4.6 Article

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

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 295, Issue 16, Pages 5192-5203

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.RA119.010699

Keywords

ATP; ion channel; high-throughput screening (HTS); ABC transporter; cholesterol; ATP-binding cassette subfamily G member 1 (ABCG1); genome-wide ORF screen; hypotonic shock; neurotransmission; volume-regulated anion channel (VRAC)

Funding

  1. National Institute of Health from NINDS [RC1 NS068966]
  2. National Institute of Health from NIMH [U01 MH104984]
  3. NIGMS, National Institutes of Health Predoctoral Pharmacology Training Program [T32-GM007324]
  4. National Institutes of Health Cellular and Molecular Biology Training Grant [T32-GM007223]
  5. National Institutes of Health Neurobiology of Cortical Systems Training Grant [T32-GNS007224]
  6. Yale University
  7. Gruber Foundation
  8. Kavli Foundation

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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.

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