentrations of ATP that are 200-fold lower than their EC. The mechanism behind P2X1 tonic activity remains unclear. In this study, we expressed human P2X1 (hP2X1) homomeric receptors in Xenopus oocytes to explore the relationship between ATP release from oocytes at rest, hP2X1, and Ca-activated Cl channels. Our results indicate that Xenopus oocytes release ATP at rest via vesicular exocytosis, and this process is a constitutive phenomenon independent of extracellular Ca. Our results also indicate that hP2X1 receptors are able to sustain a tonic activity of Ca-activated Cl channels. In the presence of extracellular Ca the activity of hP2X1 receptors is greatly amplified by its coupling with Ca-activated Cl channels. Future studies addressing the relationship between hP2X1 receptors and Ca-activated Cl channels in vascular smooth muscle cells should provide information about additional mechanisms that regulate the vascular tone and their potential as pharmaceutical targets. This article is part of a Special Issue entitled: Honoring Ricardo Miledi - outstanding neuroscientist of XX-XXI centuries.

摘要

细胞外三磷酸腺苷(ATP)通过配体门控激活的 P2X1 受体的紧张性活动参与中枢神经系统中血管张力的维持,特别是在视网膜中。P2X1 受体的特点是对 ATP 的高亲和力和对浓度为 EC 低 200 倍的 ATP 的强烈脱敏作用。P2X1 紧张性活动的背后机制尚不清楚。在这项研究中,我们在非洲爪蟾卵母细胞中表达了人 P2X1(hP2X1)同源受体,以探讨卵母细胞在休息时从卵母细胞中释放 ATP、hP2X1 和 Ca 激活的 Cl 通道之间的关系。我们的结果表明,非洲爪蟾卵母细胞通过囊泡胞吐作用在休息时释放 ATP,这一过程是一种独立于细胞外 Ca 的组成型现象。我们的结果还表明,hP2X1 受体能够维持 Ca 激活的 Cl 通道的紧张性活性。在存在细胞外 Ca 的情况下,hP2X1 受体的活性通过与 Ca 激活的 Cl 通道的偶联而大大放大。未来研究解决血管平滑肌细胞中 hP2X1 受体和 Ca 激活的 Cl 通道之间的关系,应该提供有关调节血管张力的其他机制的信息及其作为药物靶点的潜力。本文是一个题为“纪念 Ricardo Miledi-XX-XXI 世纪杰出神经科学家”的特刊的一部分。

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