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ABC 转运蛋白通过胆固醇依赖性体积调节阴离子通道活性控制 ATP 的释放。

ABC transporters control ATP release through cholesterol-dependent volume-regulated anion channel activity.

机构信息

Department of Cellular and Molecular Physiology, Department of Neuroscience, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale Kavli Institute, Yale University School of Medicine, New Haven, Connecticut 06520.

Department of Cellular and Molecular Physiology, Department of Neuroscience, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale Kavli Institute, Yale University School of Medicine, New Haven, Connecticut 06520.

出版信息

J Biol Chem. 2020 Apr 17;295(16):5192-5203. doi: 10.1074/jbc.RA119.010699. Epub 2020 Jan 27.

Abstract

Purinergic signaling by extracellular ATP regulates a variety of cellular events and is implicated in both normal physiology and pathophysiology. Several molecules have been associated with the release of ATP and other small molecules, but their precise contributions have been difficult to assess because of their complexity and heterogeneity. Here, we report on the results of a gain-of-function screen for modulators of hypotonicity-induced ATP release using HEK-293 cells and murine cerebellar granule neurons, along with bioluminescence, calcium FLIPR, and short hairpin RNA-based gene-silencing assays. This screen utilized the most extensive genome-wide ORF collection to date, covering 90% of human, nonredundant, protein-encoding genes. We identified two ABCG1 (ABC subfamily G member 1) variants, which regulate cellular cholesterol, as modulators of hypotonicity-induced ATP release. We found that cholesterol levels control volume-regulated anion channel-dependent ATP release. These findings reveal novel mechanisms for the regulation of ATP release and volume-regulated anion channel activity and provide critical links among cellular status, cholesterol, and purinergic signaling.

摘要

细胞外 ATP 通过嘌呤能信号转导调节各种细胞事件,与正常生理和病理生理都有关联。有几种分子与 ATP 和其他小分子的释放有关,但由于其复杂性和异质性,它们的确切贡献一直难以评估。在这里,我们报告了使用 HEK-293 细胞和鼠小脑颗粒神经元进行的针对低渗诱导的 ATP 释放的功能获得性筛选的结果,以及生物发光、钙 FLIPR 和短发夹 RNA 基基因沉默测定。该筛选利用了迄今为止最广泛的全基因组 ORF 集合,涵盖了 90%的人类、非冗余、蛋白质编码基因。我们鉴定了两种 ABCG1(ABC 亚家族 G 成员 1)变体,它们调节细胞胆固醇,是低渗诱导的 ATP 释放的调节剂。我们发现胆固醇水平控制体积调节阴离子通道依赖性 ATP 释放。这些发现揭示了调节 ATP 释放和体积调节阴离子通道活性的新机制,并为细胞状态、胆固醇和嘌呤能信号之间提供了关键联系。

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